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1
Larkum, M. E., M. G. Rioult, and H. R. Luscher. "Propagation of action potentials in the dendrites of neurons from rat spinal cord slice cultures." Journal of Neurophysiology 75, no. 1 (January 1, 1996): 154–70. http://dx.doi.org/10.1152/jn.1996.75.1.154.
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1. We examined the propagation of action potentials in the dendrites of ventrally located presumed motoneurons of organotypic rat spinal cord cultures. Simultaneous patch electrode recordings were made from the dendrites and somata of individual cells. In other experiments we visualized the membrane voltage over all the proximal dendrites simultaneously using a voltage-sensitive dye and an array of photodiodes. Calcium imaging was used to measure the dendritic rise in Ca2+ accompanying the propagating action potentials. 2. Spontaneous and evoked action potentials were recorded using high-resistance patch electrodes with separations of 30-423 microm between the somatic and dendritic electrodes. 3. Action potentials recorded in the dendrites varied considerably in amplitude but were larger than would be expected if the dendrites were to behave as passive cables (sometimes little or no decrement was seen for distances of > 100 microm). Because the amplitude of the action potentials in different dendrites was not a simple function of distance from the soma, we suggest that the conductance responsible for the boosting of the action potential amplitude varied in density from dendrite to dendrite and possibly along each dendrite. 4. The dendritic action potentials were usually smaller and broader and arrived later at the dendritic electrode than at the somatic electrode irrespective of whether stimulation occurred at the dendrite or soma or as a result of spontaneous synaptic activity. This is clear evidence that the action potential is initiated at or near the soma and spreads out into the dendrites. The conduction velocity of the propagating action potential was estimated to be 0.5 m/s. 5. The voltage time courses of previously recorded action potentials were generated at the soma using voltage clamp before and after applying 1 microM tetrodotoxin (TTX) over the soma and dendrites. TTX reduced the amplitude of the action potential at the dendritic electrode to a value in the range expected for dendrites that behave as passive cables. This indicates that the conductance responsible for the actively propagating action potentials is a Na+ conductance. 6. The amplitude of the dendritic action potential could also be initially reduced more than the somatic action potential using 1-10 mM QX-314 (an intracellular sodium channel blocker) in the dendritic electrode as the drug diffused from the dendritic electrode toward the soma. Furthermore, in some cases the action potential elicited by current injection into the dendrite had two components. The first component was blocked by QX-314 in the first few seconds of the diffusion of the blocker. 7. In some cells, an afterdepolarizing potential (ADP) was more prominent in the dendrite than in the soma. This ADP could be reversibly blocked by 1 mM Ni2+ or by perfusion of a nominally Ca2+-free solution over the soma and dendrites. This suggests that the back-propagating action potential caused an influx of Ca2+ predominantly in the dendrites. 8. With the use of a voltage-sensitive dye (di-8-ANEPPS) and an array of photodiodes, the action potential was tracked along all the proximal dendrites simultaneously. The results confirmed that the action potential propagated actively, in contrast to similarly measured hyperpolarizing pulses that spread passively. There were also indications that the action potential was not uniformly propagated in all the dendrites, suggesting the possibility that the distribution of Na+ channels over the dendritic membrane is not uniform. 9. Calcium imaging with the Ca2+ fluorescent indicator Fluo-3 showed a larger percentage change in fluorescence in the dendrites than in the soma. Both bursts and single action potentials elicited sharp rises in fluorescence in the proximal dendrites, suggesting that the back-propagating action potential causes a concomitant rise in intracellular calcium concentration...
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Fujishima, Kazuto, Junko Kurisu, Midori Yamada, and Mineko Kengaku. "βIII spectrin controls the planarity of Purkinje cell dendrites by modulating perpendicular axon-dendrite interactions." Development 147, no. 24 (November 24, 2020): dev194530. http://dx.doi.org/10.1242/dev.194530.
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ABSTRACTThe mechanism underlying the geometrical patterning of axon and dendrite wiring remains elusive, despite its crucial importance in the formation of functional neural circuits. The cerebellar Purkinje cell (PC) arborizes a typical planar dendrite, which forms an orthogonal network with granule cell (GC) axons. By using electrospun nanofiber substrates, we reproduce the perpendicular contacts between PC dendrites and GC axons in culture. In the model system, PC dendrites show a preference to grow perpendicularly to aligned GC axons, which presumably contribute to the planar dendrite arborization in vivo. We show that βIII spectrin, a causal protein for spinocerebellar ataxia type 5, is required for the biased growth of dendrites. βIII spectrin deficiency causes actin mislocalization and excessive microtubule invasion in dendritic protrusions, resulting in abnormally oriented branch formation. Furthermore, disease-associated mutations affect the ability of βIII spectrin to control dendrite orientation. These data indicate that βIII spectrin organizes the mouse dendritic cytoskeleton and thereby regulates the oriented growth of dendrites with respect to the afferent axons.
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Mitchell, Josephine W., Ipek Midillioglu, Ethan Schauer, Bei Wang, Chun Han, and Jill Wildonger. "Coordination of Pickpocket ion channel delivery and dendrite growth in Drosophila sensory neurons." PLOS Genetics 19, no. 11 (November 9, 2023): e1011025. http://dx.doi.org/10.1371/journal.pgen.1011025.
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Sensory neurons enable an organism to perceive external stimuli, which is essential for survival. The sensory capacity of a neuron depends on the elaboration of its dendritic arbor and the localization of sensory ion channels to the dendritic membrane. However, it is not well understood when and how ion channels localize to growing sensory dendrites and whether their delivery is coordinated with growth of the dendritic arbor. We investigated the localization of the DEG/ENaC/ASIC ion channel Pickpocket (Ppk) in the peripheral sensory neurons of developing fruit flies. We used CRISPR-Cas9 genome engineering approaches to tag endogenous Ppk1 and visualize it live, including monitoring Ppk1 membrane localization via a novel secreted split-GFP approach. Fluorescently tagged endogenous Ppk1 localizes to dendrites, as previously reported, and, unexpectedly, to axons and axon terminals. In dendrites, Ppk1 is present throughout actively growing dendrite branches and is stably integrated into the neuronal cell membrane during the expansive growth of the arbor. Although Ppk channels are dispensable for dendrite growth, we found that an over-active channel mutant severely reduces dendrite growth, likely by acting at an internal membrane and not the dendritic membrane. Our data reveal that the molecular motor dynein and recycling endosome GTPase Rab11 are needed for the proper trafficking of Ppk1 to dendrites. Based on our data, we propose that Ppk channel transport is coordinated with dendrite morphogenesis, which ensures proper ion channel density and distribution in sensory dendrites.
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Christie, J. M., and G. L. Westbrook. "Regulation of Backpropagating Action Potentials in Mitral Cell Lateral Dendrites by A-Type Potassium Currents." Journal of Neurophysiology 89, no. 5 (May 1, 2003): 2466–72. http://dx.doi.org/10.1152/jn.00997.2002.
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Dendrodendritic synapses, distributed along mitral cell lateral dendrites, provide powerful and extensive inhibition in the olfactory bulb. Activation of inhibition depends on effective penetration of action potentials into dendrites. Although action potentials backpropagate with remarkable fidelity in apical dendrites, this issue is controversial for lateral dendrites. We used paired somatic and dendritic recordings to measure action potentials in proximal dendritic segments (0–200 μm from soma) and action potential-generated calcium transients to monitor activity in distal dendritic segments (200–600 μm from soma). Somatically elicited action potentials were attenuated in proximal lateral dendrites. The attenuation was not due to impaired access resistance in dendrites or to basal synaptic activity. However, a single somatically elicited action potential was sufficient to evoke a calcium transient throughout the lateral dendrite, suggesting that action potentials reach distal dendritic compartments. Block of A-type potassium channels ( I A) with 4-aminopyridine (10 mM) prevented action potential attenuation in direct recordings and significantly increased dendritic calcium transients, particularly in distal dendritic compartments. Our results suggest that I A may regulate inhibition in the olfactory bulb by controlling action potential amplitudes in lateral dendrites.
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Göbel, Werner, and Fritjof Helmchen. "New Angles on Neuronal Dendrites In Vivo." Journal of Neurophysiology 98, no. 6 (December 2007): 3770–79. http://dx.doi.org/10.1152/jn.00850.2007.
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Imaging technologies are well suited to study neuronal dendrites, which are key elements for synaptic integration in the CNS. Dendrites are, however, frequently oriented perpendicular to tissue surfaces, impeding in vivo imaging approaches. Here we introduce novel laser-scanning modes for two-photon microscopy that enable in vivo imaging of spatiotemporal activity patterns in dendrites. First, we developed a method to image planes arbitrarily oriented in 3D, which proved particularly beneficial for calcium imaging of parallel fibers and Purkinje cell dendrites in rat cerebellar cortex. Second, we applied free linescans—either through multiple dendrites or along a single vertically oriented dendrite—to reveal fast dendritic calcium dynamics in neocortical pyramidal neurons. Finally, we invented a ribbon-type 3D scanning method for imaging user-defined convoluted planes enabling simultaneous measurements of calcium signals along multiple apical dendrites. These novel scanning modes will facilitate optical probing of dendritic function in vivo.
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Feng, Chengye, Pankajam Thyagarajan, Matthew Shorey, Dylan Y. Seebold, Alexis T. Weiner, Richard M. Albertson, Kavitha S. Rao, Alvaro Sagasti, Daniel J. Goetschius, and Melissa M. Rolls. "Patronin-mediated minus end growth is required for dendritic microtubule polarity." Journal of Cell Biology 218, no. 7 (May 10, 2019): 2309–28. http://dx.doi.org/10.1083/jcb.201810155.
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Microtubule minus ends are thought to be stable in cells. Surprisingly, in Drosophila and zebrafish neurons, we observed persistent minus end growth, with runs lasting over 10 min. In Drosophila, extended minus end growth depended on Patronin, and Patronin reduction disrupted dendritic minus-end-out polarity. In fly dendrites, microtubule nucleation sites localize at dendrite branch points. Therefore, we hypothesized minus end growth might be particularly important beyond branch points. Distal dendrites have mixed polarity, and reduction of Patronin lowered the number of minus-end-out microtubules. More strikingly, extra Patronin made terminal dendrites almost completely minus-end-out, indicating low Patronin normally limits minus-end-out microtubules. To determine whether minus end growth populated new dendrites with microtubules, we analyzed dendrite development and regeneration. Minus ends extended into growing dendrites in the presence of Patronin. In sum, our data suggest that Patronin facilitates sustained microtubule minus end growth, which is critical for populating dendrites with minus-end-out microtubules.
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Nithianandam, Vanitha, and Cheng-Ting Chien. "Actin blobs prefigure dendrite branching sites." Journal of Cell Biology 217, no. 10 (July 24, 2018): 3731–46. http://dx.doi.org/10.1083/jcb.201711136.
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The actin cytoskeleton provides structural stability and adaptability to the cell. Neuronal dendrites frequently undergo morphological changes by emanating, elongating, and withdrawing branches. However, the knowledge about actin dynamics in dendrites during these processes is limited. By performing in vivo imaging of F-actin markers, we found that F-actin was highly dynamic and heterogeneously distributed in dendritic shafts with enrichment at terminal dendrites. A dynamic F-actin population that we named actin blobs propagated bidirectionally at an average velocity of 1 µm/min. Interestingly, these actin blobs stalled at sites where new dendrites would branch out in minutes. Overstabilization of F-actin by the G15S mutant abolished actin blobs and dendrite branching. We identified the F-actin–severing protein Tsr/cofilin as a regulator of dynamic actin blobs and branching activity. Hence, actin blob localization at future branching sites represents a dendrite-branching mechanism to account for highly diversified dendritic morphology.
8
Schiller, Yitzhak. "Inter-Ictal- and Ictal-Like Epileptic Discharges in the Dendritic Tree of Neocortical Pyramidal Neurons." Journal of Neurophysiology 88, no. 6 (December 1, 2002): 2954–62. http://dx.doi.org/10.1152/jn.00525.2001.
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Dendritic mechanisms have been implied to play a key role in the formation of epileptic discharges. However, presently only a handful of direct dendritic recordings have been reported during epileptic discharges. In this study, I performed simultaneous voltage recordings from the soma and apical dendrite of the same neuron combined with calcium-imaging measurements to investigate inter-ictal- and ictal-like epileptic discharges in dendrites of layer 5 pyramidal neurons. Neocortical brain slices treated with bicuculline (BCC) produced both isolated “inter-ictal” paroxysymal depolarization shift (PDS) responses and electrographic seizures. Concomitant voltage recordings from the soma and apical dendrite revealed that PDS responses developed in both the apical dendrites and soma. However, the two responses differed from one another. In apical dendrites, the PDS was significantly higher in amplitude and shorter in duration compared with the somatic PDS. The PDS response in dendrites had a peak amplitude of 68.9 ± 2.2 (SD) mV, peak voltage value of 9.3 ± 2.7 mV, and half-width of 203.8 ± 38.4 ms. In contrast, the somatic PDS had a peak amplitude of 48.7 ± 2.7 mV, peak voltage value of −11.9 ± 3.1 mV, and half-width of 247.8 ± 57.3 ms ( P < 0.01, n = 18). In addition the apical dendritic PDS always preceded the somatic counterpart in all 18 neurons examined. Concomitant calcium-imaging measurements showed the PDS evoked large calcium influx into the entire dendritic tree including the apical tuft, basal, and oblique dendrites. The PDS evoked [Ca2+]i were not uniform along the dendritic tree, being highest in the oblique dendrites (71.3 ± 14.5 μM) and lowest at the distal tuft branches (9.3 ± 0.7 μM). The PDS responses persisted after blockade of voltage-gated sodium channels by intracellular QX-314 but became narrower (by 69.6 ± 9.7%) following intracellular administration of the voltage-gated calcium channel blocker D600. Electrographic seizures recorded in the soma and apical dendrites were composed of recurrent bursts. The initial bursts represented PDS responses. During the seizure the amplitude of bursts gradually attenuated and reached an average value of 26 ± 13% of the initial ictal PDS burst. Double recordings during electrographic seizures revealed the initial one to four ictal bursts appeared first at the apical dendrite while later ictal bursts were always observed first at the soma. In conclusion, the results of this study show “inter-ictal” PDS responses originated in the apical dendritic tree, were partially mediated by voltage-gated calcium channels and spread throughout the dendritic tree including the fine tuft, basal, and oblique dendrites. During electrographic seizures the origin of epileptic bursts shifted from the apical dendritic tree to the soma-basal region.
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Sharp, D. J., W. Yu, and P. W. Baas. "Transport of dendritic microtubules establishes their nonuniform polarity orientation." Journal of Cell Biology 130, no. 1 (July 1, 1995): 93–103. http://dx.doi.org/10.1083/jcb.130.1.93.
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The immature processes that give rise to both axons and dendrites contain microtubules (MTs) that are uniformly oriented with their plus-ends distal to the cell body, and this pattern is preserved in the developing axon. In contrast, developing dendrites gradually acquire nonuniform MT polarity orientation due to the addition of a subpopulation of oppositely oriented MTs (Baas, P. W., M. M. Black, and G. A. Banker. 1989. J. Cell Biol. 109:3085-3094). In theory, these minus-end-distal MTs could be locally nucleated and assembled within the dendrite itself, or could be transported into the dendrite after their nucleation within the cell body. To distinguish between these possibilities, we exposed cultured hippocampal neurons to nanomolar levels of vinblastine after one of the immature processes had developed into the axon but before the others had become dendrites. At these levels, vinblastine acts as a kinetic stabilizer of MTs, inhibiting further assembly while not substantially depolymerizing existing MTs. This treatment did not abolish dendritic differentiation, which occurred in timely fashion over the next two to three days. The resulting dendrites were flatter and shorter than controls, but were identifiable by their ultrastructure, chemical composition, and thickened tapering morphology. The growth of these dendrites was accompanied by a diminution of MTs from the cell body, indicating a net transfer of MTs from one compartment into the other. During this time, minus-end-distal microtubules arose in the experimental dendrites, indicating that new MT assembly is not required for the acquisition of nonuniform MT polarity orientation in the dendrite. Minus-end-distal microtubules predominated in the more proximal region of experimental dendrites, indicating that most of the MTs at this stage of development are transported into the dendrite with their minus-ends leading. These observations indicate that transport of MTs from the cell body is an essential feature of dendritic development, and that this transport establishes the nonuniform polarity orientation of MTs in the dendrite.
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Velte, Toby J., and Richard H. Masland. "Action Potentials in the Dendrites of Retinal Ganglion Cells." Journal of Neurophysiology 81, no. 3 (March 1, 1999): 1412–17. http://dx.doi.org/10.1152/jn.1999.81.3.1412.
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Action potentials in the dendrites of retinal ganglion cells. The somas and dendrites of intact retinal ganglion cells were exposed by enzymatic removal of the overlying endfeet of the Müller glia. Simultaneous whole cell patch recordings were made from a ganglion cell’s dendrite and the cell’s soma. When a dendrite was stimulated with depolarizing current, impulses often propagated to the soma, where they appeared as a mixture of small depolarizations and action potentials. When the soma was stimulated, action potentials always propagated back through the dendrite. The site of initiation of action potentials, as judged by their timing, could be shifted between soma and dendrite by changing the site of stimulation. Applying QX-314 to the soma could eliminate somatic action potentials while leaving dendritic impulses intact. The absolute amplitudes of the dendritic action potentials varied somewhat at different distances from the soma, and it is not clear whether these variations are real or technical. Nonetheless, the qualitative experiments clearly suggest that the dendrites of retinal ganglion cells generate regenerative Na+ action potentials, at least in response to large direct depolarizations.
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Lüscher, Hans-R., and Matthew E. Larkum. "Modeling Action Potential Initiation and Back-Propagation in Dendrites of Cultured Rat Motoneurons." Journal of Neurophysiology 80, no. 2 (August 1, 1998): 715–29. http://dx.doi.org/10.1152/jn.1998.80.2.715.
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Lüscher, Hans-R. and Matthew E. Larkum. Modeling action potential initiation and back-propagation in dendrites of cultured rat motoneurons. J. Neurophysiol. 80: 715–729, 1998. Regardless of the site of current injection, action potentials usually originate at or near the soma and propagate decrementally back into the dendrites. This phenomenon has been observed in neocortical pyramidal cells as well as in cultured motoneurons. Here we show that action potentials in motoneurons can be initiated in the dendrite as well, resulting in a biphasic dendritic action potential. We present a model of spinal motoneurons that is consistent with observed physiological properties of spike initiation in the initial segment/axon hillock region and action potential back-propagation into the dendritic tree. It accurately reproduces the results presented by Larkum et al. on motoneurons in organotypic rat spinal cord slice cultures. A high Na+-channel density of ḡ Na = 700 mS/cm2 at the axon hillock/initial segment region was required to secure antidromic invasion of the somato-dendritic membrane, whereas for the orthodromic direction, a Na+-channel density of ḡ Na = 1,200 mS/cm2 was required. A “weakly” excitable ( ḡ Na = 3 mS/cm2) dendritic membrane most accurately describes the experimentally observed attenuation of the back-propagated action potential. Careful analysis of the threshold conditions for action potential initiation at the initial segment or the dendrites revealed that, despite the lower voltage threshold for spike initiation in the initial segment, an action potential can be initiated in the dendrite before the initial segment fires a spike. Spike initiation in the dendrite depends on the passive cable properties of the dendritic membrane, its Na+-channel density, and local structural properties, mainly the diameter of the dendrites. Action potentials are initiated more easily in distal than in proximal dendrites. Whether or not such a dendritic action potential invades the soma with a subsequent initiation of a second action potential in the initial segment depends on the actual current source-load relation between the action potential approaching the soma and the electrical load of the soma together with the attached dendrites.
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Ligon, Cheryl, Eunju Seong, Ethan J. Schroeder, Nicholas W. DeKorver, Li Yuan, Tammy R. Chaudoin, Yu Cai, Shilpa Buch, Stephen J. Bonasera, and Jyothi Arikkath. "δ-Catenin engages the autophagy pathway to sculpt the developing dendritic arbor." Journal of Biological Chemistry 295, no. 32 (June 17, 2020): 10988–1001. http://dx.doi.org/10.1074/jbc.ra120.013058.
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The development of the dendritic arbor in pyramidal neurons is critical for neural circuit function. Here, we uncovered a pathway in which δ-catenin, a component of the cadherin–catenin cell adhesion complex, promotes coordination of growth among individual dendrites and engages the autophagy mechanism to sculpt the developing dendritic arbor. Using a rat primary neuron model, time-lapse imaging, immunohistochemistry, and confocal microscopy, we found that apical and basolateral dendrites are coordinately sculpted during development. Loss or knockdown of δ-catenin uncoupled this coordination, leading to retraction of the apical dendrite without altering basolateral dendrite dynamics. Autophagy is a key cellular pathway that allows degradation of cellular components. We observed that the impairment of the dendritic arbor resulting from δ-catenin knockdown could be reversed by knockdown of autophagy-related 7 (ATG7), a component of the autophagy machinery. We propose that δ-catenin regulates the dendritic arbor by coordinating the dynamics of individual dendrites and that the autophagy mechanism may be leveraged by δ-catenin and other effectors to sculpt the developing dendritic arbor. Our findings have implications for the management of neurological disorders, such as autism and intellectual disability, that are characterized by dendritic aberrations.
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Cazé, Romain D. "Any neuron can perform linearly non-separable computations." F1000Research 10 (July 6, 2021): 539. http://dx.doi.org/10.12688/f1000research.53961.1.
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Multiple studies have shown how dendrites enable some neurons to perform linearly non-separable computations. These works focus on cells with an extended dendritic arbor where voltage can vary independently, turning dendritic branches into local non-linear subunits. However, these studies leave a large fraction of the nervous system unexplored. Many neurons, e.g. granule cells, have modest dendritic trees and are electrically compact. It is impossible to decompose them into multiple independent subunits. Here, we upgraded the integrate and fire neuron to account for saturating dendrites. This artificial neuron has a unique membrane voltage and can be seen as a single layer. We present a class of linearly non-separable computations and how our neuron can perform them. We thus demonstrate that even a single layer neuron with dendrites has more computational capacity than without. Because any neuron has one or more layer, and all dendrites do saturate, we show that any dendrited neuron can implement linearly non-separable computations.
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Cazé, Romain D. "Any neuron can perform linearly non-separable computations." F1000Research 10 (September 16, 2021): 539. http://dx.doi.org/10.12688/f1000research.53961.2.
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Multiple studies have shown how dendrites enable some neurons to perform linearly non-separable computations. These works focus on cells with an extended dendritic arbor where voltage can vary independently, turning dendritic branches into local non-linear subunits. However, these studies leave a large fraction of the nervous system unexplored. Many neurons, e.g. granule cells, have modest dendritic trees and are electrically compact. It is impossible to decompose them into multiple independent subunits. Here, we upgraded the integrate and fire neuron to account for saturating dendrites. This artificial neuron has a unique membrane voltage and can be seen as a single layer. We present a class of linearly non-separable computations and how our neuron can perform them. We thus demonstrate that even a single layer neuron with dendrites has more computational capacity than without. Because any neuron has one or more layer, and all dendrites do saturate, we show that any dendrited neuron can implement linearly non-separable computations.
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Cook, Erik P., and Daniel Johnston. "Voltage-Dependent Properties of Dendrites That Eliminate Location-Dependent Variability of Synaptic Input." Journal of Neurophysiology 81, no. 2 (February 1, 1999): 535–43. http://dx.doi.org/10.1152/jn.1999.81.2.535.
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Voltage-dependent properties of dendrites that eliminate location-dependent variability of synaptic input. We examined the hypothesis that voltage-dependent properties of dendrites allow for the accurate transfer of synaptic information to the soma independent of synapse location. This hypothesis is motivated by experimental evidence that dendrites contain a complex array of voltage-gated channels. How these channels affect synaptic integration is unknown. One hypothesized role for dendritic voltage-gated channels is to counteract passive cable properties, rendering all synapses electrotonically equidistant from the soma. With dendrites modeled as passive cables, the effect a synapse exerts at the soma depends on dendritic location (referred to as location-dependent variability of the synaptic input). In this theoretical study we used a simplified three-compartment model of a neuron to determine the dendritic voltage-dependent properties required for accurate transfer of synaptic information to the soma independent of synapse location. A dendrite that eliminates location-dependent variability requires three components: 1) a steady-state, voltage-dependent inward current that together with the passive leak current provides a net outward current and a zero slope conductance at depolarized potentials, 2) a fast, transient, inward current that compensates for dendritic membrane capacitance, and 3) both αamino-3-hydroxy-5-methyl-4-isoxazolepropionic acid– and N-methyl-d-aspartate–like synaptic conductances that together permit synapses to behave as ideal current sources. These components are consistent with the known properties of dendrites. In addition, these results indicate that a dendrite designed to eliminate location-dependent variability also actively back-propagates somatic action potentials.
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Golding, Nace L., William L. Kath, and Nelson Spruston. "Dichotomy of Action-Potential Backpropagation in CA1 Pyramidal Neuron Dendrites." Journal of Neurophysiology 86, no. 6 (December 1, 2001): 2998–3010. http://dx.doi.org/10.1152/jn.2001.86.6.2998.
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In hippocampal CA1 pyramidal neurons, action potentials are typically initiated in the axon and backpropagate into the dendrites, shaping the integration of synaptic activity and influencing the induction of synaptic plasticity. Despite previous reports describing action-potential propagation in the proximal apical dendrites, the extent to which action potentials invade the distal dendrites of CA1 pyramidal neurons remains controversial. Using paired somatic and dendritic whole cell recordings, we find that in the dendrites proximal to 280 μm from the soma, single backpropagating action potentials exhibit <50% attenuation from their amplitude in the soma. However, in dendritic recordings distal to 300 μm from the soma, action potentials in most cells backpropagated either strongly (26–42% attenuation; n = 9/20) or weakly (71–87% attenuation; n = 10/20) with only one cell exhibiting an intermediate value (45% attenuation). In experiments combining dual somatic and dendritic whole cell recordings with calcium imaging, the amount of calcium influx triggered by backpropagating action potentials was correlated with the extent of action-potential invasion of the distal dendrites. Quantitative morphometric analyses revealed that the dichotomy in action-potential backpropagation occurred in the presence of only subtle differences in either the diameter of the primary apical dendrite or branching pattern. In addition, action-potential backpropagation was not dependent on a number of electrophysiological parameters (input resistance, resting potential, voltage sensitivity of dendritic spike amplitude). There was, however, a striking correlation of the shape of the action potential at the soma with its amplitude in the dendrite; larger, faster-rising, and narrower somatic action potentials exhibited more attenuation in the distal dendrites (300–410 μm from the soma). Simple compartmental models of CA1 pyramidal neurons revealed that a dichotomy in action-potential backpropagation could be generated in response to subtle manipulations of the distribution of either sodium or potassium channels in the dendrites. Backpropagation efficacy could also be influenced by local alterations in dendritic side branches, but these effects were highly sensitive to model parameters. Based on these findings, we hypothesize that the observed dichotomy in dendritic action-potential amplitude is conferred primarily by differences in the distribution, density, or modulatory state of voltage-gated channels along the somatodendritic axis.
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Yang, Luwei, Neng Ren, Jun Li, Mingxu Xia, Hongbiao Dong, and Jianguo Li. "Simulation of dendritic deformation induced by convection in alloy solidification." IOP Conference Series: Materials Science and Engineering 1281, no. 1 (May 1, 2023): 012038. http://dx.doi.org/10.1088/1757-899x/1281/1/012038.
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Abstract Dendritic deformation induced by convection of thermal fluid is one of the factors leading to dendrite fragmentation and plays a crucial role in grain structure of alloy, which lacks in-depth understanding. In this paper, we simulate the flow-induced mechanical deformation of dendrites during the solidification of Al-4.5wt.%Cu alloy by combining the cellular automaton-finite volume method (CA-FVM) for the dendrite growth and the finite element method (FEM) for handling the dendritic deformation with the complex boundary conditions given by CA-FVM results. It shows that the dendritic deformation strongly depends on the flow velocities of melt and dendritic morphology. The dendrites can undergo visible bending above the critical flow velocities for dendrite yield (ranging from 0.023 m/s to 0.126 m/s as the inlet velocity increases) and the von Mises stress increases as the flow is enhanced during the growth process.
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Grueber, Wesley B., Lily Y. Jan, and Yuh Nung Jan. "Tiling of the Drosophila epidermis by multidendritic sensory neurons." Development 129, no. 12 (June 15, 2002): 2867–78. http://dx.doi.org/10.1242/dev.129.12.2867.
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Insect dendritic arborization (da) neurons provide an opportunity to examine how diverse dendrite morphologies and dendritic territories are established during development. We have examined the morphologies of Drosophila da neurons by using the MARCM (mosaic analysis with a repressible cell marker) system. We show that each of the 15 neurons per abdominal hemisegment spread dendrites to characteristic regions of the epidermis. We place these neurons into four distinct morphological classes distinguished primarily by their dendrite branching complexities. Some class assignments correlate with known proneural gene requirements as well as with central axonal projections. Our data indicate that cells within two morphological classes partition the body wall into distinct, non-overlapping territorial domains and thus are organized as separate tiled sensory systems. The dendritic domains of cells in different classes, by contrast, can overlap extensively. We have examined the cell-autonomous roles of starry night (stan) (also known as flamingo (fmi)) and sequoia (seq) in tiling. Neurons with these genes mutated generally terminate their dendritic fields at normal locations at the lateral margin and segment border, where they meet or approach the like dendrites of adjacent neurons. However, stan mutant neurons occasionally send sparsely branched processes beyond these territories that could potentially mix with adjacent like dendrites. Together, our data suggest that widespread tiling of the larval body wall involves interactions between growing dendritic processes and as yet unidentified signals that allow avoidance by like dendrites.
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Ybarra, Natividad, Peter J. Hemond, Michael P. O'Boyle, and Kelly J. Suter. "Spatially Selective, Testosterone-Independent Remodeling of Dendrites in Gonadotropin-Releasing Hormone (GnRH) Neurons Prepubertally in Male Rats." Endocrinology 152, no. 5 (February 22, 2011): 2011–19. http://dx.doi.org/10.1210/en.2010-0871.
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Adult GnRH neurons exhibit a stereotypic morphology with a small soma, single axon, and single dendrite arising from the soma with little branching. The adult morphology of GnRH neurons in mice reflects an anatomical consolidation of dendrites over postnatal development. We examined this issue in rat GnRH neurons with biocytin filling in live hypothalamic slices from infant males, as adult littermates and in gonad-intact males, castrated males, and in males with one of three levels of testosterone (T) treatment. Somatic area and total dendritic length were significantly greater in infant males than in adults. Moreover, total numbers of dendrite branches were greater in infant males as compared with adults. The number of higher order branches and the lengths of higher order branches were also greater in infant males than in adults. Most interestingly, in adults a single dendrite arose from the somata, consistently at 180° from the axon. In contrast, prepubertal animals had an average of 2.2 ± 0.2 primary dendrites arising from somata (range, one to seven primary dendrites). Angles relative to the axon at which dendrites in prepubertal males emanated from GnRH somata were highly variable. Castration at 25 d of age and castration at 25 d of age with one of three levels of T treatment did not influence morphological parameters when GnRH neurons were examined between 40 d and 48 d of age. Thus, a spatially selective remodeling of primary dendrites and consolidation of distal GnRH dendritic arbors occurs during postnatal development and is largely independent of T.
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Chen, Ming, Yu Jiang, Wen Long Sun, Xiao Dong Hu, and Chun Li Liu. "Numerical Simulation of Binary Alloy Crystal Growth of Multiple Dendrites and Direcitonal Solidification Using Phase-Field Method." Advanced Materials Research 774-776 (September 2013): 703–6. http://dx.doi.org/10.4028/www.scientific.net/amr.774-776.703.
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Phase field method (PFM) offers the prospect of carrying out realistic numerical calculation on dendrite growth in metallic systems. The dendritic growth process of multiple dendrites and direcitonal solidification during isothermal solidifications in a Fe-0.5mole%C binary alloy were simulated using phase field model. Competitive growth of multiple equiaxed dendrites were simulated, and the effect of anisotropy on the solute segregation and microstructural dedritic growth pattern in directional solidification process was studied in the paper. The simulation results showed the impingement of arbitrarily oriented grains, and the grains began to impinge and coalesce the adjacent grains with time going on, which made the dendrite growth inhibited obviously. In the directional solidification, the maximum concentration gradient showed in the dendrite tip, and highest solute concentration existed at the bottom of the dendrites. With the increasing of the anisotropy, dendrite tip radius became smaller, and the crystal structure is more uniform and dense.
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Kelliher, Michael T., Yang Yue, Ashley Ng, Daichi Kamiyama, Bo Huang, Kristen J. Verhey, and Jill Wildonger. "Autoinhibition of kinesin-1 is essential to the dendrite-specific localization of Golgi outposts." Journal of Cell Biology 217, no. 7 (May 4, 2018): 2531–47. http://dx.doi.org/10.1083/jcb.201708096.
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Neuronal polarity relies on the selective localization of cargo to axons or dendrites. The molecular motor kinesin-1 moves cargo into axons but is also active in dendrites. This raises the question of how kinesin-1 activity is regulated to maintain the compartment-specific localization of cargo. Our in vivo structure–function analysis of endogenous Drosophila melanogaster kinesin-1 reveals a novel role for autoinhibition in enabling the dendrite-specific localization of Golgi outposts. Mutations that disrupt kinesin-1 autoinhibition result in the axonal mislocalization of Golgi outposts. Autoinhibition also regulates kinesin-1 localization. Uninhibited kinesin-1 accumulates in axons and is depleted from dendrites, correlating with the change in outpost distribution and dendrite growth defects. Genetic interaction tests show that a balance of kinesin-1 inhibition and dynein activity is necessary to localize Golgi outposts to dendrites and keep them from entering axons. Our data indicate that kinesin-1 activity is precisely regulated by autoinhibition to achieve the selective localization of dendritic cargo.
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Xiao, J. Z., and H. W. Kui. "Solidification of undercooled molten Cu30Ni70." Journal of Materials Research 14, no. 5 (May 1999): 1771–81. http://dx.doi.org/10.1557/jmr.1999.0239.
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Recently, it was demonstrated that grain refinement in undercooled Cu30Ni70 is brought about by a remelting of those initially formed dendrites (termed novel dendrites) which are unstable against melting. Also, it was found that in the same transition regime, there is a sharp drop in the specific volume of the undercooled specimens. Before entering into the transition regime, the novel dendrites found in an undercooled specimen are arranged in a regular pattern and the microstructures consist of large dendrites. Voids are found mainly at the dendritic spacings of the large dendrites. On the other hand, near the upper end of the transition regime, the microstructures consist of equiaxed refined grains. Furthermore, each of these grains contains a novel dendrite. Voids have moved to the interdendritic or grain boundaries. Based on these observations, a solidification mechanism of undercooled molten Cu30Ni70 is proposed.
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Dong, Yan Bo, Ming Chen, and Xi Wang. "Numerical Simulation of Binary Alloy Crystal Growth Using Phase-Field Method." Advanced Materials Research 842 (November 2013): 57–60. http://dx.doi.org/10.4028/www.scientific.net/amr.842.57.
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The competitive growth of multiple dendrites and crystal growth of directional solidification in a Mg-Al binary alloy were simulated using phase-field model, and the effect of undercooling value on the microstructural dendritic growth pattern in directional solidification process was studied in the paper. The simulation results showed the impingement of the adjacent grains, which made the dendrite growth inhibited in the competitive growth of multiple dendrites, and in directional solidification process, quantitative comparison of different undercooling values that predicted the columnar dendrite evolution were carried out. With the increasing of the undercooling value, the dendrite tip radius and second dendrite arms became smaller, and the crystal structure is more uniform and dense.
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Ozbey, Tugba, and Mehmet Bayirli. "A Numerical Study for the Relationship between Natural Manganese Dendrites and DLA Patterns." Zeitschrift für Naturforschung A 71, no. 3 (March 1, 2016): 225–34. http://dx.doi.org/10.1515/zna-2015-0406.
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AbstractThe formation mechanisms and the origin of manganese dendrites on the magnesite ore have been under discussion. The growth process of the manganese dendrites is statistically studied by comparing them to aggregations obtained according to the diffusion limited aggregation (DLA) model via Monte Carlo simulations. In this case, ten manganese dendrite patterns changing from the least dense to the densest aggregations on the surface are separately selected to determine the relationship between real and simulated patterns. The sticking parameter is ranged from 0.05≤t≤1. The density–density correlation functions C(r) (their critical exponent A), fractal dimension Df, critical exponent α, and critical exponent β pertaining to the root mean square (rms) thickness have been computed for both the ten manganese dendrites and the simulated aggregations representing them. The results indicate that manganese dendrites may be determined with the general DLA model. Analyses of manganese dendrites, both scaling and simulations, suggest the growth mechanism for the macroscopic expression of crystalline anisotropy for the dendritic patterns. These results are in good agreement with the values in other literature and can be helpful in comparing natural and simulated aggregations (both dendritic and compact deposits).
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Meunier, Claude, and Boris Lamotte d'Incamps. "Extending Cable Theory to Heterogeneous Dendrites." Neural Computation 20, no. 7 (July 2008): 1732–75. http://dx.doi.org/10.1162/neco.2008.12-06-425.
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Dendrites may exhibit many types of electrical and morphological heterogeneities at the scale of a few micrometers. Models of neurons, even so-called detailed models, rarely consider such heterogeneities. Small-scale fluctuations in the membrane conductances and the diameter of dendrites are generally disregarded and spines merely incorporated into the dendritic shaft. Using the two-scales method known as homogenization, we establish explicit expressions for the small-scale fluctuations of the membrane voltage, and we derive the cable equation satisfied by the voltage when these fluctuations are averaged out. This allows us to rigorously establish under what conditions a heterogeneous dendrite can be approximated by a homogeneous cable. We consider different distributions of synapses, orderly or random, on a passive dendrite, and we investigate when replacing excitatory and inhibitory synaptic conductances by their local averages leads to a small error in the voltage. This indicates in which regimes the approximations made in compartmental models are justified. We extend these results to active membranes endowed with voltage-dependent conductances or NMDA receptors. Then we examine under which conditions a spiny dendrite behaves as a smooth dendrite. We discover a new regime where this holds true, namely, when the conductance of the spine neck is small compared to the conductance of the synapses impinging on the spine head. Spines can then be taken into account by an effective excitatory current, the capacitance of the dendrite remaining unchanged. In this regime, the synaptic current transmitted from a spine to the dendritic shaft is strongly attenuated by the weak coupling conductance, but the total current they deliver can be quite substantial. These results suggest that pedunculated spines and stubby spines might play complementary roles in synaptic integration. Finally, we analyze how varicosities affect voltage diffusion in dendrites and discuss their impact on the spatiotemporal integration of synaptic input.
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Volfovsky, N., H. Parnas, M. Segal, and E. Korkotian. "Geometry of Dendritic Spines Affects Calcium Dynamics in Hippocampal Neurons: Theory and Experiments." Journal of Neurophysiology 82, no. 1 (July 1, 1999): 450–62. http://dx.doi.org/10.1152/jn.1999.82.1.450.
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The role of dendritic spine morphology in the regulation of the spatiotemporal distribution of free intracellular calcium concentration ([Ca2+]i) was examined in a unique axial-symmetrical model that focuses on spine–dendrite interactions, and the simulations of the model were compared with the behavior of real dendritic spines in cultured hippocampal neurons. A set of nonlinear differential equations describes the behavior of a spherical dendritic spine head, linked to a dendrite via a cylindrical spine neck. Mechanisms for handling of calcium (including internal stores, buffers, and efflux pathways) are placed in both the dendrites and spines. In response to a calcium surge, the magnitude and time course of the response in both the spine and the parent dendrite vary as a function of the length of the spine neck such that a short neck increases the magnitude of the response in the dendrite and speeds up the recovery in the spine head. The generality of the model, originally constructed for a case of release of calcium from stores, was tested in simulations of fast calcium influx through membrane channels and verified the impact of spine neck on calcium dynamics. Spatiotemporal distributions of [Ca2+]i, measured in individual dendritic spines of cultured hippocampal neurons injected with Calcium Green-1, were monitored with a confocal laser scanning microscope. Line scans of spines and dendrites at a <1-ms time resolution reveal simultaneous transient rises in [Ca2+]i in spines and their parent dendrites after application of caffeine or during spontaneous calcium transients associated with synaptic or action potential discharges. The magnitude of responses in the individual compartments, spine–dendrite disparity, and the temporal distribution of [Ca2+]i were different for spines with short and long necks, with the latter being more independent of the dendrite, in agreement with prediction of the model.
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Ferrer, I. "Dementia of Frontal Lobe Type and Amyotrophy." Behavioural Neurology 5, no. 2 (1992): 87–96. http://dx.doi.org/10.1155/1992/535897.
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Dementia of frontal lobe type may precede motor signs in a number of adult patients with amyotrophy. Neuropathological studies have shown neuron loss, spongiosis and gliosis mainly in layers II and III of the frontal and temporal lobes, together with myelin pallor of the subcortical white matter. Golgi studies revealed loss of dendritic spines on the apical dendrite of layer III pyramidal neurons, decreased numbers of dendrites, amputation and tortuosities of dendrites, and distal and proximal dendritic swellings and enlargements. Calbindin D-28K immunocytochemistry revealed a marked decrease in the number of cortical immunoreactive neurons and loss of immunoreactivity in dendrites of the remaining cells. These features indicate that pyramidal and non-pyramidal neurons in layers II and III are severely damaged, and suggest that cortical processing is seriously impaired in patients with frontal lobe type dementia.
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Roberts, Carson B., Rebecca E. Campbell, Allan E. Herbison, and Kelly J. Suter. "Dendritic Action Potential Initiation in Hypothalamic Gonadotropin-Releasing Hormone Neurons." Endocrinology 149, no. 7 (April 10, 2008): 3355–60. http://dx.doi.org/10.1210/en.2008-0152.
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It is dogma that action potentials are initiated at the soma/axon hillock of neurons. However, dendrites often exhibit conductances necessary for spike generation and represent functionally independent processing compartments within neurons. GnRH neurons provide an interesting neuronal phenotype with simple, relatively unbranched, unipolar or bipolar dendrites of extensive lengths (>1000 μm) covered in spines. These neurons control fertility and must integrate a variety of internal homeostatic and external environmental cues. We used imaging, electrophysiological, and modeling studies to understand how they integrate and process information along dendrites. Simultaneous recordings from distal dendrites and somata of individual GnRH neurons indicate distal dendrites are the primary site of spike initiation in these cells. Compartmental modeling indicates that sites of spike initiation depend upon location of excitatory input and dendrite geometry. Together, these studies demonstrate a novel pattern of spike generation in mammalian neurons and indicate that afferent inputs within distal dendritic microdomains directly initiate action potentials.
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Schoen, Alan, Ali Salehiomran, Matthew E. Larkum, and Erik P. Cook. "A Compartmental Model of Linear Resonance and Signal Transfer in Dendrites." Neural Computation 24, no. 12 (December 2012): 3126–44. http://dx.doi.org/10.1162/neco_a_00366.
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Dendrites carry signals between synapses and the soma and play a central role in neural computation. Although they contain many nonlinear ion channels, their signal-transfer properties are linear under some experimental conditions. In experiments with continuous-time inputs, a resonant linear two-port model has been shown to provide a near-perfect fit to the dendrite-to-soma input-output relationship. In this study, we focused on this linear aspect of signal transfer using impedance functions that replace biophysical channel models in order to describe the electrical properties of the dendritic membrane. The membrane impedance model of dendrites preserves the accuracy of the two-port model with minimal computational complexity. Using this approach, we demonstrate two membrane impedance profiles of dendrites that reproduced the experimentally observed two-port results. These impedance profiles demonstrate that the two-port results are compatible with different computational schemes. In addition, our model highlights how dendritic resonance can minimize the location-dependent attenuation of signals at the resonant frequency. Thus, in this model, dendrites function as linear-resonant filters that carry signals between nonlinear computational units.
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Gramatikov, Dimitar, and Svetomir Hadzi Jordanov. "Extraordinary regularities of zinc dendrites’ growth under appropriate electrolysis conditions." Journal of the Serbian Chemical Society, no. 00 (2022): 29. http://dx.doi.org/10.2298/jsc220122029g.
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A case study is given of dendritic growth during zinc electrolysis in conditions that promote it. Subject of the main interest was how the electrolysis parameters affect the duration of dendrites life. The selected set of parameters did provide a surprisingly regular dendrite?s life, i.e. period from start of the electrolysis until dendrites detachment from the cathode. Dendrite?s growth did proceed with lowering of the zinc current efficiency, and the end of life was manifested by intensive hydrogen evolution due to corrosion of detached zinc deposit in the acid electrolyte. Current efficiency was successfully followed by the bubble counting technique, invented especially for kinetic studies of gas including reactions. The acquired results on dendrites? life duration were so exact that it was easy to unify all five mono-variable dependencies into one five-variable expression. The calculated values of life duration did differ from the measured ones by only ?3%! This is a proof that the developed expression accurately presents the real nature of dendritic growth under the applied conditions, i.e. 0.5 to 2 M zinc (II) ions, 0.41 to 3.06 M H2SO4, 10 to 2500 mg dm-3 copper (II) ions, 0.14 to 14 g dm-3 hexamethylenetetramine, and 4.25 to 103 mA dm-2 current density. The eventual broader region of Zn dendrites? strict regular growth is not excluded.
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Galenko, Peter K., Dieter M. Herlach, G. Phanikumar, and O. Funke. "Phase-Field Modeling of Dendritic Solidification in Undercooled Droplets Processed by Electromagnetic Levitation." Materials Science Forum 508 (March 2006): 431–36. http://dx.doi.org/10.4028/www.scientific.net/msf.508.431.
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The results on modeling dendritic solidification from undercooled melts processed by the electromagnetic levitation technique are discussed. In order to model the details of formation of dendritic patterns we use a phase-field model of dendritic growth in a pure undercooled system with convection of the liquid phase. The predictions of the phase-field model are discussed referring to our latest high accuracy measurements of dendrite growth velocities in nickel samples. Special emphasis is given to the growth of dendrites at small and moderate undercoolings. At small undercoolings, the theoretical predictions deviate systematically from experimental data for solidification of nickel dendrites. It is shown that small amounts of impurities and forced convective flow can lead to an enhancement of the velocity of dendritic solidification at small undercoolings.
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Wan, Weihao, Dongling Li, Haizhou Wang, Lei Zhao, Xuejing Shen, Dandan Sun, Jingyang Chen, and Chengbo Xiao. "Automatic Identification and Quantitative Characterization of Primary Dendrite Microstructure Based on Machine Learning." Crystals 11, no. 9 (September 2, 2021): 1060. http://dx.doi.org/10.3390/cryst11091060.
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Dendrites are important microstructures in single-crystal superalloys. The distribution of dendrites is closely related to the heat treatment process and mechanical properties of single-crystal superalloys. The primary dendrite arm spacing (PDAS) is an important length scale to describe the distribution of dendrites. In this work, the second-generation single crystal superalloy HT901 with a diameter of 15 mm was imaged under a metallurgical microscope. An automatic dendrite core identification and full-field quantitative statistical analysis method is proposed to automatically detect the dendrite core and calculate the local PDAS. The Faster R-CNN algorithm combined with test time augmentation (TTA) technology is used to automatically identify the dendrite cores. The local multi-directional algorithm combined with Voronoi tessellation is used to determine the local nearest neighbor dendrite and calculate the local PDAS and coordination number. The accuracy of using Faster R-CNN combined with TTA to detect the dendrite core of HT901 reaches 98.4%, which is 15.9% higher than using Faster R-CNN alone. The algorithm calculates the local PDAS of all dendrites in H901 and captures the Gaussian distribution of the local PDAS. The average PDAS determined by the Gaussian distribution is 415 μm, which is only a small difference from the average spacing λ¯ (420 μm) calculated by the traditional method. The technology analyzes the relationship between the local PDAS and the distance from the center of the sample. The local PDAS near the center of HT901 are larger than those near the edge. The results suggests that the method enables the rapid, accurate and quantitative dendritic distribution characterization.
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Nosov Yu. G., Krymov V. M., Vasiliev M.G., . Chikiryaka A.V., and Nikolaev V..i. "Formation of a dendrite structure in crystals NiFeGaCo alloy in the process of growing by the Stepanov method." Physics of the Solid State 64, no. 14 (2022): 2430. http://dx.doi.org/10.21883/pss.2022.14.54345.167.
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The process of growing crystals of the NiFeGaCo alloy by the Stepanov method has been developed. It was found that the structural perfection is disturbed by the formation of dendrites, which are distributed inhomogeneously both along the length and in the cross sections of the crystals. The blocking effect of the dendrites on growth crystals of the martensite phase, which appears when the samples are cooled to the temperature of the transition of the crystal to the martensite state, is found. The elemental composition of dendritic formations was studied and it was shown that the iron content in the dendrite is approximately 30% higher, and the gallium content is 40% lower than in the matrix. Based on the modeling of heat transfer processes in the real growth zone, taking into account the experiments performed, recommendations were obtained for suppressing the formation of dendrites Keywords: Dendritic structure, shape memory alloys, Stepanov's method.
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Gao, Zihao, Changsheng Zhu, Meiling Qi, Canglong Wang, Yinlong Wang, and Borui Zhao. "Multi-phase field model simulation based on MPI+OpenMP parallel: Evolution of seaweed and dendritic structure in directional solidification." AIP Advances 12, no. 3 (March 1, 2022): 035018. http://dx.doi.org/10.1063/5.0084012.
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A multi-phase model was established to imitate the growth of algal and dendritic grains during directional solidification. We studied the effects of temperature on the growth of bi-crystals and quantitatively analyzed the influence of anisotropic strength, thermal gradient, and pulling velocity on the evolution of bi-crystals. The results show that both weaker anisotropy strength and smaller pulling velocity can maintain the formation of seaweed tissue. The increase in the pulling velocity can degenerate the seaweed grains into dendrites and improve the growth rate of the dendrites, which make grain B produce more spindles, thereby accelerating the elimination of grain A. The thermal gradient is inversely proportional to the average initial spacing of dendrites. When the thermal gradient is too small, dendritic dendrites produce developed secondary dendrite arms, which, in turn, develop into tertiary dendrite arms to occupy the grain boundary, accelerating the elimination of seaweed grains. In addition, the multi-phase field model is solved by using central processing unit serial computation, single MPI (message passing interface) parallel programming method calculation, and MPI+OpenMP hybrid parallel programming structure, and the relevant factors affecting the efficiency of program operation are analyzed and tested. By comparing the computational efficiency of the three methods, it can be seen that the MPI+OpenMP hybrid parallel programming technology can make full use of computing resources in the case of large computing scale, further optimize the MPI parallel model, and obtain a higher acceleration ratio.
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Liu, Huan, Wei Dong Xuan, Xing Fu Ren, Bao Jun Wang, Jian Bo Yu, and Zhong Ming Ren. "Effect of a High Magnetic Field on the Microstructure of Directionally Solidified NiAl-Cr(Mo)-Si Near-Eutectic Alloy at Different Withdrawal Rates." Materials Science Forum 898 (June 2017): 407–12. http://dx.doi.org/10.4028/www.scientific.net/msf.898.407.
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The effect of a 6T high magnetic field on the microstructure of directionally solidified NiAl-Cr (Mo)-Si near-eutectic alloy was investigated at the withdrawal rates of 2, 10 and 50 μm/s. The results showed that the microstructure evolved from planar eutectic to primary NiAl dendrites + cellular eutectic and then to dendritic eutectic with the increasing withdrawal rate. When the magnetic field was imposed, the well-aligned eutectic lamellae were disturbed and transformed into a wavy one at 2 μm/s. When the withdrawal rate increased to 10 μm/s, the application of the magnetic field destroyed the primary NiAl dendrite array and caused the occurrence of columnar-to-equiaxed transition (CET) of the NiAl dendrites. The volume fraction of primary dendrites also decreased. In addition, the width of intercellular/interdendritic regions decreased in cellular/dendritic eutectic structures when directionally solidified under the magnetic field. The above results should be attributed to the combined action of the thermoelectric magnetic force and the thermoelectric magnetic convection.
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Liang, Fengyi. "Sustentacular Cell Enwrapment of Olfactory Receptor Neuronal Dendrites: An Update." Genes 11, no. 5 (April 30, 2020): 493. http://dx.doi.org/10.3390/genes11050493.
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The pseudostratified olfactory epithelium (OE) may histologically appear relatively simple, but the cytological relations among its cell types, especially those between olfactory receptor neurons (ORNs) and olfactory sustentacular cells (OSCs), prove more complex and variable than previously believed. Adding to the complexity is the short lifespan, persistent neurogenesis, and continuous rewiring of the ORNs. Contrary to the common belief that ORN dendrites are mostly positioned between OSCs, recent findings indicate a sustentacular cell enwrapped configuration for a majority of mature ORN dendrites at the superficial layer of the OE. After vertically sprouting out from the borderlines between OSCs, most of the immature ORN dendrites undergo a process of sideways migration and terminal maturation to become completely invaginated into and enwrapped by OSCs. Trailing the course of the dendritic sideways migration is the mesodendrite (mesentery of the enwrapped dendrite) made of closely apposed, cell junction connected plasma membrane layers of neighboring folds of the host sustentacular cell. Only a minority of the mature ORN dendrites at the OE apical surface are found at the borderlines between OSCs (unwrapped). Below I give a brief update on the cytoarchitectonic relations between the ORNs and OSCs of the OE. Emphasis is placed on the enwrapment of ORN dendrites by OSCs, on the sideways migration of immature ORN dendrites after emerging from the OE surface, and on the terminal maturation of the ORNs. Functional implications of ORN dendrite enwrapment and a comparison with myelination or Remak’s bundling of axons or axodendrites in the central and peripheral nervous system are also discussed.
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Oakley, J. C., P. C. Schwindt, and W. E. Crill. "Dendritic Calcium Spikes in Layer 5 Pyramidal Neurons Amplify and Limit Transmission of Ligand-Gated Dendritic Current to Soma." Journal of Neurophysiology 86, no. 1 (July 1, 2001): 514–27. http://dx.doi.org/10.1152/jn.2001.86.1.514.
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Long-lasting, dendritic, Ca2+-dependent action potentials (plateaus) were investigated in layer 5 pyramidal neurons from rat neocortical slices visualized by infrared-differential interference contrast microscopy to understand the role of dendritic Ca2+ spikes in the integration of synaptic input. Focal glutamate iontophoresis on visualized dendrites caused soma firing rate to increase linearly with iontophoretic current until dendritic Ca2+ responses caused a jump in firing rate. Increases in iontophoretic current caused no further increase in somatic firing rate. This limitation of firing rate resulted from the inability of increased glutamate to change evoked plateau amplitude. Similar nonlinear patterns of soma firing were evoked by focal iontophoresis on the distal apical, oblique, and basal dendrites, whereas iontophoresis on the soma and proximal apical dendrite only evoked a linear increase in firing rate as a function of iontophoretic current without plateaus. Plateau amplitude recorded in the soma decreased as the site of iontophoresis was moved farther from the soma, consistent with decremental propagation of the plateau to the soma. Currents arriving at the soma summed if plateaus were evoked on separate dendrites or if subthreshold responses were evoked from sites on the same dendrite. If plateaus were evoked at two sites on the same dendrite, only the proximal plateau was seen at the soma. Just-subthreshold depolarizations at two sites on the same dendrite could sum to evoke a plateau at the proximal site. We conclude that the plateaus prevent current from ligand-gated channels distal to the plateau-generating region from reaching the soma and directly influencing firing rate. The implications of plateau properties for synaptic integration are discussed.
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Wang, Wenli, Wenqiang Liu, Xin Yang, Rongrong Xu, and Qiuyun Dai. "Multi-scale simulation of the dendrite growth during selective laser melting of rare earth magnesium alloy." Modelling and Simulation in Materials Science and Engineering 30, no. 1 (December 9, 2021): 015005. http://dx.doi.org/10.1088/1361-651x/ac3ca3.
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Abstract The solidification microstructure of the alloy fabricated by the selective-laser-melting (SLM) process can significantly impact its mechanical properties. In this study, a multi-scale model which couples the macroscale model for thermal-fluid and microscale cellular automata (CA) was proposed to simulate the complex solidification evolution and the dendrite growth (from planar to cellular to dendritic growth) during the SLM process. The solid–liquid interface of CA was dispersed with the bilinear interpolation method. On that basis, the curvature was accurately determined, and the calculation result was well verified by employing the Kurz–Giovanola–Trivedi analytical solution. The dendrite morphology, solute distribution, and primary dendrite arm spacing during the solidification of the SLM molten pool were quantitatively analyzed with the proposed model, well consistent with the experiment. The distribution of the undercooling field and the concentration field at the tip of dendrites different orientations were analyzed, and the two competing growth mechanisms of converging and diverging growth were revealed. Moreover, the research also indicates that during the growth of dendrites, the result of dendrite competition is determined by the height of the dendrite tip position in the direction of the thermal gradient, while the distribution of the concentration field (symmetrical or asymmetric) at the tip of the dendrite critically impacted the competing growth form of dendrites.
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van Vreeswijk, Carl, and Farzada Farkhooi. "Noise-induced properties of active dendrites." Proceedings of the National Academy of Sciences 118, no. 34 (August 19, 2021): e2023381118. http://dx.doi.org/10.1073/pnas.2023381118.
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Dendrites play an essential role in the integration of highly fluctuating input in vivo into neurons across all nervous systems. Yet, they are often studied under conditions where inputs to dendrites are sparse. The dynamic properties of active dendrites facing in vivo–like fluctuating input thus remain elusive. In this paper, we uncover dynamics in a canonical model of a dendritic compartment with active calcium channels, receiving in vivo–like fluctuating input. In a single-compartment model of the active dendrite with fast calcium activation, we show noise-induced nonmonotonic behavior in the relationship of the membrane potential output, and mean input emerges. In contrast, noise can induce bistability in the input–output relation in the system with slowly activating calcium channels. Both phenomena are absent in a noiseless condition. Furthermore, we show that timescales of the emerging stochastic bistable dynamics extend far beyond a deterministic system due to stochastic switching between the solutions. A numerical simulation of a multicompartment model neuron shows that in the presence of in vivo–like synaptic input, the bistability uncovered in our analysis persists. Our results reveal that realistic synaptic input contributes to sustained dendritic nonlinearities, and synaptic noise is a significant component of dendritic input integration.
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Kilo, Lukas, Tomke Stürner, Gaia Tavosanis, and Anna B. Ziegler. "Drosophila Dendritic Arborisation Neurons: Fantastic Actin Dynamics and Where to Find Them." Cells 10, no. 10 (October 16, 2021): 2777. http://dx.doi.org/10.3390/cells10102777.
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Neuronal dendrites receive, integrate, and process numerous inputs and therefore serve as the neuron’s “antennae”. Dendrites display extreme morphological diversity across different neuronal classes to match the neuron’s specific functional requirements. Understanding how this structural diversity is specified is therefore important for shedding light on information processing in the healthy and diseased nervous system. Popular models for in vivo studies of dendrite differentiation are the four classes of dendritic arborization (c1da–c4da) neurons of Drosophila larvae with their class-specific dendritic morphologies. Using da neurons, a combination of live-cell imaging and computational approaches have delivered information on the distinct phases and the time course of dendrite development from embryonic stages to the fully developed dendritic tree. With these data, we can start approaching the basic logic behind differential dendrite development. A major role in the definition of neuron-type specific morphologies is played by dynamic actin-rich processes and the regulation of their properties. This review presents the differences in the growth programs leading to morphologically different dendritic trees, with a focus on the key role of actin modulatory proteins. In addition, we summarize requirements and technological progress towards the visualization and manipulation of such actin regulators in vivo.
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Zhao, Shan-Rong, Hai-Jun Xu, Rong Liu, Qin-Yan Wang, and Xian-Yu Liu. "Twin and topotactic growth of β-eucryptite dendrites and their lattice coincidence analysed by the reticular theory." Journal of Applied Crystallography 46, no. 1 (January 17, 2013): 216–23. http://dx.doi.org/10.1107/s0021889812047553.
Full textAbstract:
Snowflake-shaped dendrites of β-eucryptite–β-quartz solid solution were artificially crystallized in a matt glaze, and the crystallographic orientation of the dendrites was analysed by the electron backscatter diffraction (EBSD) technique. The six branches of a snowflake-shaped dendrite in the plane (0001) are along 〈110〉. From the orientation determination, a twin relationship and a topotactic relationship between dendrites were found. The twin axes are [011], [0{\overline 1}1] and [210], and the twin planes perpendicular to the twin axes are ({\overline 1}2{\overline 1}2) and (1{\overline 2}12). From the reticular theory of twinning, it was calculated that the twin indexn= 2 and the obliquity ω = 3.2877°. The studied dendrite is a twin by reticular pseudomerohedry with low twin index and obliquity. In the topotactic growth, no twin elements have been found, but the three main crystallographic directions 〈001〉, 〈210〉 and 〈110〉 of the two dendritic crystals overlap each other. The degree of lattice coincidence between the two crystals in this topotactic growth is also discussed.
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Tsau, Chun-Huei, and Meng-Chi Tsai. "The Effects of Mo and Nb on the Microstructures and Properties of CrFeCoNi(Nb,Mo) Alloys." Entropy 20, no. 9 (August 29, 2018): 648. http://dx.doi.org/10.3390/e20090648.
Full textAbstract:
The effects of niobium and molybdenum additions on the microstructures, hardness and corrosion behaviors of CrFeCoNi(Nb,Mo) alloys were investigated. All of the CrFeCoNi(Nb,Mo) alloys displayed dendritic microstructures. The dendrites of CrFeCoNiNb and CrFeCoNiNb0.5Mo0.5 alloys were a hexagonal close packing (HCP) phase and the interdendrites were a eutectic structure of HCP and face-centered cubic (FCC) phases. Additionally, the dendrites of CrFeCoNiMo alloys were a simple cubic (SC) phase and the interdendrites were a eutectic structure of SC and FCC phases. The volume fraction of dendrites and interdendrites in these alloys were calculated. The influences of the volume fraction of dendrite in the alloys on the overall hardness were also discussed. The CrFeCoNiNb alloy had the larger volume fraction of dendrite and thus had the highest hardness among these alloys. The CrFeCoNi(Nb,Mo) alloys also showed better corrosion resistances in 1 M H2SO4 and 1 M NaCl solutions by comparing with commercial 304 stainless steel. The CrFeCoNiNb0.5Mo0.5 alloy possessed the best corrosion resistances in these solutions among the CrFeCoNi(Nb,Mo) alloys.
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Segal, M. "Fast imaging of [Ca]i reveals presence of voltage-gated calcium channels in dendritic spines of cultured hippocampal neurons." Journal of Neurophysiology 74, no. 1 (July 1, 1995): 484–88. http://dx.doi.org/10.1152/jn.1995.74.1.484.
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1. Cultured hippocampal neurons were recorded with a patch pipette containing 100 microM of the calcium indicator Fluo-3, and one of their dendrites, carrying dendritic spines, was visualized with a x100, 1.3-numerical aperture oil objective. Calcium spikes evoked by depolarizing the somata and changes in free dendrite and spine calcium concentrations ([Ca]d and [Ca]s, respectively) were monitored with a cooled charge-coupled device (CCD) camera, acquiring images at a rate of 17-20 ms per frame. In the majority of spine-dendrite pairs, [Ca]s rose faster and to a higher level than the adjacent [Ca]d. Likewise, topical application of glutamate evoked a faster and larger change in [Ca]s than in [Ca]d. The rise of intracellular calcium concentration in response to a depolarizing current pulse, but not in response to glutamate, was reduced in the presence of the calcium antagonist verapamil in both dendrites and spines. It is suggested that dendritic spines possess voltage-gated calcium channels.
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McIntyre, Alexa B. R., and Thomas A. Cleland. "Biophysical constraints on lateral inhibition in the olfactory bulb." Journal of Neurophysiology 115, no. 6 (June 1, 2016): 2937–49. http://dx.doi.org/10.1152/jn.00671.2015.
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The mitral cells (MCs) of the mammalian olfactory bulb (OB) constitute one of two populations of principal neurons (along with middle/deep tufted cells) that integrate afferent olfactory information with top-down inputs and intrinsic learning and deliver output to downstream olfactory areas. MC activity is regulated in part by inhibition from granule cells, which form reciprocal synapses with MCs along the extents of their lateral dendrites. However, with MC lateral dendrites reaching over 1.5 mm in length in rats, the roles of distal inhibitory synapses pose a quandary. Here, we systematically vary the properties of a MC model to assess the capacity of inhibitory synaptic inputs on lateral dendrites to influence afferent information flow through MCs. Simulations using passivized models with varying dendritic morphologies and synaptic properties demonstrated that, even with unrealistically favorable parameters, passive propagation fails to convey effective inhibitory signals to the soma from distal sources. Additional simulations using an active model exhibiting action potentials, subthreshold oscillations, and a dendritic morphology closely matched to experimental values further confirmed that distal synaptic inputs along the lateral dendrite could not exert physiologically relevant effects on MC spike timing at the soma. Larger synaptic conductances representative of multiple simultaneous inputs were not sufficient to compensate for the decline in signal with distance. Reciprocal synapses on distal MC lateral dendrites may instead serve to maintain a common fast oscillatory clock across the OB by delaying spike propagation within the lateral dendrites themselves.
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Frick, A., W. Zieglgänsberger, and H. U. Dodt. "Glutamate Receptors Form Hot Spots on Apical Dendrites of Neocortical Pyramidal Neurons." Journal of Neurophysiology 86, no. 3 (September 1, 2001): 1412–21. http://dx.doi.org/10.1152/jn.2001.86.3.1412.
Full textAbstract:
Apical dendrites of layer V cortical pyramidal neurons are a major target for glutamatergic synaptic inputs from cortical and subcortical brain regions. Because innervation from these regions is somewhat laminar along the dendrites, knowing the distribution of glutamate receptors on the apical dendrites is of prime importance for understanding the function of neural circuits in the neocortex. To examine this issue, we used infrared-guided laser stimulation combined with whole cell recordings to quantify the spatial distribution of glutamate receptors along the apical dendrites of layer V pyramidal neurons. Focally applied (<10 μm) flash photolysis of caged glutamate on the soma and along the apical dendrite revealed a highly nonuniform distribution of glutamate responsivity. Up to four membrane areas (extent 22 μm) of enhanced glutamate responsivity (hot spots) were detected on the dendrites with the amplitude and integral of glutamate-evoked responses at hot spots being three times larger than responses evoked at neighboring sites. We found no association of these physiological hot spots with dendritic branch points. It appeared that the larger responses evoked at hot spots resulted from an increase in activation of both α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) and N-methyl-d-aspartate (NMDA) receptors and not a recruitment of voltage-activated sodium or calcium conductances. Stimulation of hot spots did, however, facilitate the triggering of both Na+ spikes and Ca2+ spikes, suggesting that hot spots may serve as dendritic initiation zones for regenerative spikes.
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Kloosterman, Fabian, Pascal Peloquin, and L. Stan Leung. "Apical and Basal Orthodromic Population Spikes in Hippocampal CA1 In Vivo Show Different Origins and Patterns of Propagation." Journal of Neurophysiology 86, no. 5 (November 1, 2001): 2435–44. http://dx.doi.org/10.1152/jn.2001.86.5.2435.
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There is controversy concerning whether orthodromic action potentials originate from the apical or basal dendrites of CA1 pyramidal cells in vivo. The participation of the dendrites in the initialization and propagation of population spikes in CA1 of urethan-anesthetized rats in vivo was studied using simultaneously recorded field potentials and current source density (CSD) analysis. CSD analysis revealed that the antidromic population spike, evoked by stimulation of the alveus, invaded in succession, the axon initial segment (stratum oriens), cell body and ∼200 μm of the proximal apical dendrites. Excitation of the basal dendrites of CA1, following stimulation of CA3 stratum oriens, evoked an orthodromic spike that started near the cell body or initial segment and then propagated ∼200 μm into the proximal apical dendrites. In contrast, the population spike that followed excitation of the apical dendrites of CA1 initiated at the proximal apical dendrites, 50–100 μm distal to the cell body layer, and then propagated centripetally to the cell body and the proximal basal dendrites. A late apical dendritic spike may arise in the mid-apical dendrites (250–300 μm from the cell layer) and propagated distally. The origin or the pattern of propagation of each population spike type was similar for near-threshold to supramaximal stimulus intensities. In summary, population spikes following apical dendritic and basal dendritic excitation in vivo appeared to originate from different locations. Apical dendritic excitation evoked a population spike that initiated in the proximal apical dendrites while basal dendritic excitation evoked a spike that started near the initial segment or cell body. An original finding of this study is the propagation of the population spike from basal to apical dendrites in vivo or vice versa. This backpropagation from one dendritic tree to the other may play an important role in the synaptic plasticity among a network of CA3 to CA1 neurons.
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Hundekar, Prateek, Swastik Basu, Xiulin Fan, Lu Li, Anthony Yoshimura, Tushar Gupta, Varun Sarbada, et al. "In situ healing of dendrites in a potassium metal battery." Proceedings of the National Academy of Sciences 117, no. 11 (March 2, 2020): 5588–94. http://dx.doi.org/10.1073/pnas.1915470117.
Full textAbstract:
The use of potassium (K) metal anodes could result in high-performance K-ion batteries that offer a sustainable and low-cost alternative to lithium (Li)-ion technology. However, formation of dendrites on such K-metal surfaces is inevitable, which prevents their utilization. Here, we report that K dendrites can be healed in situ in a K-metal battery. The healing is triggered by current-controlled, self-heating at the electrolyte/dendrite interface, which causes migration of surface atoms away from the dendrite tips, thereby smoothening the dendritic surface. We discover that this process is strikingly more efficient for K as compared to Li metal. We show that the reason for this is the far greater mobility of surface atoms in K relative to Li metal, which enables dendrite healing to take place at an order-of-magnitude lower current density. We demonstrate that the K-metal anode can be coupled with a potassium cobalt oxide cathode to achieve dendrite healing in a practical full-cell device.
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Al-Gahtani, Masoud, and Rian Dippenaar. "Mechanical Properties of Dendritic and Inter-Dendritic Regions in As-Cast Medium-Carbon Steel." Advanced Materials Research 894 (February 2014): 104–9. http://dx.doi.org/10.4028/www.scientific.net/amr.894.104.
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During solidification of steel, dendrite nucleation and growth leads to the segregation of alloying elements in the inter-dendritic regions. The dendrite arms are low in carbon while alloying elements segregate to the inter-dendritic regions. During subsequent hot-rolling, this variation in alloying element content leads to the formation of regions of high and low solute content, which in turn, leads to the formation of microstructural banding during heat treatment. In the present study, the respective mechanical properties of these dendritic and inter-dendritic regions were studied in medium carbon steel in order to investigate the rotation of dendrites during hot rolling.
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Lowe, Graeme. "Inhibition of Backpropagating Action Potentials in Mitral Cell Secondary Dendrites." Journal of Neurophysiology 88, no. 1 (July 1, 2002): 64–85. http://dx.doi.org/10.1152/jn.2002.88.1.64.
Full textAbstract:
The mammalian olfactory bulb is a geometrically organized signal-processing array that utilizes lateral inhibitory circuits to transform spatially patterned inputs. A major part of the lateral circuitry consists of extensively radiating secondary dendrites of mitral cells. These dendrites are bidirectional cables: they convey granule cell inhibitory input to the mitral soma, and they conduct backpropagating action potentials that trigger glutamate release at dendrodendritic synapses. This study examined how mitral cell firing is affected by inhibitory inputs at different distances along the secondary dendrite and what happens to backpropagating action potentials when they encounter inhibition. These are key questions for understanding the range and spatial dependence of lateral signaling between mitral cells. Backpropagating action potentials were monitored in vitro by simultaneous somatic and dendritic whole cell recording from individual mitral cells in rat olfactory bulb slices, and inhibition was applied focally to dendrites by laser flash photolysis of caged GABA (2.5-μm spot). Photolysis was calibrated to activate conductances similar in magnitude to GABAA-mediated inhibition from granule cell spines. Under somatic voltage-clamp with CsCl dialysis, uncaging GABA onto the soma, axon initial segment, primary and secondary dendrites evoked bicuculline-sensitive currents (up to −1.4 nA at −60 mV; reversal at ∼0 mV). The currents exhibited a patchy distribution along the axon and dendrites. In current-clamp recordings, repetitive firing driven by somatic current injection was blocked by uncaging GABA on the secondary dendrite ∼140 μm from the soma, and the blocking distance decreased with increasing current. In the secondary dendrites, backpropagated action potentials were measured 93–152 μm from the soma, where they were attenuated by a factor of 0.75 ± 0.07 (mean ± SD) and slightly broadened (1.19 ± 0.10), independent of activity (35–107 Hz). Uncaging GABA on the distal dendrite had little effect on somatic spikes but attenuated backpropagating action potentials by a factor of 0.68 ± 0.15 (0.45–0.60 μJ flash with 1-mM caged GABA); attenuation was localized to a zone of width 16.3 ± 4.2 μm around the point of GABA release. These results reveal the contrasting actions of inhibition at different locations along the dendrite: proximal inhibition blocks firing by shunting somatic current, whereas distal inhibition can impose spatial patterns of dendrodendritic transmission by locally attenuating backpropagating action potentials. The secondary dendrites are designed with a high safety factor for backpropagation, to facilitate reliable transmission of the outgoing spike-coded data stream, in parallel with the integration of inhibitory inputs.
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Xie, Xiao Hua, Quan Zhou, Cheng Bo Xiao, and Xin Tang. "Effect of Low-Voltage Pulsed Magnetic Field on Solidified Structure of Superalloy K4169." Applied Mechanics and Materials 423-426 (September 2013): 725–29. http://dx.doi.org/10.4028/www.scientific.net/amm.423-426.725.
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Effects of different pulse voltage and frequency on solidified structure of superalloy K4169 under low-voltage pulsed magnetic field (LVPMF) were investigated in this paper, and the related mechanism was also discussed. The experimental results show that grain of superalloy K4169 can be refined greatly by LVPMF treatment during the course of solidification. Growth of dendrite is restrained and primary grain is changed from large dendrites to smaller equiaxed grains. When the pulse voltage is at 0-280V, grain size of the alloy decreases as pulse voltage increases, and primary dendrites are fractured from well-developed dendrites into fine equiaxed grains and non-dendritic structures. When the pulse frequency is at 0-5Hz, the increase of pulse frequency enhances the refinement effect of LVPMF processing. With the increase of the pulse frequency, grain size of the alloy increases.