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Littérature scientifique sur le sujet « Endosomal trafficking »

Auteur : Grafiati

Publié le 4 juin 2021

Mis à jour le 9 février 2022

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Articles de revues sur le sujet "Endosomal trafficking"

Lee, Samuel M., Lih-Shen Chin, and Lian Li. "Charcot-Marie-Tooth disease-linked protein SIMPLE functions with the ESCRT machinery in endosomal trafficking." Journal of Cell Biology 199, no. 5 (2012): 799–816. http://dx.doi.org/10.1083/jcb.201204137.

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Mutations in small integral membrane protein of lysosome/late endosome (SIMPLE) cause autosomal dominant, Charcot-Marie-Tooth disease (CMT) type 1C. The cellular function of SIMPLE is unknown and the pathogenic mechanism of SIMPLE mutations remains elusive. Here, we report that SIMPLE interacted and colocalized with endosomal sorting complex required for transport (ESCRT) components STAM1, Hrs, and TSG101 on early endosomes and functioned with the ESCRT machinery in the control of endosome-to-lysosome trafficking. Our analyses revealed that SIMPLE was required for efficient recruitment of ESCR

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Tzafriri, A. Rami, and Elazer R. Edelman. "Endosomal receptor kinetics determine the stability of intracellular growth factor signalling complexes." Biochemical Journal 402, no. 3 (2007): 537–49. http://dx.doi.org/10.1042/bj20060756.

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There is an emerging paradigm that growth factor signalling continues in the endosome and that cell response to a growth factor is defined by the integration of cell surface and endosomal events. As activated receptors in the endosome are exposed to a different set of binding partners, they probably elicit differential signals compared with when they are at the cell surface. As such, complete appreciation of growth factor signalling requires understanding of growth factor–receptor binding and trafficking kinetics both at the cell surface and in endosomes. Growth factor binding to surface recep

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Aikawa, Yoshikatsu, Kara L. Lynch, Kristin L. Boswell, and Thomas F. J. Martin. "A Second SNARE Role for Exocytic SNAP25 in Endosome Fusion." Molecular Biology of the Cell 17, no. 5 (2006): 2113–24. http://dx.doi.org/10.1091/mbc.e06-01-0074.

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Soluble N-ethylmaleimide-sensitive factor attachment protein receptor (SNARE) proteins play key roles in membrane fusion, but their sorting to specific membranes is poorly understood. Moreover, individual SNARE proteins can function in multiple membrane fusion events dependent upon their trafficking itinerary. Synaptosome-associated protein of 25 kDa (SNAP25) is a plasma membrane Q (containing glutamate)-SNARE essential for Ca2+-dependent secretory vesicle–plasma membrane fusion in neuroendocrine cells. However, a substantial intracellular pool of SNAP25 is maintained by endocytosis. To assess

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Shideler, Tess, Daniel P. Nickerson, Alexey J. Merz, and Greg Odorizzi. "Ubiquitin binding by the CUE domain promotes endosomal localization of the Rab5 GEF Vps9." Molecular Biology of the Cell 26, no. 7 (2015): 1345–56. http://dx.doi.org/10.1091/mbc.e14-06-1156.

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Vps9 and Muk1 are guanine nucleotide exchange factors (GEFs) in Saccharomyces cerevisiae that regulate membrane trafficking in the endolysosomal pathway by activating Rab5 GTPases. We show that Vps9 is the primary Rab5 GEF required for biogenesis of late endosomal multivesicular bodies (MVBs). However, only Vps9 (but not Muk1) is required for the formation of aberrant class E compartments that arise upon dysfunction of endosomal sorting complexes required for transport (ESCRTs). ESCRT dysfunction causes ubiquitinated transmembrane proteins to accumulate at endosomes, and we demonstrate that en

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Witte, Leonie, Karen Linnemannstöns, Kevin Schmidt, et al. "The kinesin motor Klp98A mediates apical to basal Wg transport." Development 147, no. 15 (2020): dev186833. http://dx.doi.org/10.1242/dev.186833.

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ABSTRACTDevelopment and tissue homeostasis rely on the tight regulation of morphogen secretion. In the Drosophila wing imaginal disc epithelium, Wg secretion for long-range signal transduction occurs after apical Wg entry into the endosomal system, followed by secretory endosomal transport. Although Wg release appears to occur from the apical and basal cell sides, its exact post-endocytic fate and the functional relevance of polarized endosomal Wg trafficking are poorly understood. Here, we identify the kinesin-3 family member Klp98A as the master regulator of intracellular Wg transport after

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Gallon, Matthew, and Peter J. Cullen. "Retromer and sorting nexins in endosomal sorting." Biochemical Society Transactions 43, no. 1 (2015): 33–47. http://dx.doi.org/10.1042/bst20140290.

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The evolutionarily conserved endosomal retromer complex rescues transmembrane proteins from the lysosomal degradative pathway and facilitates their recycling to other cellular compartments. Retromer functions in conjunction with numerous associated proteins, including select members of the sorting nexin (SNX) family. In the present article, we review the molecular architecture and cellular roles of retromer and its various functional partners. The endosomal network is a crucial hub in the trafficking of proteins through the cellular endomembrane system. Transmembrane proteins, here termed carg

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Liu, Kai, Ruxiao Xing, Youli Jian, et al. "WDR91 is a Rab7 effector required for neuronal development." Journal of Cell Biology 216, no. 10 (2017): 3307–21. http://dx.doi.org/10.1083/jcb.201705151.

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Early-to-late endosome conversion, which is essential for delivery of endosomal cargoes to lysosomes, requires switching of early endosome–specific Rab5 and PtdIns3P to late endosome–specific Rab7 and PtdIns(3,5)P2. In this study, we identify the WD40-repeat protein WDR91 as a Rab7 effector that couples Rab switching with PtdIns3P down-regulation on endosomes. Loss of WDR91 greatly increases endosomal PtdIns3P levels, arresting endosomes at an intermediate stage and blocking endosomal–lysosomal trafficking. WDR91 is recruited to endosomes by interacting with active guanosine triphosophate–Rab7

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Chotard, Laëtitia, Ashwini K. Mishra, Marc-André Sylvain, Simon Tuck, David G. Lambright, and Christian E. Rocheleau. "TBC-2 Regulates RAB-5/RAB-7-mediated Endosomal Trafficking inCaenorhabditis elegans." Molecular Biology of the Cell 21, no. 13 (2010): 2285–96. http://dx.doi.org/10.1091/mbc.e09-11-0947.

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During endosome maturation the early endosomal Rab5 GTPase is replaced with the late endosomal Rab7 GTPase. It has been proposed that active Rab5 can recruit and activate Rab7, which in turn could inactivate and remove Rab5. However, many of the Rab5 and Rab7 regulators that mediate endosome maturation are not known. Here, we identify Caenorhabditis elegans TBC-2, a conserved putative Rab GTPase-activating protein (GAP), as a regulator of endosome to lysosome trafficking in several tissues. We show that tbc-2 mutant animals accumulate enormous RAB-7–positive late endosomes in the intestine con

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Bennett, Elizabeth M., Sharron X. Lin, Mhairi C. Towler, Frederick R. Maxfield, and Frances M. Brodsky. "Clathrin Hub Expression Affects Early Endosome Distribution with Minimal Impact on Receptor Sorting and Recycling." Molecular Biology of the Cell 12, no. 9 (2001): 2790–99. http://dx.doi.org/10.1091/mbc.12.9.2790.

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Clathrin-coated vesicles execute receptor-mediated endocytosis at the plasma membrane. However, a role for clathrin in later endocytic trafficking processes, such as receptor sorting and recycling or maintaining the organization of the endocytic pathway, has not been thoroughly characterized. The existence of clathrin-coated buds on endosomes suggests that clathrin might mediate later endocytic trafficking events. To investigate the function of clathrin-coated buds on endosomal membranes, endosome function and distribution were analyzed in a HeLa cell line that expresses the dominant-negative

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Dukes, Joseph D., Judith D. Richardson, Ruth Simmons, and Paul Whitley. "A dominant-negative ESCRT-III protein perturbs cytokinesis and trafficking to lysosomes." Biochemical Journal 411, no. 2 (2008): 233–39. http://dx.doi.org/10.1042/bj20071296.

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In eukaryotic cells, the completion of cytokinesis is dependent on membrane trafficking events to deliver membrane to the site of abscission. Golgi and recycling endosomal-derived proteins are required for the terminal stages of cytokinesis. Recently, protein subunits of the ESCRT (endosomal sorting complexes required for transport) that are normally involved in late endosome to lysosome trafficking have also been implicated in abscission. Here, we report that a subunit, CHMP3 (charged multivesicular body protein-3), of ESCRT-III localizes at the midbody. Deletion of the C-terminal autoinhibit

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Thèses sur le sujet "Endosomal trafficking"

Dawson, Jonathan Edward. "Dynamics of endosomal trafficking." Doctoral thesis, Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2012. http://nbn-resolving.de/urn:nbn:de:bsz:14-qucosa-90216.

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Endosomes are dynamic vesicular structures which transport cargo molecules internalized into the cell via endocytosis. Endosomal trafficking of cargo involves a large number of individual endosomes that regularly interact with each other via fusion and fission and thus form a dynamic network wherein endocytosed cargo is sorted and transported to various other intracellular compartments. In this study we present a general theoretical framework that takes into account individual endosomes and several key microscopic interaction processes among them. By combining theory with quantitative experime

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Struthers, Marion Symington. "An evolutionarily conserved regulatory mechanism for endosomal membrane trafficking." Thesis, University of Glasgow, 2009. http://theses.gla.ac.uk/1350/.

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Membrane fusion in all eukaryotic cells is facilitated by the formation of SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein receptor) complexes; a process that is regulated by Sec1p/Munc18 (SM) proteins. Membrane fusion has been conserved through evolution and hence a lot or our knowledge about the molecular mechanism that regulates membrane traffic has come from experimentally tractable model organisms such as Saccharomyces cerevisiae. The work presented in this thesis demonstrates that the mammalian SNARE protein, syntaxin 16 (Sx16), is a functional homologue of the yeast

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Gravert, Maike. "Novel regulators of trafficking in the yeast Golgi-endosomal system." Doctoral thesis, Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2006. http://nbn-resolving.de/urn:nbn:de:swb:14-1160402018221-35061.

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Over the past few years a large amount of work has provided growing insight into the molecular mechanisms that direct post-Golgi trafficking events in the budding yeast Saccharomyces cerevisae. However, a key event in this process, the formation of secretory vesicles at the Golgi and sorting of cargo into these transport carriers, remains poorly understood. It has been demonstrated that phosphatidylinositol 4-phosphate (PI(4)P) generated by the PI(4)-kinase Pik1p plays an essential role in maintenance of Golgi secretory function and morphology. Up to now relatively few targets of Pik1/PI(4)P s

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Baumann, Adrian. "Analysis of the molecular function of kazrin in endosomal trafficking." Doctoral thesis, Universitat de Barcelona, 2018. http://hdl.handle.net/10803/664079.

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Endocytosis and endosomal trafficking are of central meaning in all eukaryotic cells. It enables cells to rapidly modify their surface exposure of signalling complexes, nutrient and ion transporters, to maintain the homeostasis of lipids and proteins, to distribute internalized material within the cell, and to initiate and maintain cell motility, among others. Hence, the endocytic uptake and transport processes can regulate the capacity of the cell to sample and react to with their environment. This thesis focused on the study of kazrin C, a human protein originally identified in our group,

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Dukes, Joseph Donaldson. "Investigating the link between phosphoinositides, endosomal trafficking and ESCRT function." Thesis, University of Bath, 2008. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.512257.

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The maturation of early endosomes into multivesicular bodies (MVBs) and subsequent trafficking to lysosomes is an important event for the control and silencing of endocytosed membrane receptors. The endosomal-sorting complex required for transport (ESCRT) proteins appear to play a key role in this event. Phosphatidylinositol lipids including PtdIns(3,5)P2 have been implicated in the MVB-lysosomal pathway and an ESCRT-III component CHMP3 binds to this lipid in vitro. The purpose of this thesis was to investigate the link between ESCRT proteins, PtdIns(3,5)P2 and endo-lysosomal trafficking. Firs

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Vistein, Rachel. "Hierarchical Sorting And Trafficking Of β - 2 Adrenergic Receptors Via Endosomal Microdomains". Research Showcase @ CMU, 2014. http://repository.cmu.edu/dissertations/370.

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A defining feature of the eukaryotic cell is the abundance and diversity of membranous organelles. This allowed for a single cell to compartmentalize various functions and laid a foundation for the specialization of cell types in multicellular organisms. Greater complexity, however, requires more work to maintain, thus cells evolved machinery for directing the trafficking of proteins to their designated membranes. Early studies on membrane trafficking focused on understanding the biosynthetic pathway that takes proteins from their initial synthesis to be excreted or inserted in the plasma memb

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Dalton, Lauren. "Using large-scale screens to identify novel regulators of endosomal trafficking in yeast." Thesis, University of British Columbia, 2016. http://hdl.handle.net/2429/60209.

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The full abstract for this thesis is available in the body of the thesis, and will be available when the embargo expires.<br>Medicine, Faculty of<br>Biochemistry and Molecular Biology, Department of<br>Graduate

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Dahan, Sophie. "Intracellular proteinmembrane trafficking : evaluation of the Golgi and endosomal apparatus by cryoimmune electron microscopy." Thesis, McGill University, 1995. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=29387.

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Protein trafficking events in the secretory and endosomal apparatus were evaluated in rat liver hepatocytes by EM immunogold cytochemistry. The cellular distribution of apolipoprotein E and other abundant hepatic secretory and endosomal proteins was quantitatively examined in ultrathin cryosections of liver hepatocytes. Under steady-state conditions, apoE was concentrated within the Golgi apparatus, along sinusoidal plasma membrane microvilli and within all components of the endosomal apparatus, as evaluated immunocytochemically and confirmed by quantitative immunoblotting of organelles isolat

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Hunt, Piper Reid. "Evidence for a maturation model of endosomal trafficking derived from analysis of human fibroblasts." Available to US Hopkins community, 2002. http://wwwlib.umi.com/dissertations/dlnow/3068170.

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Castro, Cruz Monica del Carmen. "The impact of the syndecan-PDZ interactome on endosomal trafficking and extracellular vesicle composition." Thesis, Aix-Marseille, 2018. http://www.theses.fr/2018AIXM0302.

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Les syndécans forment une famille de quatre protéines transmembranaires qui sont substituées par l'héparane sulfate. Grâce à ces chaînes glucidiques extracellulaires, les syndécans contrôlent la signalisation d'une pléthore de facteurs de croissance et de molécules d'adhésion. Une autre caractéristique remarquable des syndécans est la conservation de leur domaine intracellulaire au cours de l'évolution. Ce domaine contient un motif C-terminal qui peut induire une interaction avec les protéines dites «PDZ». Les interactions PDZ sont promiscues et les protéines PDZ contrôlent divers aspects de l

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Livres sur le sujet "Endosomal trafficking"

Dhani, Sonja Urmilla. An investigation of the endosomal trafficking of the ClC-2 chloride channel. 2006.

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Chapitres de livres sur le sujet "Endosomal trafficking"

Baumann, Sebastian, Norio Takeshita, Nathalie Grün, Reinhard Fischer, and Michael Feldbrügge. "Live Cell Imaging of Endosomal Trafficking in Fungi." In Membrane Trafficking. Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4939-2309-0_24.

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Rainero, Elena, Peter V. E. van den Berghe, and Jim C. Norman. "Internalisation, Endosomal Trafficking and Recycling of Integrins During Cell Migration and Cancer Invasion." In Vesicle Trafficking in Cancer. Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-6528-7_16.

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Calebiro, Davide, Amod Godbole, Sandra Lyga, and Martin J. Lohse. "Trafficking and Function of GPCRs in the Endosomal Compartment." In Methods in Molecular Biology. Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4939-1755-6_16.

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Daeden, Alicia, and Marcos Gonzalez-Gaitan. "Endosomal Trafficking During Mitosis and Notch-Dependent Asymmetric Division." In Endocytosis and Signaling. Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-96704-2_11.

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Shen, Wenjin, Juan Wei, and Caiji Gao. "Functional Analysis of Plant FYVE Proteins in Endosomal Trafficking." In Methods in Molecular Biology. Springer US, 2020. http://dx.doi.org/10.1007/978-1-0716-0767-1_8.

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Kalinowska, Kamila, and Erika Isono. "Analysis of Global Ubiquitylation and Ubiquitin-Binding Domains Involved in Endosomal Trafficking." In Methods in Molecular Biology. Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4939-1420-3_15.

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García-León, Marta, and Vicente Rubio. "Biochemical and Imaging Analysis of ALIX Function in Endosomal Trafficking of Arabidopsis Protein Cargoes." In Methods in Molecular Biology. Springer US, 2020. http://dx.doi.org/10.1007/978-1-0716-0767-1_5.

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Shimada, Tomoo, Yasuko Koumoto, and Ikuko Hara-Nishimura. "Evaluation of Defective Endosomal Trafficking to the Vacuole by Monitoring Seed Storage Proteins in Arabidopsis thaliana." In Methods in Molecular Biology. Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4939-1420-3_10.

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Pilecka, Iwona, and Marta Miaczynska. "Efficient Enhancement of Signaling Capacity: Signaling Endosomes." In Vesicle Trafficking in Cancer. Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-6528-7_7.

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Benarroch, Eduardo E. "Vesicular Trafficking." In Neuroscience for Clinicians, edited by Eduardo E. Benarroch. Oxford University Press, 2021. http://dx.doi.org/10.1093/med/9780190948894.003.0007.

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Normal cell function depends on the appropriate synthesis, maturation, sorting, and delivery of fully processed proteins and other macromolecules to specific intracellular compartments; uptake of material from the cell exterior; and regulated intracellular processing and degradation of proteins, lipids, complex carbohydrates, abnormal aggregates, and senescent organelles. These fundamental functions involve secretory, endocytic, and autophagic pathways. The secretory pathway is responsible for protein maturation, sorting, and delivery of transmembrane and secreted proteins from their site of synthesis to their final destinations. Synaptic vesicle exocytosis is a special form of secretion that allows rapid communication between neurons. The endocytic pathway starts with the internalization of material via endosomes. Endosomal content can be transported back to the cell body, recycled to cell compartments, or delivered for degradation by the lysosome. Abnormal protein aggregates or damaged organelles undergo autophagy, which involves formation of an autophagosome and degradation by the lysosome. Impaired vesicular trafficking is a fundamental mechanism in a large number of neurodegenerative disorders, including hereditary spastic paraplegia, lower motor neuron syndromes, and Parkinson disease.

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Actes de conférences sur le sujet "Endosomal trafficking"

Ferrati, Silvia, Rita E. Serda, Andrew Bean, and Mauro Ferrari. "Intracellular Trafficking of Nano-Carriers." In ASME 2010 First Global Congress on NanoEngineering for Medicine and Biology. ASMEDC, 2010. http://dx.doi.org/10.1115/nemb2010-13303.

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A multistage delivery system based on biodegradable mesoporous silicon particles loaded with one or multiple second stage nano-particles is likely to be useful for drug delivery. Upon intravenous injection the silicon nano-carriers will travel through the blood stream and migrate to the vessel wall. Vascular endothelial cells have been shown to be promising candidates for drug delivery as they represent both an anchor point and target.[1] It has been shown that human endothelial cells can act as nonprofessional phagocytes internalizing our silicon micron-sized nano-carriers.[2] The complete un

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White, Zachary B., Centdrika Dates Hurt, Rajani Rajbhandari, Sindhu Nair, Susan Nozell, and Markus Bredel. "Abstract 3758: Impact of ANXA7 I1 expression on PDGFRA and MET endosomal trafficking in glioblastoma." In Proceedings: AACR Annual Meeting 2020; April 27-28, 2020 and June 22-24, 2020; Philadelphia, PA. American Association for Cancer Research, 2020. http://dx.doi.org/10.1158/1538-7445.am2020-3758.

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Indraccolo, S., M. Pinazza, M. Ghisi, et al. "PO-114 Histone deacetylase 6 regulates NOTCH3 endosomal trafficking and degradation in T-cell acute lymphoblastic leukaemia cells." In Abstracts of the 25th Biennial Congress of the European Association for Cancer Research, Amsterdam, The Netherlands, 30 June – 3 July 2018. BMJ Publishing Group Ltd, 2018. http://dx.doi.org/10.1136/esmoopen-2018-eacr25.155.

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Lee, Sook, Sandip K. Basu, Vijay Walia, Deborah K. Morrison, and Peter F. Johnson. "Abstract A11: Oncogenic Ras signaling involves sustained perinuclear localization of the effector kinases p-ERK1/2 and CK2 via KSR-1 and endosomal trafficking." In Abstracts: AACR Special Conference on RAS Oncogenes: From Biology to Therapy; February 24-27, 2014; Lake Buena Vista, FL. American Association for Cancer Research, 2014. http://dx.doi.org/10.1158/1557-3125.rasonc14-a11.

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Basu, Sandip K., Sook Lee, Krisada Sakchaisri та ін. "Abstract A35: Oncogenic Ras signaling involves formation of perinuclear CK2α nd p-ERK1/2 signaling complexes that require the KSR-1 scaffold protein and endosomal trafficking". У Abstracts: Fourth AACR International Conference on Frontiers in Basic Cancer Research; October 23-26, 2015; Philadelphia, PA. American Association for Cancer Research, 2016. http://dx.doi.org/10.1158/1538-7445.fbcr15-a35.

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