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Relevant bibliographies by topics / Plasmalema

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Academic literature on the topic 'Plasmalema'

Author: Grafiati

Published: 4 June 2021

Last updated: 7 February 2022

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Journal articles on the topic "Plasmalema"

1

ISHIKAWA, Harunori. "Plasmalemmal undercoat: The cytoskeleton supporting the plasmalemma." Archives of Histology and Cytology 51, no. 2 (1988): 127–45. http://dx.doi.org/10.1679/aohc.51.127.

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Peters, K. R., W. W. Carley, and G. E. Palade. "Endothelial plasmalemmal vesicles have a characteristic striped bipolar surface structure." Journal of Cell Biology 101, no. 6 (December 1, 1985): 2233–38. http://dx.doi.org/10.1083/jcb.101.6.2233.

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Capillary endothelial cells have a large population of small (65-80 nm diameter in transmission electron microscopy) vesicles of which a large fraction is associated with the plasmalemma of the luminal and abluminal side. We studied the fine structure and distribution of these plasmalemmal vesicles by high resolution scanning electron microscopy in cultured endothelial cells obtained from bovine adrenal cortical capillaries. Cell monolayers were covered with polylysine-coated silicon chips, split in high potassium buffer, fixed in aldehyde mixtures, and then treated with OsO4 and thiocarbohydrazide. After critical point drying, the specimens were coated with a thin (less than 2 nm) continuous film of chromium. On the cytoplasmic aspect of the dorsal plasmalemmal fragments seen in such specimens, plasmalemmal vesicles appear as uniform vesicular protrusions approximately 70-90 nm in diameter, preferentially concentrated in distinct large fields in which they occur primarily as single units. Individual plasmalemmal vesicles exhibit a striped surface fine structure which consists of ridges approximately 10 nm in diameter, separated by furrows and oriented as meridians, often ending at two poles on opposite sides of the vesicles in a plane parallel to the plasmalemma. This striped surface structure is clearly distinct from the cage structure of coated pits found, at low surface density, on the same specimens. The cytoplasmic aspect of the plasmalemma proper is covered by a fibrillar infrastructure which does not extend over plasmalemmal vesicles but on which the latter appear to be anchored by fine filaments.

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3

Kordylewski, L., T. Karrison, and E. Page. "Measurements on the internal structure of freeze-fractured cardiac plasma membrane." American Journal of Physiology-Heart and Circulatory Physiology 248, no. 3 (March 1, 1985): H297—H304. http://dx.doi.org/10.1152/ajpheart.1985.248.3.h297.

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We describe a quantitative analysis of the internal structure of cardiac plasma membranes freeze fractured in situ, including the P-face particle density (lambda), the P-face particle diameter (d), the percent of fracture face area occupied by particles (Ap), and the spatial distribution of particles (random, clustered, or ordered). This analysis has been applied to seven sheep hearts to compare the plasmalemmal internal structures in ventricular and atrial myocytes and Purkinje strands of the same hearts and also to myocytes of frog, chicken, rabbit, and rat ventricles (to compare internal plasmalemmal structure of different vertebrate classes). Measurements were made on tissues conventionally prepared for freeze fracture by glutaraldehyde fixation and cryoprotection. We found that, in the same sheep hearts, lambda and Ap for ventricular plasmalemma significantly exceeded those for atrial plasmalemma and that the distribution of atrial P-face particles was more clustered than that for ventricle. d and Ap for frog ventricular plasmalemmal P-face significantly exceeded values for some of the other vertebrates.

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4

Façanha, Arnoldo Rocha, Anna Lvovna Okorokova Façanha, Fábio Lopes Olivares, Fernando Guridi, Gabriel de Araújo Santos, Ary Carlos Xavier Velloso, Victor Marcos Rumjanek, et al. "Bioatividade de ácidos húmicos: efeitos sobre o desenvolvimento radicular e sobre a bomba de prótons da membrana plasmática." Pesquisa Agropecuária Brasileira 37, no. 9 (September 2002): 1301–10. http://dx.doi.org/10.1590/s0100-204x2002000900014.

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A bioatividade de ácidos húmicos (AH) isolados de lodo da estação de tratamento de esgoto (AHL) e de vermicomposto (AHV) foi avaliada pela ação dessas substâncias sobre o transporte de prótons através da membrana plasmática de células de raízes de café e milho e sua relação com o desenvolvimento dessas espécies. Houve estímulo da área superficial radicular em ambas as espécies cultivadas com ambos AH, mostrando uma concentração ótima em torno de 40 mg L-1. Nessa condição, os tratamentos com AHL e AHV estimularam a H+-ATPase de membrana plasmática em plântulas de café e milho. Os AHL foram mais efetivos na promoção desses efeitos do que os AHV. A modificação do perfil cromatográfico dos AH em solução antes e após o cultivo das plântulas revelou que a interação planta-AH promoveu uma redistribuição das massas moleculares dessas substâncias, sugerindo uma dinâmica de mobilização de subunidades funcionais dos AH por exsudatos das raízes. A análise estrutural dos AH detectou a presença de grupamentos de auxina. A análise comparativa da ação desses dois AH sobre as espécies representantes de plantas monocotiledôneas (milho) e dicotiledôneas (café) apontam para a ativação da H+-ATPase de plasmalema como possível marcador metabólico de bioatividade dos ácidos húmicos.

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5

Muresan, V., and M. C. Constantinescu. "Distribution of sialoglycoconjugates on the luminal surface of the endothelial cell in the fenestrated capillaries of the pancreas." Journal of Histochemistry & Cytochemistry 33, no. 5 (May 1985): 474–76. http://dx.doi.org/10.1177/33.5.3989274.

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Sialic acid-bearing molecules on the luminal surface of the vascular endothelium in mouse and rat pancreatic capillaries were detected electron microscopically by using a procedure with ferritin hydrazide (FH), after preferential oxidation of sialyl residues with sodium periodate. The distribution of FH on the endothelial surface demonstrated the existence of microdomains with various densities of sialoglycoconjugates oxidizable by sodium periodate and accessible to the tracer. On the plasmalemma proper, FH binding sites were heterogeneously distributed. Their concentration on various microdomains decreased as follows: plasmalemma proper greater than coated pits greater than stomal diaphragms of plasmalemmal vesicles and transendothelial channels, and fenestral diaphragms. The membrane of plasmalemmal vesicles and transendothelial channels was not labeled by FH. Nonspecific binding of FH to the nonoxidized endothelial surface or that oxidized after neuraminidase treatment was relatively low.

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6

Predescu, D., M. Simionescu, N. Simionescu, and G. E. Palade. "Binding and transcytosis of glycoalbumin by the microvascular endothelium of the murine myocardium: evidence that glycoalbumin behaves as a bifunctional ligand." Journal of Cell Biology 107, no. 5 (November 1, 1988): 1729–38. http://dx.doi.org/10.1083/jcb.107.5.1729.

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The binding and transport of glycoalbumin (gA) by the endothelium of murine myocardial microvessels were studied by perfusing in situ 125I-gA or gA-gold complexes (gA-Au) and examining the specimens by radioassays and EM, respectively. After a 3-min perfusion, the uptake of radioiodinated gA is 2.2-fold higher than that of native albumin; it is partially (approximately 55%) competed by either albumin or D-glucose, and almost completely abolished by the concomitant administration of both competitors or by gA. D-mannose and D-galactose are not effective competitors. Unlike albumin-gold complexes that bind restrictively to plasmalemmal vesicles, gA-Au labels the plasma-lemma proper, plasmalemmal vesicles open on the lumen, and most coated pits. Competing albumin prevents gA-Au binding to the membrane of plasmalemmal vesicles, while glucose significantly reduces the ligand binding to plasmalemma proper. Competition with albumin and glucose gives additive effects. Transcytosis of gA-Au, already detected at 3 min, becomes substantial by 30 min. No tracer exit via intercellular junctions was detected. gA-Au progressively accumulates in multivesicular bodies. The results of the binding and competition experiments indicate that the gA behaves as a bifunctional ligand which is recognized by two distinct binding sites: one, located on the plasma membrane, binds as a lectin the glucose residues of gA; whereas the other, confined to plasmalemmal vesicles, recognizes presumably specific domains of the albumin molecule.

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Stan, R. V., W. G. Roberts, D. Predescu, K. Ihida, L. Saucan, L. Ghitescu, and G. E. Palade. "Immunoisolation and partial characterization of endothelial plasmalemmal vesicles (caveolae)." Molecular Biology of the Cell 8, no. 4 (April 1997): 595–605. http://dx.doi.org/10.1091/mbc.8.4.595.

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Plasmalemmal vesicles (PVs) or caveolae are plasma membrane invaginations and associated vesicles of regular size and shape found in most mammalian cell types. They are particularly numerous in the continuous endothelium of certain microvascular beds (e.g., heart, lung, and muscles) in which they have been identified as transcytotic vesicular carriers. Their chemistry and function have been extensively studied in the last years by various means, including several attempts to isolate them by cell fractionation from different cell types. The methods so far used rely on nonspecific physical parameters of the caveolae and their membrane (e.g., size-specific gravity and solubility in detergents) which do not rule out contamination from other membrane sources, especially the plasmalemma proper. We report here a different method for the isolation of PVs from plasmalemmal fragments obtained by a silica-coating procedure from the rat lung vasculature. The method includes sonication and flotation of a mixed vesicle fraction, as the first step, followed by specific immunoisolation of PVs on anticaveolin-coated magnetic microspheres, as the second step. The mixed vesicle fraction, is thereby resolved into a bound subfraction (B), which consists primarily of PVs or caveolae, and a nonbound subfraction (NB) enriched in vesicles derived from the plasmalemma proper. The results so far obtained indicate that some specific endothelial membrane proteins (e.g., thrombomodulin, functional thrombin receptor) are distributed about evenly between the B and NB subfractions, whereas others are restricted to the NB subfraction (e.g., angiotensin converting enzyme, podocalyxin). Glycoproteins distribute unevenly between the two subfractions and antigens involved in signal transduction [e.g., annexin II, protein kinase C alpha, the G alpha subunits of heterotrimeric G proteins (alpha s, alpha q, alpha i2, alpha i3), small GTP-binding proteins, endothelial nitric oxide synthase, and nonreceptor protein kinase c-src] are concentrated in the NB (plasmalemma proper-enriched) subfraction rather than in the caveolae of the B subfraction. Additional work should show whether discrepancies between our findings and those already recorded in the literature represent inadequate fractionation techniques or are accounted for by chemical differentiation of caveolae from one cell type to another.

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Williams, JB. "Studies on the Epidermis of Temnocephala Vii.* The Basal Region, with Comments on 'Membrane Flow'." Australian Journal of Zoology 33, no. 4 (1985): 413. http://dx.doi.org/10.1071/zo9850413.

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Tubular infoldings of the plasmalemma, and other basal structures in the epidermis of Temnocephala novaezealandiae, are described. At times, the tubular invaginations are greatly elaborated, resulting in a considerably increased plasmalemmal area; also, complex lateral interdigitations occur at the boundaries of the differentiated syncytial epithelia. Many mitochondria are associated with the elaborated membrane. These modifications suggest an enhanced ion transport across the epidermis, and the epidermis is assumed to function in combination with the protonephridial tubules in ionic regulation. Other cytoplasmic structures are correlated with the enhanced plasma membrane, indicating possible pathways of membraneogenesis. Return to the normal epidermal cytomorphology evidently entails a large-scale disassembly of plasma membranes.

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9

Roettger, B. F., R. U. Rentsch, D. Pinon, E. Holicky, E. Hadac, J. M. Larkin, and L. J. Miller. "Dual pathways of internalization of the cholecystokinin receptor." Journal of Cell Biology 128, no. 6 (March 15, 1995): 1029–41. http://dx.doi.org/10.1083/jcb.128.6.1029.

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Receptor molecules play a major role in the desensitization of agonist-stimulated cellular responses. For G protein-coupled receptors, rapid desensitization occurs via receptor phosphorylation, sequestration, and internalization, yet the cellular compartments in which these events occur and their interrelationships are unclear. In this work, we focus on the cholecystokinin (CCK) receptor, which has been well characterized with respect to phosphorylation. We have used novel fluorescent and electron-dense CCK receptor ligands and an antibody to probe receptor localization in a CCK receptor-bearing CHO cell line. In the unstimulated state, receptors were diffusely distributed over the plasmalemma. Agonist occupation stimulated endocytosis via both clathrin-dependent and independent pathways. The former was predominant, leading to endosomal and lysosomal compartments, as well as recycling to the plasmalemma. The clathrin-independent processes led to a smooth vesicular compartment adjacent to the plasmalemma resembling caveolae, which did not transport ligand deeper within the cell. Potassium depletion largely eliminated clathrin-dependent endocytosis, while not interfering with agonist-stimulated receptor movement into subplasmalemmal smooth vesicle compartments. These cellular endocytic events can be related to the established cycle of CCK receptor phosphorylation and dephosphorylation, which we have previously described (Klueppelberg, U. G., L. K. Gates, F. S. Gorelick, and L. J. Miller. 1991. J. Biol. Chem. 266:2403-2408; Lutz, M. P., D. I. Pinon, L. K. Gates, S. Shenolikar, and L. J. Miller. 1993. J. Biol. Chem. 268:12136-12142). The rapid onset and peak of receptor phosphorylation after agonist occupation correlates best with a plasmalemmal localization, while stimulated receptor phosphatase activity correlates best with receptor residence in intracellular compartments. We postulate that the smooth vesicular compartment adjacent to the plasmalemma functions for the rapid resensitization of the receptor, while the classical clathrin-mediated endocytotic pathway is key for receptor downregulation via lysosomal degradation, as well as less rapid resensitization.

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Simionescu, M., N. Simionescu, F. Santoro, and G. E. Palade. "Differentiated microdomains of the luminal plasmalemma of murine muscle capillaries: segmental variations in young and old animals." Journal of Cell Biology 100, no. 5 (May 1, 1985): 1396–407. http://dx.doi.org/10.1083/jcb.100.5.1396.

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We investigated the luminal surface of the continuous endothelium of the microvasculature of the murine heart and diaphragm to find out whether it has differentiated microdomains. The probes were ferritin molecules, cationized to pI's 6.8, 7.15, 7.6, 8.0 and 8.4, which were introduced by retrograde or anterograde perfusion through the aorta or vena cava after the blood was removed from the vasculature. The pattern of labeling was analyzed by electron microscopy and assessed quantitatively by morphometry in arterioles, capillaries, and venules identified in bipolar microvascular fields in the diaphragm. The results showed that the plasmalemma proper was heavily but discontinuously labeled by all cationized ferritins (CF) used, the labeling being less extensive on the venular endothelium. CF had access as individual molecules to a fraction of the vesicular population opened on the luminal front of the endothelium. Plasmalemmal vesicle labeling increased from approximately 10 to approximately 25% as the pI decreased from 8.4 to 6.8. Vesicle labeling also increased with CF concentration in the perfusate. All CF binding sites were removed by pronase and papain. Heparinase and heparitinase caused only a slight reduction in CF labeling. Neuraminidase decreased the extent and density of labeling, especially on the plasmalemma proper of the venular endothelium; this decrease was particularly pronounced in old animals.

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Dissertations / Theses on the topic "Plasmalema"

1

Norman, P. M. "Plant plasmalemma structure : An immunological approach." Thesis, Open University, 1986. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.379102.

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Fordham, Michael. "The plasmalemma as the primary site of action of ozone." Thesis, University of Newcastle Upon Tyne, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.241315.

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Xuan, Guangchi. "Plasmaless automated xenon difluoride MEMS etching system development and application." Access to citation, abstract and download form provided by ProQuest Information and Learning Company; downloadable PDF file, 71 p, 2006. http://proquest.umi.com/pqdweb?did=1163250891&sid=1&Fmt=2&clientId=8331&RQT=309&VName=PQD.

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Spitta, Luis Fernando [Verfasser]. "Phosphatidylcholine is organized in long-lived plasmalemmal platforms / Luis Fernando Spitta." Bonn : Universitäts- und Landesbibliothek Bonn, 2013. http://d-nb.info/1044868929/34.

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Predescu, Sanda. "Plasmalemmal vesicles (caveolae) are special vesicular carriers involved in endothelial transcytosis /." Diss., Connect to a 24 p. preview or request complete full text in PDF format. Access restricted to UC campuses, 1999. http://wwwlib.umi.com/cr/ucsd/fullcit?p9944218.

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Blein, J. P. "Etude de l'action de quelques carbanilates sur le plasmalemme de cellules d'érable." Grenoble 2 : ANRT, 1986. http://catalogue.bnf.fr/ark:/12148/cb375960893.

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Blein, Jean-Pierre. "Étude de l'action de quelques carbanilates sur le plasmalemme de cellules d'érable." Paris 11, 1986. http://www.theses.fr/1986PA112020.

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Dans cette thèse, nous avons rapporté les caractéristiques biochimiques des ATPases associées à la membrane plasmique de cellule d’Acer pseudoplanatus. Nous avons également démontré que la membrane plasmique renferme des systèmes d’oxydo-réduction dont le fonctionnement acidifie le milieu extracellulaire. Parmi 51 carbanilates analogues d’un herbicide, le SWEP, nous avons mis en évidence 10 molécules inhibitrices des ATPases du plasmalemme de cellules végétales ou animales. Ces molécules sont sans action sur les ATPases mitochondriales et sur les phosphohydrolases solubles, et semblent donc posséder une bonne spécificité pour les ATPases tonoplastiques. D’autre part, 14 carbanilates analogues d’un autre herbicide, le phenmédiphame, se sont révélés comme des inhibiteurs des systèmes d’oxydo-réduction étudiés. Ces molécules se sont révélées toxiques pour les suspensions cellulaires utilisées, et leurs effets in vivo ont pu être expliqués par leur action biochimique déterminée in vitro. Elles n’ont pas exprimé cependant d’effets toxiques importants lorsqu’elles ont été administrées à des plantes. Nous avons ensuite apporté des arguments en faveur d’un couplage entre les systèmes d’oxydo-réduction et les ATPases associés à la membrane plasmique. Dans une telle hypothèse, les ATPases assureraient le transport des protons générés par le fonctionnement des systèmes d’oxydo-réduction. Ce couplage pourrait être indirect, par l’intermédiaire du gradient électrochimique des protons, ou direct, par l’intermédiaire d’un facteur moléculaire de couplage. En conséquence, on en arrive à la conclusion que les sites d’action des différents carbanilates étudiés pourraient être les ATPases ou/et les systèmes d’oxydo-réduction proprement dits, ou encore le ou les site(s) de couplage. Ces différentes possibilités sont discutées, et un schéma récapitulatif du mécanisme d’action des molécules étudiées est proposé
A study has been carried out to characterize the biochemical properties of plasmalemma ATPase from Acer pseudoplatanus cells, and to report evidences for the presence of a trans-plasmamembrane electron transport system, the activity of which is associated with a concomitant external medium acidification. Among 51 carbanilates derived from the herbicide SWEP, we have found 10 specific inhibitors of plasmalemma ATPases. These chemicals are inactive on the mitochondrial ATPase, and the soluble phosphatase activities (the tonoplastic enzyme was not studied). On the other hand, 14 carbanilate derivatives from another herbicide (phenmedipham) appear as inhibitors of trans-membrane redox systems. These chemicals are toxic for in vitro cell cultures, and these cytotoxic properties are consistent with their biochemical mode of action. This toxicity is not expressed at the whole plant level, however. Moreover, we report evidences for a coupling between the redox systems and the ATPases associated with plasmalemma. In this way, ATPases could perform the transport of protons provided by the activity of the redox systems. This coupling, which results in a mutual regulation of the two systems, could be governed by the electrochemical proton gradient, or by a molecular site. According to these possibilities, the target of the two groups of carbanilates could be either the ATPases or the redox systems associated with the plasmalemma, or the site of coupling. These different possibilities, which are not mutually exclusive, are discussed, and a recapitulative scheme of the mechanism of action of the inhibitors is proposed

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Mpaga-Mbadinga, Adèle. "Effets du potassium sur la Mg-ATPase du plasmalemme de cellules de racines de maïs." Grenoble 2 : ANRT, 1987. http://catalogue.bnf.fr/ark:/12148/cb37608254s.

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Bourdil, Isabelle. "Étude des activités NAD(P)H-ferricyanure oxydoréductase associées au plasmalemme des racines de mai͏̈s." Toulouse, INPT, 1990. http://www.theses.fr/1990INPT008A.

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Les activites nad(p) h-ferricyanure reductases ont ete etudiees sur du plasmalemme de racines de mais, prepare par centrifugations differentielles, sedimentation a travers un coussin de saccharose et partage de phases polymeres. Cette fraction microsomale est exempte de contaminations par d'autres membranes cellulaires et est constituee a 85-90% de vesicules membranaires fermees dans le sens natif. L'orientation des vesicules a ete determinee a partir de la mesure de la latence de l'activite atpase plasmique. L'etude des activites nad(p) h-ferricyanure reductases a permis de mettre en evidence la presence d'au moins trois activites differentes, differenciees par leurs specificites pour le nadh ou le nadph, leurs optima de ph et leurs sensibilites aux detergents et a la thermolysine. C'est ainsi qu'une activite nadh-ferricyanure reductase maximale a ph 7,0 est mesuree en absence de detergent, independante du niveau de solubilisation des membranes par les detergents et sensible a la thermolysine. Elle serait situee a la surface externe de la membrane plasmique. Une activite nadh-ferricyanure reductase maximale a ph 5,0 et une activite nadph-ferricyanure reductase maximale a ph 7,0, sont entierement revelees a la solubilisation complete des membranes par les detergents et insensibles a la thermolysine. Elles seraient situees a la surface interne de la membrane plasmique. Enfin, cette etude suggere egalement la presence d'une activite nadh-ferricyanure reductase, maximale a ph 7,0 localisee a la surface interne de la membrane plasmique. Des tentatives de purification de ces activites ont montre que deux activites nadh-ferricyanure reductases peuvent etre separees par chromatographie d'affinite en eluant a differentes concentrations en nadh

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Alves, Georges. "Les cellules associées aux vaisseaux (CAVs) chez Juglans regia : étude de l'ATPase-H+ du plasmalemme." Clermont-Ferrand 2, 2003. http://www.theses.fr/2003CLF21475.

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Chez les angiospermes, les cellules associées aux vaisseaux (CAVs) sont situées à la jonction entre les voies de transport vertical de la sève xylémienne et les voies de transport radial des nutriments. Les flux de sucres entre ces deux tissus via les CAVs se font par 2 mouvements opposés : l'efflux et l'influx. L'influx se ferait par un co-transport H+/sucres dépendant du gradient de pH généré par l'ATPase-H+ du plasmalemme. Nous avons entrepris d'étudier les CAVs et notamment leurs ATPases-H=+ du plasmalemme afin de définir leurs rôles chez le noyer. En hiver, nous avons observé, une faible activité de l'ATPase-H+ du plasmalemme dans la partie apicale du rameau, contrairement à la partie basale. Au printemps, à la reprise de croissance, nous avons observé une forte activité de l'APTase et un fort marquage dans des les VACs de la partie apicale du rameau. Ces résultats sont bien corrélés à l'évolution des capacités de débourrement des bourgeons sur un rameau de l'année

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Books on the topic "Plasmalema"

1

Towards funtional complementation cloning of the gene for the plasmalemmal carnitine transporter defect: Selective media development and initial transfections. Ottawa: National Library of Canada, 1996.

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Book chapters on the topic "Plasmalema"

1

Sussman, Michael R. "A Plethora of Plant Plasmalemma Proton Pumps." In Transport and Receptor Proteins of Plant Membranes, 5–11. Boston, MA: Springer US, 1992. http://dx.doi.org/10.1007/978-1-4615-3442-6_1.

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Lüttge, Ulrich, and David T. Clarkson. "Mineral Nutrition: Plasmalemma and Tonoplast Redox Activities." In Progress in Botany, 73–86. Berlin, Heidelberg: Springer Berlin Heidelberg, 1985. http://dx.doi.org/10.1007/978-3-642-45607-7_6.

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Ullrich-Eberius, C. I., J. Pavlovkin, J. Schindel, K. Fischer, and A. Novacky. "Changes in Plasmalemma Functions Induced by Phytopathogenic Bacteria." In Plasma Membrane Oxidoreductases in Control of Animal and Plant Growth, 323–32. Boston, MA: Springer US, 1988. http://dx.doi.org/10.1007/978-1-4684-8029-0_36.

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Hagimoto, Yoshiya, Hajime Ugajin, Daisuke Miyakoshi, Hayato Iwamoto, Yusuke Muraki, and Takehiko Orii. "Evaluation of the Plasmaless Gaseous Etching Process." In Solid State Phenomena, 7–10. Stafa: Trans Tech Publications Ltd., 2007. http://dx.doi.org/10.4028/3-908451-46-9.7.

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Cseh, E., and F. Fodor. "Role of boron in the plasmalemma turbo reductase activity." In Boron in Soils and Plants, 175–77. Dordrecht: Springer Netherlands, 1997. http://dx.doi.org/10.1007/978-94-011-5564-9_34.

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Thiel, G., and G. O. Kirst. "Ferricyanide Changes the Transport Properties of Lamprothamnium Papulosum Plasmalemma." In Plasma Membrane Oxidoreductases in Control of Animal and Plant Growth, 263–71. Boston, MA: Springer US, 1988. http://dx.doi.org/10.1007/978-1-4684-8029-0_29.

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Moreau, P., H. Juguelin, R. Lessire, and C. Cassagne. "Study of the Intracellular Transfer of Lipids to the Plasmalemma." In The Metabolism, Structure, and Function of Plant Lipids, 221–24. Boston, MA: Springer New York, 1987. http://dx.doi.org/10.1007/978-1-4684-5263-1_40.

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Schubert, S., F. Yan, H. S. Howind, and R. Feuerle. "Veränderungen der H+-ATPase-Aktivität im Plasmalemma von Maiswurzelzellen unter Säurestress." In Mikroökologische Prozesse im System Pflanze-Boden, 85–88. Wiesbaden: Vieweg+Teubner Verlag, 1995. http://dx.doi.org/10.1007/978-3-322-83428-7_17.

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Barr, R., and F. L. Crane. "Are Plasmalemma Redox Protons Involved in Growth Control by Plant Cells?" In Plasma Membrane Oxidoreductases in Control of Animal and Plant Growth, 408. Boston, MA: Springer US, 1988. http://dx.doi.org/10.1007/978-1-4684-8029-0_52.

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Sokolik, A. I., Zh Visotskaya, E. Krytynskaya, and V. Yurin. "Interaction of ion-transport mechanisms at the plasmalemma of plant cells." In Plant Nutrition, 200–201. Dordrecht: Springer Netherlands, 2001. http://dx.doi.org/10.1007/0-306-47624-x_96.

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Conference papers on the topic "Plasmalema"

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Obroucheva, N. V., S. V. Lityagina, and I. A. Sinkevich. "ROLE OF PLASMALEMMA H+-ATPASE IN SEED GERMINATION." In The All-Russian Scientific Conference with International Participation and Schools of Young Scientists "Mechanisms of resistance of plants and microorganisms to unfavorable environmental". SIPPB SB RAS, 2018. http://dx.doi.org/10.31255/978-5-94797-319-8-571-574.

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morqenstern, E., and H. Patscheke. "THE SECRETORY PATHWAY IN PLATELETS STUDIED BY CRYO-FIXATION." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643491.

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Abstract:

It is widely held, that the constituents packed in the a -granules are released by stimulated platelets via the surface connected system (SCS). By means of the fast-freezing and freeze substitution technique (which allow the investigation of membrane fusion) we found a secretory pathway in platelets (compound exocytosis) without an involvement of the SCS during the release of a-granules. To study the process of a-granule secretion human platelets concentrated in citrated blood plasm were stimulated with thrombin or collagen. 20 - 120 seconds after stimulation the platelets were rapidly frozen with a metal-mirror attachment to the KF 80 cryofixation unit (REICHERT-JUNG). Using plastic spacers droplets of the PRP were slammed against a copper block at 80 K at a rate of 0.2 m/sec. After cryofixation the specimens were transferred (in liquid nitrogen) into a Cs-auto cryosubstitution unit (REICHERT-JUNG). Cryosubstitution was programmed for 48h at 193 K in acetone with 4% osmium tetroxide. The temperature went automatically up to room temperature at a rate of 10 K/h. The specimens were embedded in araldite. The analysis of serial ultrathin sections of platelets in different phases of exocytosis revealed the following. a -granules in apposition showed different stages of swelling and dispersal of their electron dense matrix. Membrane appositions were also found between a -granules. The contraction of a sphere of microfilaments and microtubules during stimulation seemed to support this process. On the other hand this internal contraction prevented most of the a-granules from contacting with the plasmalemma. We observed fusion between swollen -granules in apposition and the plasmalemma and swollen and unswollen a -granules. Thus, large compound granules were formed frequently before fusion of the secretory organelles with the plasmalemma took place. These observations suggested that a -granules in stimulated platelets performed a compound exocytosis after swelling. The process seemed to start with the apposition of a -granule membranes to the plasmalemma. It cannot yet be answered whether the swelling of the granules is due to an osmotically driven influx of water or due to an influx after microfusion.Supported by DFG, Grant Mo 124/2-4

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Formisano, Alessandro, Andrea Gaetano Chiariello, Raffaele Martone, Shakeib Arshad, and George Vayakis. "Error Field In Tokamaks: A Plasmaless Measurements Approach." In 1st EPS conference on Plasma Diagnostics. Trieste, Italy: Sissa Medialab, 2016. http://dx.doi.org/10.22323/1.240.0101.

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Obroucheva, N. V., I. A. Sinkevich, and S. V. Lityagina. "DEEP DORMANCY RELEASE IN HORSE CHESTNUT SEEDS AND ACTIVATION OF PLASMALEMMA H+-ATPASE." In The All-Russian Scientific Conference with International Participation and Schools of Young Scientists "Mechanisms of resistance of plants and microorganisms to unfavorable environmental". SIPPB SB RAS, 2018. http://dx.doi.org/10.31255/978-5-94797-319-8-575-579.

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Zhou, Ling-Yun, Can-Bang Zhang, Sheng-Yu Wang, Lin Xu, and Gang-Min Wu. "Analysis of microscopic mechanism on electricity and thermology effects of laser-plasmalemma interaction." In SPIE Proceedings, edited by Qingming Luo, Lihong V. Wang, Valery V. Tuchin, and Min Gu. SPIE, 2007. http://dx.doi.org/10.1117/12.741368.

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Wilkinson, Alex, Daniel Patten, Sam Hulme, Matthew Hoare, and Shishir Shetty. "P029 Plasmalemma vesicle-associated protein (PLVAP) mediates monocyte transmigration across human hepatic sinusoidal endothelium in response to the senescent secretome." In Abstracts of the British Association for the Study of the Liver Annual Meeting, 22–24 November 2021. BMJ Publishing Group Ltd and British Society of Gastroenterology, 2021. http://dx.doi.org/10.1136/gutjnl-2021-basl.38.

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