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dc.creatorCabeza, Jose M.es
dc.creatorAcosta López, Jorgees
dc.creatorAlés González de la Higuera, Eva Maríaes
dc.date.accessioned2021-08-23T10:41:17Z
dc.date.available2021-08-23T10:41:17Z
dc.date.issued2013-05-24
dc.identifier.citationCabeza, J.M., Acosta López, J. y Alés González de la Higuera, E.M. (2013). Mechanisms of Granule Membrane Recapture followingExocytosis in Intact Mast Cells. Journal of Biological Chemistry, 288 (28), 20293-20305.
dc.identifier.issn0021-9258 (impreso)es
dc.identifier.issn1083-351X (electrónico)es
dc.identifier.urihttps://hdl.handle.net/11441/125142
dc.description.abstractIn secretory cells, several exocytosis-coupled forms of endocytosis have been proposed including clathrin-mediated endocytosis, kiss-and-run endocytosis, cavicapture, and bulk endocytosis. These forms of endocytosis can be induced under different conditions, but their detailed molecular mechanisms and functions are largely unknown. We studied exocytosis and endocytosis in mast cells with both perforated-patch and whole-cell configurations of the patch clamp technique using cell capacitance measurements in combination with amperometric serotonin detection. We found that intact mast cells exhibit an early endocytosis that follows exocytosis induced by compound 48/80. Direct observation of individual exocytic and endocytic events showed a higher percentage of capacitance flickers (27.3%) and off-steps (11.4%) in intact mast cells than in dialyzed cells (5.4% and 2.9%, respectively). Moreover, we observed a type of endocytosis of large pieces of membrane that were likely formed by cumulative fusion of several secretory granules with the cell membrane. We also identified “large-capacitance flickers” that occur after large endocytosis events. Pore conductance analysis indicated that these transient events may represent “compound cavicapture,” most likely due to the flickering of a dilated fusion pore. Using fluorescence imaging of individual exocytic and endocytic events we observed that granules can fuse to granules already fused with the plasma membrane, and then the membranes and dense cores of fused granules are internalized. Altogether, our results suggest that stimulated exocytosis in intact mast cells is followed by several forms of compensatory endocytosis, including kiss-and-run endocytosis and a mechanism for efficient retrieval of the compound membrane of several secretory granules through a single membrane fission event. Background: When vesicles undergo exocytosis, the vesicle membrane must be retrieved by endocytosis to maintain a constant cell surface area. Results: Exocytosis in intact mast cells is followed by endocytosis. Conclusion: Mechanisms of granule membrane recapture in intact mast cells include kiss-and-run and “compound endocytosis.” Significance: Compound endocytosis may be a novel mechanism for efficiently compensating for the membrane excess caused by exocytosis.es
dc.description.sponsorshipMinisterio de Ciencia e Innovación ISCIIIand Fondos FEDER Grant PI11/00257es
dc.formatapplication/pdfes
dc.format.extent13 p.es
dc.language.isoenges
dc.publisherAmerican Society for Biochemistry and Molecular Biologyes
dc.relation.ispartofJournal of Biological Chemistry, 288 (28), 20293-20305.
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectEndocytosises
dc.subjectExocytosises
dc.subjectMast Celles
dc.subjectMembrane Fusiones
dc.subjectVesicleses
dc.subjectAmperometryes
dc.subjectCapacitancees
dc.subjectCavicapturees
dc.subjectFusion Porees
dc.subjectKiss-and-runes
dc.titleMechanisms of Granule Membrane Recapture followingExocytosis in Intact Mast Cellses
dc.typeinfo:eu-repo/semantics/articlees
dcterms.identifierhttps://ror.org/03yxnpp24
dc.type.versioninfo:eu-repo/semantics/publishedVersiones
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.contributor.affiliationUniversidad de Sevilla. Departamento de Fisiología Médica y Biofísicaes
dc.relation.projectIDGrant PI11/00257es
dc.identifier.doi10.1074/jbc.M113.459065es
dc.journaltitleJournal of Biological Chemistryes
dc.publication.volumen288es
dc.publication.issue28es
dc.publication.initialPage20293es
dc.publication.endPage20305es

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