Transient fusion ensures granule replenishment to enable repeated release after IgE-mediated mast cell degranulation

To ensure normal immune function, mast cells employ different pathways to release mediators. Here, we report a thus far unknown capacity of mast cells to recycle and reuse secretory granules after an antigen-evoked degranulation process under physiological conditions; this phenomenon involves the ex...

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Veröffentlicht in:Journal of cell science 2016-11, Vol.129 (21), p.3989-4000
Hauptverfasser: Balseiro-Gomez, Santiago, Flores, Juan A, Acosta, Jorge, Ramirez-Ponce, M Pilar, Ales, Eva
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container_end_page 4000
container_issue 21
container_start_page 3989
container_title Journal of cell science
container_volume 129
creator Balseiro-Gomez, Santiago
Flores, Juan A
Acosta, Jorge
Ramirez-Ponce, M Pilar
Ales, Eva
description To ensure normal immune function, mast cells employ different pathways to release mediators. Here, we report a thus far unknown capacity of mast cells to recycle and reuse secretory granules after an antigen-evoked degranulation process under physiological conditions; this phenomenon involves the existence of a recycling secretory granule pool that is available for release in a short time scale. Rapid endocytic modes contributed to the recycling of ∼60% of the total secretory granule population, which involved kiss-and-run and cavicapture mechanisms, causing retention of the intragranular matrix. We found the presence of normal-size granules and giant actomyosin- and dynamin-dependent granules, which were characterized by large quantal content. These large structures allowed the recovered mast cells to release a large amount of 5-HT, compensating for the decrease in the number of exocytosed secretory granules. This work uncovers a new physiological role of the exo-endocytosis cycle in the immunological plasticity of mast cells and reveals a new property of their biological secretion.
doi_str_mv 10.1242/jcs.194340
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source MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection; Company of Biologists
subjects Actins - metabolism
Animals
Antigens - metabolism
Calcimycin - pharmacology
Cell Degranulation - drug effects
Dynamins - metabolism
Electrochemical Techniques
Endocytosis - drug effects
Exocytosis - drug effects
Immunoglobulin E - metabolism
Mast Cells - drug effects
Mast Cells - physiology
Membrane Fusion - drug effects
Mice, Inbred C57BL
Models, Biological
Myosin Type II - metabolism
Secretory Vesicles - drug effects
Secretory Vesicles - metabolism
Serotonin - metabolism
title Transient fusion ensures granule replenishment to enable repeated release after IgE-mediated mast cell degranulation
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