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The Journal of Immunology, 1998, 161: 5120-5123.
Copyright © 1998 by The American Association of Immunologists


CUTTING EDGE

Cutting Edge: Ca2+-Dependent Exocytosis in Mast Cells Is Stimulated by the Ca2+ Sensor, Synaptotagmin I1

Dana Baram*,{dagger}, Michal Linial{ddagger}, Yoseph A. Mekori{dagger} and Ronit Sagi-Eisenberg2,*

* Department of Cell Biology and Histology, Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel; {dagger} Allergy and Clinical Immunology Unit, Sapir Medical Center, Kfar Saba, Israel; and {ddagger} Department of Biological Chemistry, Life Sciences Institute, Hebrew University in Jerusalem, Jerusalem, Israel

Mast cells secrete a variety of biologically active substances that mediate inflammatory responses. Synaptotagmin(s) (Syts) are a gene family of proteins that are implicated in the control of Ca2+-dependent exocytosis. In the present study, we investigated the possible occurrence and functional involvement of Syt in the control of mast cell exocytosis. Here, we demonstrate that both connective tissue type and mucosal-like mast cells express Syt-immunoreactive proteins, and that these proteins are localized almost exclusively to their secretory granules. Furthermore, expression of Syt I, the neuronal Ca2+ sensor, in rat basophilic leukemia cells (RBL-2H3), a tumor analogue of mucosal mast cells, resulted in prominent potentiation and acceleration of Ca2+-dependent exocytosis. Therefore, these findings implicate Syt as a Ca2+ sensor that mediates regulated secretion in mast cells to calcium ionophore.




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