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Localized Mast Cell Degranulation Induced by Concanavalin A-sepharose Beads. Implications for the Ca2+ Hypothesis of Stimulus-secretion Coupling

Overview
Journal J Cell Biol
Specialty Cell Biology
Date 1978 Nov 1
PMID 569156
Citations 16
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Abstract

Concanavalin A (Con A) covalently linked to Sepharose 4B beads induced localized degranulation of sensitized rat peritoneal mast cells in regions of contact between beads and cells. This degranulation was Ca2+ dependent and was not seen when sensitized mast cells bound to beads conjugated with a nonstimulating lectin, wheat germ agglutinin, or when unsensitized mast cells bound to Con A-Sepharose. The finding that sensitized mast cells which had adhered to Con A-Sepharose beads degranulated in regions of the cell away from the area of bead contact if exposed to soluble Con A excluded the possibility that the localized release was due to a redistribution of the IgE receptors or putative Ca2+ channels to the region of bead contact. The results suggest that, if an influx of Ca2+ is the mechanism for initiating mast cell degranulation, then the opening of Ca2+ channels in the plasma membrane of activated mast cells is a localized event and that Ca2+ acts locally within the cell to initiate exocytosis.

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References
1.
Kanno T, Cochrane D, DOUGLAS W . Exocytosis (secretory granule extrusion) induced by injection of calcium into mast cells. Can J Physiol Pharmacol. 1973; 51(12):1001-4. DOI: 10.1139/y73-153. View

2.
Hino R, Lau C, READ G . The site of action of the histamine releaser compound 45/80 in causing mast cell degranulation. J Pharmacol Exp Ther. 1977; 200(3):658-63. View

3.
Lawson D, Raff M, Gomperts B, Fewtrell C, Gilula N . Molecular events during membrane fusion. A study of exocytosis in rat peritoneal mast cells. J Cell Biol. 1977; 72(2):242-59. PMC: 2111007. DOI: 10.1083/jcb.72.2.242. View

4.
Tasaka K, Yamasaki H . Local degranulation and histamine release from a single rat mast cell by microelectrophoretic application of basic histamine releasers and antigen. Acta Derm Venereol Suppl (Stockh). 1973; 73:167-73. View

5.
Foreman J, Garland L . Desensitization in the process of histamine secretion induced by antigen and dextran. J Physiol. 1974; 239(2):381-91. PMC: 1330929. DOI: 10.1113/jphysiol.1974.sp010574. View