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PMID: 7504324 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Activation of exocytosis by the heterotrimeric G protein Gi3.

Science (New York, N.Y.) ·Vol. 262 ·No. 5139 ·1993-12-03 ·Pages 1569-72

Aridor M, Rajmilevich G, Beaven MA, Sagi-Eisenberg R

Abstract

Secretagogues of rat peritoneal mast cells, such as mastoparan and compound 48/80, induce mast cell exocytosis by activating directly the guanosine triphosphate-binding proteins that are required for exocytosis. The introduction of a synthetic peptide that corresponds to the carboxyl-terminal end sequence of G alpha i3 into the cells specifically blocked this secretion. Similar results were obtained when antibodies to this peptide were introduced. The G alpha i3 was located in both the Golgi and the plasma membrane, but only the latter source of G alpha i3 appeared to be essential for secretion. These results indicate that G alpha i3 functions to control regulated exocytosis in mast cells.

MeSH Terms
Amino Acid Sequence Animals Exocytosis/drug effects,physiology GTP-Binding Proteins/analysis,drug effects,physiology Histamine Release/drug effects In Vitro Techniques Mast Cells/chemistry,drug effects,metabolism Molecular Sequence Data Peptide Fragments/pharmacology Rats Subcellular Fractions/chemistry Virulence Factors, Bordetella/pharmacology
Chemicals
Peptide Fragments Virulence Factors, Bordetella GTP-Binding Proteins
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Aridor M
Weizmann Institute of Science, Department of Chemical Immunology, Rehovot, Israel.
Rajmilevich G
Beaven M A
Sagi-Eisenberg R
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
0036-8075
Published
1993-12-03
Pages
1569-72
Language
English
Region
United States
NLM ID
0404511
Subset
IM
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