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PMID: 6204890 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Islet-activating protein, pertussis toxin, inhibits Ca2+-induced and guanine nucleotide-dependent releases of histamine and arachidonic acid from rat mast cells.

FEBS letters ·Vol. 173 ·No. 2 ·1984-08-06 ·Pages 414-8

Nakamura T, Ui M

Abstract

Islet-activating protein (IAP) suppressed Ca2+-induced histamine release and phospholipase A2 activation in Gpp(NH)p-loaded mast cells. Since the guanine nucleotide-binding protein involved in adenylate cyclase inhibition is known to lose its function upon being ADP-ribosylated by IAP, the nucleotide-binding protein is likely to mediate Ca2+-linked biosignalling leading to histamine secretion.

MeSH Terms
Adenylate Cyclase Toxin Adenylyl Cyclases/metabolism Animals Arachidonic Acid Arachidonic Acids/metabolism Bacterial Proteins/pharmacology Bacterial Toxins/pharmacology Calcium/pharmacology GTP-Binding Proteins Guanosine Triphosphate/analogs & derivatives Guanylyl Imidodiphosphate/pharmacology Histamine Release/drug effects In Vitro Techniques Kinetics Mast Cells/drug effects,immunology,physiology Pertussis Toxin Rats Receptors, Cell Surface/metabolism Virulence Factors, Bordetella
Chemicals
Adenylate Cyclase Toxin Arachidonic Acids Bacterial Proteins Bacterial Toxins Receptors, Cell Surface Virulence Factors, Bordetella Arachidonic Acid Guanylyl Imidodiphosphate Guanosine Triphosphate Pertussis Toxin GTP-Binding Proteins Adenylyl Cyclases Calcium
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Nakamura T
Ui M
Article Info
Journal
FEBS letters
Abbr.
FEBS Lett
ISSN
0014-5793
Published
1984-08-06
Pages
414-8
Language
English
Region
England
NLM ID
0155157
Subset
IM
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