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PMID: 2163543 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Intracellular calcium release mediated by sphingosine derivatives generated in cells.

Science (New York, N.Y.) ·Vol. 248 ·No. 4963 ·1990-06-29 ·Pages 1653-6

Ghosh TK, Bian J, Gill DL

Abstract

Soluble and hydrophobic lipid breakdown products have a variety of important signaling roles in cells. Here sphingoid bases derived in cells from sphingolipid breakdown are shown to have a potent and direct effect in mediating calcium release from intracellular stores. Sphingosine must be enzymically converted within the cell to a product believed to be sphingosine-1-phosphate, which thereafter effects calcium release from a pool including the inositol 1,4,5-trisphosphate-sensitive calcium pool. The sensitivity, molecular specificity, and reversibility of the effect on calcium movements closely parallel sphingoid base-mediated inhibition of protein kinase C. Generation of sphingoid bases in cells may activate a dual signaling pathway involving regulation of calcium and protein kinase C, comparable perhaps to the phosphatidylinositol and calcium signaling pathway.

MeSH Terms
Adenosine Diphosphate/pharmacology Animals Calcimycin/pharmacology Calcium/metabolism Cell Line Kinetics Phosphoric Monoester Hydrolases/metabolism Phosphorylcholine/analogs & derivatives,pharmacology Protein Kinase C/metabolism Second Messenger Systems/drug effects Sphingosine/analogs & derivatives,pharmacology Thermodynamics
Chemicals
sphingosine phosphorylcholine Phosphorylcholine Calcimycin Adenosine Diphosphate Protein Kinase C mannose-6-phosphatase Phosphoric Monoester Hydrolases Sphingosine Calcium
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Ghosh T K
Department of Biological Chemistry, University of Maryland School of Medicine, Baltimore 21201.
Bian J
Gill D L
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
0036-8075
Published
1990-06-29
Pages
1653-6
Language
English
Region
United States
NLM ID
0404511
Subset
IM
Grants
NINDS NIH HHS · NS19304 · United States
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