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PMID: 9744561 Published · ppublish English Journal Article Review

Signaling from G-protein-coupled receptors to mitogen-activated protein (MAP)-kinase cascades.

Biochemical pharmacology ·Vol. 56 ·No. 3 ·1998-08-01 ·Pages 269-77

Lopez-Ilasaca M

Abstract

Heterotrimeric GTP-binding protein (G-protein)-coupled receptors are able to induce a variety of responses including cell proliferation, differentiation, and activation of several intracellular kinase cascades. Prominent among these kinases are the activation of mitogen-activated protein (MAP) kinase, including the extracellular signal-regulated kinases (ERKs), ERK1 and ERK2 (p44mapk and p42mapk, respectively); stress-activated protein kinases (SAPKs/JNKs); and p38 kinase. These receptors signal through G-proteins. Recent data have shown that the activation of mitogen-activated protein/ERK kinase induced by G-protein-coupled receptors is mediated by both Galpha and Gbetagamma subunits involving a common signaling pathway with receptor-tyrosine-kinases. Gbetagamma-mediated mitogen-activated protein kinase activation is mediated by activation of phosphoinositide 3-kinase, followed by a tyrosine phosphorylation event, and proceeds in a sequence of events that involve functional association among the adaptor proteins Shc, Grb2, and Sos. SAPKs/JNKs and p38 are able to be activated by Gbetagamma proteins in a pathway involving Rho family proteins including RhoA, Rac1, and Cdc42.

MeSH Terms
Animals Calcium-Calmodulin-Dependent Protein Kinases/metabolism Enzyme Activation GTP-Binding Proteins/physiology Humans JNK Mitogen-Activated Protein Kinases MAP Kinase Kinase 4 Mitogen-Activated Protein Kinase Kinases Phosphatidylinositol 3-Kinases/metabolism Protein Kinases/metabolism Signal Transduction
Chemicals
Protein Kinases Phosphatidylinositol 3-Kinases Calcium-Calmodulin-Dependent Protein Kinases JNK Mitogen-Activated Protein Kinases MAP Kinase Kinase 4 Mitogen-Activated Protein Kinase Kinases GTP-Binding Proteins
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Lopez-Ilasaca M
Max-Planck-Research Unit Molecular Cell Biology, Medical Faculty, University of Jena, Germany. mlopez@cbr.med.harvard.edu
Article Info
Journal
Biochemical pharmacology
Abbr.
Biochem Pharmacol
ISSN
0006-2952
Published
1998-08-01
Pages
269-77
Language
English
Region
England
NLM ID
0101032
Subset
IM
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