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PMID: 7834738 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Review

Specificity of receptor tyrosine kinase signaling: transient versus sustained extracellular signal-regulated kinase activation.

Cell ·Vol. 80 ·No. 2 ·1995-01-27 ·Pages 179-85

Marshall CJ

Abstract

A number of different intracellular signaling pathways have been shown to be activated by receptor tyrosine kinases. These activation events include the phosphoinositide 3-kinase, 70 kDa S6 kinase, mitogen-activated protein kinase (MAPK), phospholipase C-gamma, and the Jak/STAT pathways. The precise role of each of these pathways in cell signaling remains to be resolved, but studies on the differentiation of mammalian PC12 cells in tissue culture and the genetics of cell fate determination in Drosophila and Caenorhabditis suggest that the extracellular signal-regulated kinase (ERK-regulated) MAPK pathway may be sufficient for these cellular responses. Experiments with PC12 cells also suggest that the duration of ERK activation is critical for cell signaling decisions.

MeSH Terms
Animals Caenorhabditis Calcium-Calmodulin-Dependent Protein Kinases/metabolism Drosophila Enzyme Activation Humans Mitogen-Activated Protein Kinase Kinases PC12 Cells Phosphatidylinositol 3-Kinases Phosphotransferases (Alcohol Group Acceptor)/metabolism Protein Kinases/metabolism Protein Serine-Threonine Kinases/metabolism Protein-Tyrosine Kinases/metabolism Rats Receptor Protein-Tyrosine Kinases/metabolism Ribosomal Protein S6 Kinases Signal Transduction Substrate Specificity Type C Phospholipases/metabolism
Chemicals
Protein Kinases Phosphotransferases (Alcohol Group Acceptor) Protein-Tyrosine Kinases Receptor Protein-Tyrosine Kinases Protein Serine-Threonine Kinases Ribosomal Protein S6 Kinases Calcium-Calmodulin-Dependent Protein Kinases Mitogen-Activated Protein Kinase Kinases Type C Phospholipases
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Marshall C J
Chester Beatty Laboratories, Institute of Cancer Research, London, England.
Article Info
Journal
Cell
Abbr.
Cell
ISSN
0092-8674
Published
1995-01-27
Pages
179-85
Language
English
Region
United States
NLM ID
0413066
Subset
IM
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