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PMID: 8396958 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S. Review

Intracellular signalling mediated by protein-tyrosine kinases: networking through phospholipid metabolism.

Cellular signalling ·Vol. 5 ·No. 4 ·1993-07-00 ·Pages 389-99

Foster DA

Abstract

In recent years, it has become apparent that receptor-mediated intracellular signals are not linear cascades beginning at the plasma membrane and terminating with the production of a needed metabolite or the induction of gene expression. Instead, complex networks of interactive intracellular signals are activated in response to extracellular stimuli. Many responses to extracellular stimuli are mediated by protein-tyrosine kinases (PTKs). Activating PTKs leads to the recruitment of a variety of intracellular signalling molecules that execute a complex set of instructions. The response to PTK activity is dependent upon which PTK is activated and the cellular context in which the PTK exists. Several signalling molecules recruited by PTKs are involved in the metabolism of phospholipids. In this Mini Review, intracellular signalling networks activated by PTKs are discussed with an emphasis on the potential for generating highly specific and sophisticated responses to PTK activity through phospholipid metabolism.

MeSH Terms
Animals Cell Division Enzyme Activation Phosphatidylinositol 3-Kinases Phospholipids/metabolism Phosphotransferases/metabolism Protein-Tyrosine Kinases/metabolism Receptors, Cell Surface/metabolism Signal Transduction Type C Phospholipases/metabolism
Chemicals
Phospholipids Receptors, Cell Surface Phosphotransferases Phosphatidylinositol 3-Kinases Protein-Tyrosine Kinases Type C Phospholipases
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Foster D A
Institute for Biomolecular Structure and Function, Hunter College, City University of New York, NY 10021.
Article Info
Journal
Cellular signalling
Abbr.
Cell Signal
ISSN
0898-6568
Published
1993-07-00
Pages
389-99
Language
English
Region
England
NLM ID
8904683
Subset
IM
Grants
NCI NIH HHS · CA46677 · United States
NCRR NIH HHS · RRO-3037-03 · United States
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