Literature DB >> 8396958

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

D A Foster1.   

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.

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Year:  1993        PMID: 8396958     DOI: 10.1016/0898-6568(93)90078-z

Source DB:  PubMed          Journal:  Cell Signal        ISSN: 0898-6568            Impact factor:   4.315


  8 in total

1.  Evidence that v-Src-induced phospholipase D activity is mediated by a G protein.

Authors:  H Jiang; K Alexandropoulos; J Song; D A Foster
Journal:  Mol Cell Biol       Date:  1994-06       Impact factor: 4.272

2.  Possible involvement of a tyrosine kinase-dependent pathway in the regulation of phosphoinositide metabolism by vanadate in normal mouse islets.

Authors:  J C Jonas; J C Henquin
Journal:  Biochem J       Date:  1996-04-01       Impact factor: 3.857

3.  Antagonistic effects of protein kinase C alpha and delta on both transformation and phospholipase D activity mediated by the epidermal growth factor receptor.

Authors:  A Hornia; Z Lu; T Sukezane; M Zhong; T Joseph; P Frankel; D A Foster
Journal:  Mol Cell Biol       Date:  1999-11       Impact factor: 4.272

4.  Functional association between Arf and RalA in active phospholipase D complex.

Authors:  J Q Luo; X Liu; P Frankel; T Rotunda; M Ramos; J Flom; H Jiang; L A Feig; A J Morris; R A Kahn; D A Foster
Journal:  Proc Natl Acad Sci U S A       Date:  1998-03-31       Impact factor: 11.205

5.  v-Src activates a unique phospholipase D activity that can be distinguished from the phospholipase D activity activated by phorbol esters.

Authors:  J Song; D A Foster
Journal:  Biochem J       Date:  1993-09-15       Impact factor: 3.857

6.  Ral-GTPases mediate a distinct downstream signaling pathway from Ras that facilitates cellular transformation.

Authors:  T Urano; R Emkey; L A Feig
Journal:  EMBO J       Date:  1996-02-15       Impact factor: 11.598

7.  Growth inhibition, enhancement of intercellular adhesion, and increased expression of carcinoembryonic antigen by overexpression of phosphoinositides-specific phospholipase C beta 1 in LS174T human colon adenocarcinoma cell line.

Authors:  K Nomoto; N Tomita; M Miyake; D B Xhu; P R LoGerfo; I B Weinstein
Journal:  Jpn J Cancer Res       Date:  1998-12

8.  Brain endothelial cell-cell junctions: how to "open" the blood brain barrier.

Authors:  Svetlana M Stamatovic; Richard F Keep; Anuska V Andjelkovic
Journal:  Curr Neuropharmacol       Date:  2008-09       Impact factor: 7.363

  8 in total

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