Literature DB >> 8212322

Desensitization of cell signalling mediated by phosphoinositidase C.

R J Wojcikiewicz1, A B Tobin, S R Nahorski.   

Abstract

The waning of responses to cell-surface receptor activation during persistent stimulation with agonists (desensitization) is a feature common to many forms of transmembrane signalling. However, information is scarce regarding the regulatory processes that modulate the extensive group of receptors linked via phosphoinositidase C to the production of inositol 1,4,5-trisphosphate and 1,2-diacylglycerol. This situation is now beginning to change. Recent data indicate (1) that very rapid desensitization, possibly associated with receptor phosphorylation, regulates receptors linked to phosphoinositidase C, (2) that different receptors are desensitized to varying extents, (3) that receptor internalization can mediate desensitization at later times and (4) that signalling can be regulated at additional sites downstream of phosphoinositidase C. As Richard Wojcikiewicz and colleagues discuss here, these diverse regulatory events provide the means by which the breakdown of phosphoinositides and cellular responsiveness to their products are controlled during cell stimulation.

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Year:  1993        PMID: 8212322     DOI: 10.1016/0165-6147(93)90131-3

Source DB:  PubMed          Journal:  Trends Pharmacol Sci        ISSN: 0165-6147            Impact factor:   14.819


  24 in total

1.  Down-regulation of types I, II and III inositol 1,4,5-trisphosphate receptors is mediated by the ubiquitin/proteasome pathway.

Authors:  J Oberdorf; J M Webster; C C Zhu; S G Luo; R J Wojcikiewicz
Journal:  Biochem J       Date:  1999-04-15       Impact factor: 3.857

2.  Role of sarcoplasmic/endoplasmic-reticulum Ca2+-ATPases in mediating Ca2+ waves and local Ca2+-release microdomains in cultured glia.

Authors:  P B Simpson; J T Russell
Journal:  Biochem J       Date:  1997-07-01       Impact factor: 3.857

3.  Desensitization of P2U receptor in neuronal cell line. Different control by the agonists ATP and UTP, as demonstrated by single-cell Ca2+ responses.

Authors:  U Czubayko; G Reiser
Journal:  Biochem J       Date:  1996-11-15       Impact factor: 3.857

4.  Agonist-induced desensitization and phosphorylation of m1-muscarinic receptors.

Authors:  M G Waugh; R A Challiss; G Berstein; S R Nahorski; A B Tobin
Journal:  Biochem J       Date:  1999-02-15       Impact factor: 3.857

5.  Pharmacological characterization of desensitization in a human mGlu1 alpha-expressing non-neuronal cell line co-transfected with a glutamate transporter.

Authors:  M A Desai; J P Burnett; N G Mayne; D D Schoepp
Journal:  Br J Pharmacol       Date:  1996-07       Impact factor: 8.739

6.  High concentrations of tricyclic antidepressants increase intracellular Ca2+ in cultured neural cells.

Authors:  P G Joshi; A Singh; B Ravichandra
Journal:  Neurochem Res       Date:  1999-03       Impact factor: 3.996

7.  The activation of metabotropic glutamate receptors protects nerve cells from oxidative stress.

Authors:  Y Sagara; D Schubert
Journal:  J Neurosci       Date:  1998-09-01       Impact factor: 6.167

8.  Depletion-activated calcium current is inhibited by protein kinase in RBL-2H3 cells.

Authors:  A B Parekh; R Penner
Journal:  Proc Natl Acad Sci U S A       Date:  1995-08-15       Impact factor: 11.205

9.  The histamine H1 receptor in GT1-7 neuronal cells is regulated by calcium influx and KN-62, a putative inhibitor of calcium/calmodulin protein kinase II.

Authors:  M R Zamani; D R Bristow
Journal:  Br J Pharmacol       Date:  1996-07       Impact factor: 8.739

10.  Characterization of metabotropic glutamate receptor-mediated facilitation of N-methyl-D-aspartate depolarization of neocortical neurones.

Authors:  S Rahman; R S Neuman
Journal:  Br J Pharmacol       Date:  1996-02       Impact factor: 8.739

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