Literature DB >> 6098668

The role of phosphatidylinositol 4,5 bisphosphate breakdown in cell-surface receptor activation.

C J Kirk, E A Bone, S Palmer, R H Michell.   

Abstract

The activation of Ca2+-mobilising receptors on hepatocytes and many other cells leads to a prompt reduction in the cellular content of inositol phospholipids. The primary event which underlies these changes is, most probably, a phospholipase C-catalysed attack upon phosphatidylinositol 4,5 bisphosphate. The receptor-mediated breakdown of this lipid in stimulated cells is: (i) not mediated by an increase in cytosol [Ca2+] and (ii) closely coupled to receptor occupation. Phosphatidylinositol 4,5 bisphosphate degradation may be studied by measuring the appearance of the water-soluble product, inositol trisphosphate (and its metabolites: inositol bisphosphate and inositol monophosphate), in stimulated cells. Recent evidence indicates that inositol trisphosphate and the lipid soluble product of phosphatidylinositol 4,5 bisphosphate breakdown, 1,2 diacylglycerol, may act as 'second messengers' which mediate the effects of many extracellular signals in stimulated cells.

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Year:  1984        PMID: 6098668     DOI: 10.3109/10799898409042569

Source DB:  PubMed          Journal:  J Recept Res        ISSN: 0197-5110


  9 in total

1.  Phosphatidylinositol 4,5-bisphosphate phospholipase C activity in particulate preparations from rat brain.

Authors:  M Bergers; S Lendi; P D Mier
Journal:  Lipids       Date:  1989-01       Impact factor: 1.880

2.  Characterization of specific V1a vasopressin-binding sites on a rat mammary-tumour-cell line.

Authors:  G Guillon; C J Kirk; M N Balestre
Journal:  Biochem J       Date:  1986-11-15       Impact factor: 3.857

3.  Effect of cyclic AMP-dependent hormones and Ca2+-mobilizing hormones on the Ca2+ influx and polyphosphoinositide metabolism in isolated rat hepatocytes.

Authors:  J Poggioli; J P Mauger; M Claret
Journal:  Biochem J       Date:  1986-05-01       Impact factor: 3.857

4.  Glucagon and vasopressin interactions on Ca2+ movements in isolated hepatocytes.

Authors:  L Combettes; B Berthon; A Binet; M Claret
Journal:  Biochem J       Date:  1986-08-01       Impact factor: 3.857

5.  The labelling of polyphosphoinositides with [32P]Pi and the accumulation of inositol phosphates in vasopressin-stimulated hepatocytes.

Authors:  S Palmer; P T Hawkins; R H Michell; C J Kirk
Journal:  Biochem J       Date:  1986-09-01       Impact factor: 3.857

Review 6.  Phosphoinositides: lipid regulators of membrane proteins.

Authors:  Björn H Falkenburger; Jill B Jensen; Eamonn J Dickson; Byung-Chang Suh; Bertil Hille
Journal:  J Physiol       Date:  2010-06-02       Impact factor: 5.182

7.  Kinetics of diacylglycerol accumulation in response to vasopressin stimulation in hepatocytes of continuously endotoxaemic rats.

Authors:  E B Rodriguez de Turco; J A Spitzer
Journal:  Biochem J       Date:  1988-07-01       Impact factor: 3.857

8.  Stimulation, by vasopressin and other agonists, of inositol-lipid breakdown and inositol phosphate accumulation in WRK 1 cells.

Authors:  C J Kirk; G Guillon; M N Balestre; S Jard
Journal:  Biochem J       Date:  1986-11-15       Impact factor: 3.857

9.  Striking a balance: PIP2 and PIP3 signaling in neuronal health and disease.

Authors:  Kamran Tariq; Bryan W Luikart
Journal:  Explor Neuroprotective Ther       Date:  2021-10-29
  9 in total

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