Literature DB >> 16962823

Biochemical properties and pathophysiological roles of cytosolic phospholipase A2s.

Yoshihiro Kita1, Takayo Ohto, Naonori Uozumi, Takao Shimizu.   

Abstract

Phospholipase A(2) (PLA(2)) (EC 3.1.1.4) catalyzes hydrolysis of the sn-2 ester bond of glycerophospholipids. The enzyme is essential for the production of two classes of lipid mediators, fatty acid metabolites and lysophospholipid-related lipids, as well as being involved in the remodeling of membrane phospholipids. Among many mammalian PLA(2)s, cytosolic PLA(2)alpha (cPLA(2)alpha) plays a critical role in various physiological and pathophysiological conditions through generating lipid mediators. Here, we summarize the in vivo significance of cPLA(2)alpha, revealed from the phenotypes of cPLA(2)alpha-null mice, and properties of newly discovered cPLA(2) family enzymes. We also briefly introduce a quantitative lipidomics strategy using liquid chromatography-mass spectrometry, a powerful tool for the comprehensive analysis of lipid mediators.

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Year:  2006        PMID: 16962823     DOI: 10.1016/j.bbalip.2006.08.001

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  34 in total

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4.  Disruption of group IVA cytosolic phospholipase A(2) attenuates myocardial ischemia-reperfusion injury partly through inhibition of TNF-α-mediated pathway.

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6.  Phospholipases of mineralization competent cells and matrix vesicles: roles in physiological and pathological mineralizations.

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Journal:  Mol Pharmacol       Date:  2009-07-14       Impact factor: 4.436

8.  Genetic interactions between a phospholipase A2 and the Rim101 pathway components in S. cerevisiae reveal a role for this pathway in response to changes in membrane composition and shape.

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Journal:  Mol Genet Genomics       Date:  2010-04-09       Impact factor: 3.291

9.  Smooth muscle cell arachidonic acid release, migration, and proliferation are markedly attenuated in mice null for calcium-independent phospholipase A2beta.

Authors:  Sung Ho Moon; Christopher M Jenkins; David J Mancuso; John Turk; Richard W Gross
Journal:  J Biol Chem       Date:  2008-10-16       Impact factor: 5.157

10.  Amyloid-beta42 signals tau hyperphosphorylation and compromises neuronal viability by disrupting alkylacylglycerophosphocholine metabolism.

Authors:  Scott D Ryan; Shawn N Whitehead; Leigh Anne Swayne; Tia C Moffat; Weimin Hou; Martin Ethier; André J G Bourgeois; Juliet Rashidian; Alexandre P Blanchard; Paul E Fraser; David S Park; Daniel Figeys; Steffany A L Bennett
Journal:  Proc Natl Acad Sci U S A       Date:  2009-11-19       Impact factor: 11.205

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