Enzymatic properties of human cytosolic phospholipase A(2)gamma

J Biol Chem. 2002 Aug 16;277(33):29526-36. doi: 10.1074/jbc.M204856200. Epub 2002 May 30.

Abstract

The enzymatic properties of cytosolic phospholipase A(2)gamma (cPLA(2)gamma), an isoform of 85-kDa group IV cPLA(2)alpha (cPLA(2)alpha) were studied in vitro and when the enzyme was expressed in cells. cPLA(2)gamma expressed in Sf9 cells is associated with membrane. Membranes isolated from [(3)H]arachidonic acid-labeled Sf9 cells expressing cPLA(2)gamma, constitutively release [(3)H]arachidonic acid. The membrane-associated activity is inhibited by the group IV PLA(2) inhibitor methylarachidonyl fluorophosphonate, but not effectively by the group VI PLA(2) inhibitor (E)-6-(bromomethylene)-3-(1-naphthalenyl)-2H-tetrahydropyran-2-one. cPLA(2)gamma has higher lysophospholipase activity than PLA(2) activity. Purified His-cPLA(2)gamma does not exhibit phospholipase A(1) activity, but sequentially hydrolyzes fatty acid from the sn-2 and sn-1 positions of phosphatidylcholine. cPLA(2)gamma overexpressed in HEK293 cells is constitutively active in isolated membranes, releasing large amounts of oleic, arachidonic, palmitic, and stearic acids; however, basal fatty acid release from intact cells is not increased. cPLA(2)gamma overexpressed in lung fibroblasts from cPLA(2)alpha-deficient mice is activated by mouse serum resulting in release of arachidonic, oleic, and palmitic acids, whereas overexpression of cPLA(2)alpha results primarily in arachidonic acid release.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • Cell Line
  • Cloning, Molecular
  • Cytosol / enzymology*
  • DNA Primers
  • Enzyme Inhibitors / pharmacology
  • Fatty Acids / metabolism
  • Humans
  • Phospholipases A / antagonists & inhibitors
  • Phospholipases A / genetics
  • Phospholipases A / metabolism*
  • Recombinant Proteins / genetics
  • Recombinant Proteins / metabolism
  • Spodoptera

Substances

  • DNA Primers
  • Enzyme Inhibitors
  • Fatty Acids
  • Recombinant Proteins
  • Phospholipases A