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Group V phospholipase A(2)-mediated oleic acid mobilization in lipopolysaccharide-stimulated P388D(1) macrophages

J Balsinde1, M A Balboa, S Yedgar

  • 1Department of Chemistry and Biochemistry, University of California at San Diego, La Jolla, California 92093-0601, USA. jbalsinde@ucsd.edu

Insights

Bacterial lipopolysaccharide (LPS) stimulates macrophages to release oleic acid (OA), similar to arachidonic acid (AA) release. This process involves secretory phospholipase A(2) (sPLA(2)) and cytosolic phospholipase A(2) (cPLA(2)).

Area of Science:

  • Cell Biology
  • Biochemistry
  • Immunology

Background:

  • Macrophages play a crucial role in immune responses.
  • Bacterial lipopolysaccharide (LPS) is a potent activator of macrophages.
  • Phospholipase A(2) (PLA(2)) enzymes are key in lipid mediator synthesis.

Purpose of the Study:

  • To investigate the release of oleic acid (OA) from LPS-stimulated macrophages.
  • To determine the enzymes involved in OA mobilization and release.
  • To compare OA release mechanisms with those of arachidonic acid (AA) release.

Main Methods:

  • P388D(1) macrophages were prelabeled with [(3)H]oleic acid (OA) or [(3)H]arachidonic acid (AA).
  • Cells were stimulated with bacterial lipopolysaccharide (LPS).
  • OA and AA release were measured, along with the effects of specific sPLA(2) and cPLA(2) inhibitors.

Main Results:

  • LPS stimulation induced the release of OA from macrophages.
  • OA release kinetics and concentration dependence mirrored those of AA release.
  • OA release was inhibited by sPLA(2) inhibitors and methyl arachidonyl fluorophosphonate, implicating both sPLA(2) and cPLA(2).

Conclusions:

  • A functionally active secretory phospholipase A(2) (sPLA(2)) is essential for LPS-induced OA release.
  • Group IV cytosolic phospholipase A(2) (cPLA(2)) also participates in OA release.
  • The regulatory mechanisms for OA release are similar to those observed for AA release in LPS-stimulated macrophages.

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