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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
Abstract:
P388D(1) macrophages prelabeled with [(3)H]arachidonic acid (AA) respond to bacterial lipopolysaccharide (LPS) by mobilizing AA in a process that takes several hours and is mediated by the concerted actions of the group IV cytosolic phospholipase A(2) and the group V secretory phospholipase A(2) (sPLA(2)). Here we show that when the LPS-activated cells are prelabeled with [(3)H]oleic acid (OA), they also mobilize and release OA to the extracellular medium. The time and concentration dependence of the LPS effect on OA release fully resemble those of the AA release. Experiments in which both AA and OA release are measured simultaneously indicate that AA is released 3 times more efficiently than OA. Importantly, LPS-stimulated OA release is strongly inhibited by the selective sPLA(2) inhibitors 3-(3-acetamide-1-benzyl-2-ethylindolyl-5-oxy)propane sulfonic acid and carboxymethylcellulose-linked phosphatidylethanolamine. The addition of exogenous recombinant sPLA(2) to the cells also triggers OA release. These data implicate a functionally active sPLA(2) as being essential for the cells to release OA upon stimulation with LPS. OA release is also inhibited by methyl arachidonyl fluorophosphonate but not by bromoenol lactone, indicating that the group IV cytosolic phospholipase A(2) is also involved in the process. Together, these data reveal that OA release occurs during stimulation of the P388D(1) macrophages by LPS and that the regulatory features of the OA release are strikingly similar to those previously found for the AA release.
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.