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Research Article Free access | 10.1172/JCI117141

Role of cytosolic calcium-independent plasmalogen-selective phospholipase A2 in hypoxic injury to rabbit proximal tubules.

D Portilla, S V Shah, P A Lehman, and M H Creer

Division of Nephrology, University of Arkansas for Medical Sciences, Little Rock 72205.

Find articles by Portilla, D. in: PubMed | Google Scholar

Division of Nephrology, University of Arkansas for Medical Sciences, Little Rock 72205.

Find articles by Shah, S. in: PubMed | Google Scholar

Division of Nephrology, University of Arkansas for Medical Sciences, Little Rock 72205.

Find articles by Lehman, P. in: PubMed | Google Scholar

Division of Nephrology, University of Arkansas for Medical Sciences, Little Rock 72205.

Find articles by Creer, M. in: PubMed | Google Scholar

Published April 1, 1994 - More info

Published in Volume 93, Issue 4 on April 1, 1994
J Clin Invest. 1994;93(4):1609–1615. https://doi.org/10.1172/JCI117141.
© 1994 The American Society for Clinical Investigation
Published April 1, 1994 - Version history
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Abstract

Although the activation of calcium-independent phospholipase A2 (PLA2) enzymes has been described in the heart, the pathogenetic role of this enzyme(s) in hypoxic cell injury has not been previously examined in any tissue. Therefore, we characterized the time course of activation of calcium-independent PLA2 using both plasmalogen and diacylglycerophospholipid substrates during hypoxia in rabbit proximal tubules and examined whether inhibition of calcium-independent PLA2 activity is associated with a cytoprotective effect. Subjecting rabbit proximal tubules to hypoxia for 5 min resulted in at least a threefold increase in cytosolic calcium-independent PLA2, which was selective for plasmalogen substrates (control 444 +/- 69 vs hypoxia 1,675 +/- 194 pmol.mg protein-1.min-1, n = 5). In contrast, no changes in PLA2 activity were observed in the presence of 4 mM EGTA in the membrane fraction using plasmenylcholine substrates. 20 min of hypoxia resulted in an increase in arachidonate from 3 +/- 1 to 28 +/- 4 ng/mg protein and lactate dehydrogenase release from 7.5 +/- 2% to 38 +/- 5%, n = 4. Pretreatment of proximal tubules with 10 microM Compound I, a specific inhibitor of calcium-independent PLA2, resulted in reduction in the magnitude of both hypoxia-induced arachidonic acid release (11 +/- 3 ng/mg protein) and lactate dehydrogenase release (18 +/- 4%). Our data indicate that a significant fraction of PLA2 activity in the proximal tubule is calcium-independent and selective for plasmalogen substrates. Furthermore, the activation of this enzyme plays an important role in the pathogenesis of membrane injury during hypoxia in the proximal tubule.

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