Metabolism of platelet-activating factor in human platelets. Transacylase-mediated synthesis of 1-O-alkyl-2-arachidonoyl-sn-glycero-3-phosphocholine.

作者: R M Kramer , G M Patton , C R Pritzker , D Deykin

DOI: 10.1016/S0021-9258(18)90696-4

关键词:

摘要: The present study demonstrates that inactivation of exogenous 1-O-alkyl-2-acetyl-sn-glycero-3-phosphocholine (alkylacetyl-GPC; platelet-activating factor) by human platelets is mediated the sequential action two enzymes, 1) a Ca2+-independent acetylhydrolase recovered in cytosolic fraction deacylates alkylacetyl-GPC forming alkyllyso-GPC and 2) CoA-independent, N-ethylmaleimide-sensitive transacylase associated with platelet membranes incorporates long-chain fatty acid into to produce alkylacyl-GPC. Separation phospholipids subsequent resolution individual molecular species high-performance liquid chromatography revealed newly formed alkylacyl-GPC was exclusively alkylarachidonoyl-GPC arachidonoyl group for acylation provided phosphatidylcholine. We conclude previously described (Kramer, R.M., Deykin, D. (1983) J. Biol. Chem. 258, 13806-13811) may play an important role metabolism factor.

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