ISOLATION OF A PHOSPHOLIPID INHIBITOR OF PLATELET ACTIVATING FACTOR-INDUCED ACTIVITY FROM PERFUSED-RAT-LIVER - IDENTIFICATION AS PHOSPHATIDYLGLYCEROL

被引:13
作者
LEKKA, M [1 ]
TOKUMURA, A [1 ]
TSUJI, H [1 ]
HANAHAN, DJ [1 ]
机构
[1] UNIV TEXAS,HLTH SCI CTR,DEPT BIOCHEM,SAN ANTONIO,TX 78284
关键词
D O I
10.1006/abbi.1993.1227
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
An endogenous inhibitor of platelet activating factor action was isolated from perfused rat liver. It was purified by thin-layer chromatography and high-performance liquid chromatography and subjected to chemical modifications in order to identify its structure. On the basis of its fast atom bombardment-mass spectrum it was characterized as phosphatidylglycerol composed mainly of 16:0/18:1 and 16:0/20:2 fatty acyl chains ([M + H]+ at m/z 749 and 775, respectively) and very minor levels of 18:0/18:1 and 18:0/20:2. The purified compound exhibited inhibition on rabbit platelet aggregation induced by 5 x 10-10 M platelet activating factor (PAF) at an EC50 value near 2.5 x 10-6 M and on the serotonin secretion at an EC50 7 x 10-6 M. Other phospholipids isolated from the liver preparations, such as phosphatidylethanolamine, phosphatidylserine, phosphatidylinositol, sphingomyelin, cardiolipin (diphosphatidylglycerol), and phosphatidic acid, exhibited no inhibitory activity in the concentration range from 1 x 10-4 to 1 x 10-7 M nor did they induce any aggregation, or lysis, of the platelets. Of importance, phosphatidylglycerol could inhibit thrombin- and ADP-induced aggregation of rabbit platelets. These results suggested a possible site of inhibition common to the signal transduction pathway of these agonists. Preliminary binding experiments showed a noncompetitive type of inhibition on PAF binding to intact rabbit platelets. © 1993 Academic Press, Inc.
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页码:380 / 384
页数:5
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