HYPOXIA INCREASES STIMULUS-INDUCED PAF PRODUCTION AND RELEASE FROM HUMAN UMBILICAL VEIN ENDOTHELIAL-CELLS

被引:32
作者
CAPLAN, MS [1 ]
ADLER, L [1 ]
KELLY, A [1 ]
WEI, H [1 ]
机构
[1] NORTHWESTERN UNIV,CHILDRENS MEM HOSP,SCH MED,DEPT PATHOL,CHICAGO,IL 60614
关键词
PAF; HYPOXIA; ENDOTHELIAL CELL; PHOSPHOLIPASE-A2; ACETYLHYDROLASE;
D O I
10.1016/0005-2760(92)90309-J
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
Hypoxia alters endothelial cell function and metabolism. Since PAF is synthesized by endothelial cells and capable of modulating endothelial cell responses, we investigated the effect of hypoxia on synthesis and release of PAF from endothelial cells. We found: (1) Approx. 90% of the radylPAF derivative in stimulated endothelial cells is acylPAF. (2) Acute hypoxic (15 min-1 h) priming increased ionophore- and thrombin-induced radylPAF accumulation. (3) Long-term hypoxic exposure increased radylPAF accumulation at 24 and 48 h in the presence of ionophore. (4) Bioactive PAF was released into media and hypoxia and ionophore synergistically increased PAF release. (5) Hypoxia and ionophore stimulation increased phospholipase A2 activity and decreased acetylhydrolase activity in endothelial cells. We conclude that hypoxia and ionophore increase PAF synthesis and release from endothelial cells.
引用
收藏
页码:205 / 210
页数:6
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