ENDOTHELIN-1 INDUCTION OF CYCLOOXYGENASE-2 EXPRESSION IN RAT MESANGIAL CELLS

被引:53
作者
HUGHES, AK
PADILLA, E
KUTCHERA, WA
MICHAEL, JR
KOHAN, DE
机构
[1] UNIV UTAH,MED CTR,SCH MED,DIV NEPHROL,SALT LAKE CITY,UT 84132
[2] UNIV UTAH,SCH MED,DIV CARDIOL,SALT LAKE CITY,UT 84132
[3] UNIV UTAH,SCH MED,DIV PULM DIS,SALT LAKE CITY,UT 84132
[4] VET AFFAIRS MED CTR,ECCLES PROGRAM HUMAN MOLEC BIOL & GENET,SALT LAKE CITY,UT
关键词
D O I
10.1038/ki.1995.6
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Prostaglandin E(2) (PGE(2)) may be an important negative feedback modulator of endothelin-1 (ET-1)-stimulated mesangial cell proliferation and contraction. Recent studies suggest that ET-1 may induce prolonged mesangial cell PGE(2) production, however the mechanism of this effect is unknown. The current study was undertaken, therefore, to examine the long-term effect of ET-1 on mesangial cell PGE(2) synthesis. ET-1 markedly increased PGE(2) release by rat mesangial cells for at least six hours. Cyclooxygenase (COX) activity was increased by one hour and persisted for at least six hours. ET-1 increased COX-2, but not COX-1, protein and mRNA levels. Actinomycin D reduced ET-1-stimulated PGE(2) synthesis and COX-2 mRNA expression, while cycloheximide superinduced COX-2 mRNA. Dexamethasone decreased ET-1-stimulated PGE(2) release and COX-2 protein and mRNA levels. ET-1-stimulated PGE(2) release was prevented by BQ-123, an endothelin receptor A antagonist. We conclude that ET-1, via activation of the endothelin A receptor, causes a prolonged increase in mesangial cell PGE(2) production that is partially dependent on induction of dexamethasone-inhibitable COX-2.
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页码:53 / 61
页数:9
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