Apelin (65-77) activates extracellular signal-regulated kinases via a PTX-sensitive G protein

被引:140
作者
Masri, B
Lahlou, H
Mazarguil, H
Knibiehler, B
Audigier, Y
机构
[1] CHU Rangueil, Unite INSERM U 397, F-31403 Toulouse, France
[2] CHU Rangueil, Unite INSERM U 531, F-31403 Toulouse, France
[3] Inst Pharmacol & Biol Struct, F-31077 Toulouse, France
关键词
G protein-coupled receptors; phosphorylation cascades; endothelium; vertebrate; mouse;
D O I
10.1006/bbrc.2001.6230
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
We report here that apelin (65-77) induces activation of extracellular-regulated kinases (ERKs) in Chinese hamster ovary (CHO) cells expressing the msr/apj receptor. This concentration-dependent activation was transient, peaking at 5 min. Pretreatment of CHO cells with pertussis toxin fully abrogated ERK phosphorylation, whereas overexpression of the beta-adrenergic receptor kinase-1 C-terminal fragment did not alter ERK activation. Transfection with a dominant-negative mutant of Ras was without effect on ERK activation, whereas an inhibitor of many protein kinase C isoforms, GF109203X, strongly decreased it. These results demonstrate that stimulation of the murine msr/apj receptor promotes ERK activation via the a subunit of a pertussis toxin-sensitive protein in a Ras-independent pathway. (C) 2002 Elsevier Science.
引用
收藏
页码:539 / 545
页数:7
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