Thrombin and lysophosphatidic acid receptors utilize distinct rhoGEFs in prostate cancer cells

被引:59
作者
Wang, Q
Liu, M
Kozasa, T
Rothstein, JD
Sternweis, PC
Neubig, RR [1 ]
机构
[1] Univ Michigan, Dept Pharmacol, Ann Arbor, MI 48109 USA
[2] Univ Illinois, Dept Pharmacol, Chicago, IL 60612 USA
[3] Johns Hopkins Univ, Dept Neurol, Baltimore, MD 21287 USA
[4] Univ Texas, SW Med Ctr, Dept Pharmacol, Dallas, TX 75390 USA
关键词
D O I
10.1074/jbc.C400105200
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
Thrombin and lysophosphatidic acid (LPA) receptors play important roles in vascular biology, development, and cancer. These receptors activate rho via G(12/13) family heterotrimeric G proteins, which are known to directly activate three distinct rho guanine nucleotide exchange factors ( rhoGEFs) that contain a regulator of G protein signaling (RGS) domain (RGS-rhoGEFs). However, it is not known which, if any, of these RGS-rhoGEFs ( LARG (leukemia-associated rhoGEF), p115rhoGEF, or PDZrhoGEF) plays a role in G protein-coupled receptor-stimulated rho signaling. Using oligonucleotide small interfering RNAs that suppress specific RGS-rhoGEF expression, we show that thrombin receptor stimulation of rho is primarily mediated by LARG in HEK293T and PC-3 prostate cancer cell lines. In contrast, the LPA-stimulated rho response in PC-3 cells is dependent on PDZrhoGEF expression. Suppression of p115rhoGEF had no effect. Thus different rhoGEFs ( LARG and PDZrhoGEF) mediate downstream rho signaling by the thrombin and LPA receptors.
引用
收藏
页码:28831 / 28834
页数:4
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