Mechanical stress activates angiotensin II type 1 receptor without the involvement of angiotensin II

被引:519
作者
Zou, YZ
Akazawa, H
Qin, YJ
Sano, M
Takano, H
Minamino, T
Makita, N
Iwanaga, K
Zhu, WD
Kudoh, S
Toko, H
Tamura, K
Kihara, M
Nagai, T
Fukamizu, A
Umemura, S
Iiri, T
Fujita, T
Komuro, I
机构
[1] Chiba Univ, Grad Sch Med, Dept Cardiovasc Sci & Med, Chuo Ku, Chiba 2608670, Japan
[2] Univ Tokyo, Grad Sch Med, Dept Nephrol & Endocrinol, Bunkyo Ku, Tokyo 1138655, Japan
[3] Kanazawa Med Univ, Dept Cardiol, Kawakita, Ishikawa 9200265, Japan
[4] Yokohama City Univ, Sch Med, Dept Internal Med 2, Kanazawa Ku, Kanagawa 2360004, Japan
[5] Univ Tsukuba, Inst Appl Biochem, Ctr Tsukuba Adv Res Alliance, Tsukuba, Ibaraki 3058577, Japan
关键词
D O I
10.1038/ncb1137
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The angiotensin II type 1 (AT1) receptor has a crucial role in load-induced cardiac hypertrophy. Here we show that the AT1 receptor can be activated by mechanical stress through an angiotensin-II-independent mechanism. Without the involvement of angiotensin II, mechanical stress not only activates extracellular-signal-regulated kinases and increases phosphoinositide production in vitro, but also induces cardiac hypertrophy in vivo. Mechanical stretch induces association of the AT1 receptor with Janus kinase 2, and translocation of G proteins into the cytosol. All of these events are inhibited by the AT1 receptor blocker candesartan. Thus, mechanical stress activates AT1 receptor independently of angiotensin II, and this activation can be inhibited by an inverse agonist of the AT1 receptor.
引用
收藏
页码:499 / 506
页数:8
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