ATRAP, novel AT1 receptor associated protein, enhances internalization of AT1 receptor and inhibits vascular smooth muscle cell growth

被引:64
作者
Cui, TX
Nakagami, H
Iwai, M
Takeda, Y
Shiuchi, T
Tamura, K
Daviet, L
Horiuchi, M [1 ]
机构
[1] Ehime Univ, Sch Med, Dept Med Biochem, Shigenobu, Ehime 7910295, Japan
[2] Yokohama City Univ, Sch Med, Dept Internal Med, Yokohama, Kanagawa 232, Japan
[3] Hybrigen SA, Paris, France
关键词
angiotensin; desensitization; internalization; receptor; vascular smooth muscle cell;
D O I
10.1006/bbrc.2000.4055
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 have identified a novel, membrane-located protein that interacts specifically with the carboxyl-terminal cytoplasmic domain of the AT1a receptor, which we named ATRAP (for AT1 receptor-associated protein). To further investigate the role of ATRAP in AT1 receptor function, we examined the effect of over-expression of ATRAP on angiotensin II (Ang II)induced AT1 receptor desensitization and/or internalization, and cell proliferation in adult vascular smooth muscle cells (VSMCs). Transfection of ATARP potentiated AT1 receptor internalization upon Ang II stimulation in these VSMCs. Moreover, we observed that AT1 receptor-induced DNA synthesis was markedly inhibited in ATRAP transfected VSMCs associated with the inhibition of the phosphorylation of signal transducers and activators of transcription (STAT) 3 and Akt, Our results suggest that ATRAP functions as a negative regulator in AT1 receptor-mediated cell proliferation in VSMCs. (C) 2000 Academic Press.
引用
收藏
页码:938 / 941
页数:4
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