Suppr超能文献

通过使用受体嵌合体鉴定血管紧张素II 1型受体中决定与Gq偶联的结构域。

Identification of a domain in the angiotensin II type 1 receptor determining Gq coupling by the use of receptor chimeras.

作者信息

Wang C, Jayadev S, Escobedo J A

机构信息

Cardiovascular Research Institute, University of California, San Francisco 94143-0130, USA.

出版信息

J Biol Chem. 1995 Jul 14;270(28):16677-82. doi: 10.1074/jbc.270.28.16677.

Abstract

The angiotensin II type 1 (AT1R) and type 2 (AT2R) receptors belong to the seven transmembrane receptor superfamily. Previous studies have suggested that the AT1R couples to a Gq signaling pathway, whereas the AT2R does not associate with Gq. To identify the role that individual intracellular domains play in AT1R function, AT1R/AT2R chimeric receptors were prepared by substitution of intracellular loops. CHO cells expressing these chimeras were used to test angiotensin II-induced c-fos expression and Ca2+ mobilization which are involved in the AT1R signaling pathway through Gq coupling. Substitution of the second intracellular loop (IC2) and the cytoplasmic tail between the two receptors did not affect AT1R function. However, exchange of the third intracellular loop (IC3) resulted in the loss of function in the AT1R and conferred to the AT2R the ability to constitutively activate the fos promoter. These findings suggest that the third intracellular loop of the AT1R is critical for Gq coupling. Substitution of discrete amino acid sequences of the third intracellular loop indicate that its N-terminal and C-terminal portions, especially the seven amino acids 219-225 in the N-terminal portion, are important for AT1R function, and that the intermediate portion of this loop is not required for Gq coupling.

摘要

血管紧张素 II 1型(AT1R)和2型(AT2R)受体属于七跨膜受体超家族。先前的研究表明,AT1R与Gq信号通路偶联,而AT2R不与Gq相关联。为了确定各个细胞内结构域在AT1R功能中所起的作用,通过替换细胞内环制备了AT1R/AT2R嵌合受体。使用表达这些嵌合体的CHO细胞来测试血管紧张素II诱导的c-fos表达和Ca2+动员,它们通过Gq偶联参与AT1R信号通路。两个受体之间的第二细胞内环(IC2)和细胞质尾的替换不影响AT1R功能。然而,第三细胞内环(IC3)的交换导致AT1R功能丧失,并赋予AT2R组成性激活fos启动子的能力。这些发现表明,AT1R的第三细胞内环对于Gq偶联至关重要。第三细胞内环离散氨基酸序列的替换表明,其N端和C端部分,特别是N端部分的七个氨基酸219-225,对AT1R功能很重要,并且该环的中间部分对于Gq偶联不是必需的。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验