首页 | 本学科首页   官方微博 | 高级检索  
     

依前列醇多样的信号选择
引用本文:Wise H. 依前列醇多样的信号选择[J]. Acta pharmacologica Sinica, 2003, 24(7): 625-630,724
作者姓名:Wise H
作者单位:DepartmentofPharmacology,FacultyofMedicine,TheChineseUniversityofHongKong,Shatin,NewTerritories,HongKongSAR,China
摘    要:The fate of a cell following stimulation by the prostanoid prostacyclin is cell specific, depending not only on the ability of prostacyclin to activate the cell surface prostacyclin (IP) receptor and regulate its coupling to various G proteins, but also on its ability to act intracellularly via the nuclear peroxisome proliferator-activated receptor family (PPAR). This review will highlight the different signalling options available to prostacyclin, and discuss the consequences for cell responses.

关 键 词:依前列醇 信号选择 环前列腺素 核过氧化酶 环氧合酶 细胞因子

Multiple signalling options for prostacyclin
Wise Helen. Multiple signalling options for prostacyclin[J]. Acta pharmacologica Sinica, 2003, 24(7): 625-630,724
Authors:Wise Helen
Affiliation:Department of Pharmacology, Faculty of Medicine, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong SAR, China. helenwise@cuhk.edu.hk
Abstract:The fate of a cell following stimulation by the prostanoid prostacyclin is cell specific, depending not only on the ability of prostacyclin to activate the cell surface prostacyclin(IP) receptor and regulate its coupling to various G proteins, but also on its ability to act intracellularly via the nuclear peroxisome proliferator-activated receptor family(PPAR). This review will highlight the different signalling options available to prostacyclin, and discuss the consequences for cell responses.
Keywords:epoprostenol  IP receptors  peroxisome proliferator-activated receptors  receptor switching
本文献已被 CNKI 维普 PubMed 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号