Prostaglandin E receptors

被引:941
作者
Sugimoto, Yukihiko
Narumiya, Shuh [1 ]
机构
[1] Kyoto Univ, Fac Med, Dept Pharmacol, Kyoto 6068501, Japan
[2] Kyoto Univ, Dept Physiol Chem, Grad Sch Pharmaceut Sci, Kyoto 6068501, Japan
关键词
D O I
10.1074/jbc.R600038200
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
Prostaglandin ( PG) E-2 exerts its actions by acting on a group of G-protein-coupled receptors ( GPCRs). There are four GPCRs responding to PGE(2) designated subtypes EP1, EP2, EP3, and EP4 and multiple splicing isoforms of the subtype EP3. The EP subtypes exhibit differences in signal transduction, tissue localization, and regulation of expression. This molecular and biochemical heterogeneity of PGE receptors leads to PGE(2) being the most versatile prostanoid. Studies on knock-out mice deficient in each EP subtype have defined PGE(2) actions mediated by each subtype and identified the role each EP subtype plays in various physiological and pathophysiological responses. Here we review recent advances in PGE receptor research.
引用
收藏
页码:11613 / 11617
页数:5
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