MOLECULAR MECHANISMS OF DIVERSE ACTIONS OF PROSTANOID RECEPTORS

被引:354
作者
NEGISHI, M [1 ]
SUGIMOTO, Y [1 ]
ICHIKAWA, A [1 ]
机构
[1] KYOTO UNIV,FAC PHARMACEUT SCI,DEPT PHYSIOL CHEM,SAKYO KU,KYOTO 606,JAPAN
来源
BIOCHIMICA ET BIOPHYSICA ACTA-LIPIDS AND LIPID METABOLISM | 1995年 / 1259卷 / 01期
关键词
PROSTANOID; ARACHIDONIC ACID; RHODOPSIN-TYPE RECEPTOR; GTP-BINDING PROTEIN; ALTERNATIVE SPLICING;
D O I
10.1016/0005-2760(95)00146-4
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
This review summarizes recent advances in the molecular characterization of prostanoid receptors. Prostanoids exert versatile actions in diverse tissues and cells through specific cell surface receptors. Molecular biological studies revealed the primary structure of eight types and subtypes of prostanoid receptor from various species. These include the thromboxane A(2) receptor, prostacyclin receptor, prostaglandin (PG) F receptor, PGD receptor and four subtypes of PGE receptors. They are coupled to different signal transduction systems. In addition, multiple isoforms of PGE receptor EP3 subtype have been identified in various species. They are produced through alternative RNA splicing from a single gene and differ only in their carboxy-terminal tails. These isoforms differ in the efficiency of G protein activation, in the specificity of coupling to G proteins or in sensitivity to desensitization. This molecular characterization is useful for understanding the diverse physiological roles of prostanoids.
引用
收藏
页码:109 / 119
页数:11
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