Molecular cloning and expression of a rat prostaglandin E2 receptor of the EP2 subtype

被引:65
作者
Nemoto, K
Pilbeam, CC
Bilak, SR
Raisz, LG [1 ]
机构
[1] Univ Connecticut, Ctr Hlth, Dept Med, Div Endocrinol & Metab, Farmington, CT 06030 USA
[2] Univ Connecticut, Ctr Hlth, Dept Anat, Farmington, CT 06030 USA
[3] Univ Connecticut, Ctr Hlth, Ctr Neurol Sci, Farmington, CT 06030 USA
来源
PROSTAGLANDINS & OTHER LIPID MEDIATORS | 1997年 / 54卷 / 04期
关键词
prostaglandin E2 receptor; EP2;
D O I
10.1016/S0090-6980(97)00145-7
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 E-2 (PGE(2)) is a potent local mediator of cell growth and differentiation in various tissues. The receptors for PGE(2) have been classified into four pharmacological subtypes, EP1, EP2, EP3, and EP4, based on the responses to selective agonists and antagonists. We have cloned a functional cDNA for the rat EP2 receptor subtype from a rat lung cDNA library. The rat EP2 receptor cDNA encodes 357 amino acid residues having high homology with the human and mouse EP2 receptors and containing seven putative transmembrane domains. In COS-7 cells transfected with rat EP2 cDNA, specific [H-3]PGE(2) binding was found with a dissociation constant of 14.9 nM, and this binding was inhibited by unlabeled PGE(2) and PGF(2 alpha). PGE(2) and butaprost, an EP2 selective agonist, were effective in increasing the cAMP level in the COS-7 cell transfectants. Northern blot and RT-PCR analysis showed widespread distribution of the EP2 receptor in various tissues. Higher EP2 expression was found in fetal long bones and calvariae than in adult by RT-PCR and in situ hybridization, suggesting a role for this receptor in rapidly growing skeletal tissue.
引用
收藏
页码:713 / 725
页数:13
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