Laboratory of Reproductive and Developmental Biology, Hokkaido University, Sapporo 060-0810, Japan.
Mol Cell Endocrinol. 2012 Oct 15;362(1-2):76-84. doi: 10.1016/j.mce.2012.05.013. Epub 2012 Jun 1.
A cDNA for a prostaglandin E(2) (PGE(2)) receptor subtype 4, EP4b (Ptger4b), was cloned from the medaka ovary. The effect of PGE(2) was examined using COS-7 cells expressing the recombinant Ptger4b protein. An increase in intracellular cAMP levels was observed when the cells were incubated with PGE(2), but the increase in cAMP levels was nullified by the addition of the EP4 antagonist GW627368X. The expression of ptger4b mRNA was drastically induced by the addition of pregnant mare serum gonadotropin to the in vitro culture of large preovulatory follicles. In in vitro ovulation studies of the effect of GW627368X addition on follicle ovulation, the critical timing of the PGE(2)/Ptger4b interaction was suggested to be between -1 and 0 h of ovulation. These results further substantiate that PGE(2)/Ptger4b signaling is involved in follicle rupture during ovulation in the medaka ovary.
从牙鲆卵巢中克隆出一种前列腺素 E(2) (PGE(2))受体亚型 4,即 EP4b (Ptger4b) 的 cDNA。使用表达重组 Ptger4b 蛋白的 COS-7 细胞检测 PGE(2)的作用。当细胞孵育 PGE(2)时,观察到细胞内 cAMP 水平增加,但添加 EP4 拮抗剂 GW627368X 后,cAMP 水平的增加被消除。在大腔前卵泡的体外培养中加入孕马血清促性腺激素,ptger4b mRNA 的表达明显增加。在 GW627368X 添加对卵泡排卵作用的体外排卵研究中,提示 PGE(2)/Ptger4b 相互作用的关键时间是排卵前-1 至 0 小时。这些结果进一步证实 PGE(2)/Ptger4b 信号参与了牙鲆卵巢排卵期间的卵泡破裂。