Biological roles of angiotensin II via its type 2 receptor during rat follicle atresia

被引:35
作者
Kotani, E
Sugimoto, M
Kamata, H
Fujii, N
Saitoh, M
Usuki, S
Kubo, T
Song, KF
Miyazaki, M
Murakami, K
Miyazaki, H [1 ]
机构
[1] Univ Tsukuba, Gene Expt Ctr, Inst Appl Biochem, Tsukuba, Ibaraki 3058572, Japan
[2] Univ Tsukuba, Inst Clin Med, Dept Obstet & Gynecol, Tsukuba, Ibaraki 3058572, Japan
[3] Osaka Med Coll, Dept Pharmacol, Takatsuki, Osaka 569, Japan
来源
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM | 1999年 / 276卷 / 01期
关键词
ovarian renin-angiotensin system; follicle-stimulating hormone; luteinizing hormone receptor; estrogen; polycystic ovary syndrome;
D O I
10.1152/ajpendo.1999.276.1.E25
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Type I angiotensin II (ANG II) receptors play crucial roles in the regulation of blood pressure and fluid osmolarity, whereas the physiological roles of type 2 ANG II receptors (AT(2)) remain unclear. Because AT2 is expressed in atretic follicles where granulosa cells undergo apoptosis, we examined the space and time relationship between AT2 expression and follicle atresia in vivo and the effect of AT(2) on follicle-stimulating hormone (FSH) actions in vitro. Binding studies, autoradiography, and RT-PCR of AT(2) revealed that the AT2 content in granulosa cells was time dependently increased at both protein and mRNA levels in equine chorionic gonadotropin-treated immature female rats. This increase paralleled the progression of atresia. ANG II suppressed FSH-caused prevention of DNA fragmentation, increases in luteinizing hormone receptor content, and estrogen production through AT2 in cultured granulosa cells. Moreover, FSH-induced stimulation of extracellular signal-regulated kinase activity, critical for cell survival, was inhibited by AT2 stimulation. These results suggest that AT2 mediates the progression of follicle atresia through granulosa cell. apoptosis by inhibiting FSH actions.
引用
收藏
页码:E25 / E33
页数:9
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