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大鼠卵巢培养颗粒细胞分化和凋亡过程中血管紧张素II 2型受体的特征分析

Characterization of angiotensin II receptor type 2 during differentiation and apoptosis of rat ovarian cultured granulosa cells.

作者信息

Tanaka M, Ohnishi J, Ozawa Y, Sugimoto M, Usuki S, Naruse M, Murakami K, Miyazaki H

机构信息

Institute of Applied Biochemistry, University of Tsukuba, Ibaraki, Japan.

出版信息

Biochem Biophys Res Commun. 1995 Feb 15;207(2):593-8. doi: 10.1006/bbrc.1995.1229.

Abstract

We examined the change in the content of angiotensin II (AII) receptor type 2 (AT2) during differentiation and apoptosis of rat ovarian granulosa cells in culture. The AT2 content was not changed by follicle stimulating hormone (FSH), a differentiation factor of granulosa cells, but was markedly increased in FSH-free media. The cells cultured without FSH underwent internucleosomal DNA fragmentation characteristic of apoptosis, which occurs during follicle atresia. AII augmented the increase in the AT2 content in the absence of FSH. This AII-induced augmentation was suppressed by the AT2-selective antagonist PD123319 but not by Dup753, an antagonist specific for type 1 receptor, suggesting that AII up-regulates the AT2 expression via AT2 itself. These data strongly support the hypothesis that AT2 might modulate the onset and progression of follicle atresia involving apoptosis of granulosa cells.

摘要

我们研究了培养的大鼠卵巢颗粒细胞在分化和凋亡过程中血管紧张素II(AII)2型受体(AT2)含量的变化。颗粒细胞的分化因子促卵泡激素(FSH)不会改变AT2的含量,但在无FSH的培养基中其含量会显著增加。在无FSH条件下培养的细胞发生了凋亡特有的核小体间DNA片段化,这种凋亡发生在卵泡闭锁过程中。在无FSH的情况下,AII增强了AT2含量的增加。AT2选择性拮抗剂PD123319可抑制这种AII诱导的增强作用,但1型受体特异性拮抗剂Dup753则无此作用,这表明AII通过AT2自身上调AT2的表达。这些数据有力地支持了以下假说:AT2可能通过颗粒细胞凋亡调节卵泡闭锁的发生和进展。

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