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促性腺激素、激活素、TGF-β 和 BMP-15 对斑马鱼卵巢中膜孕激素受体的调节。

Regulation of membrane progestin receptors in the zebrafish ovary by gonadotropin, activin, TGF-beta and BMP-15.

机构信息

Department of Biology, York University, 4700 Keele Street, Toronto, Ontario M3J 1P3, Canada.

出版信息

Mol Cell Endocrinol. 2009 Nov 27;312(1-2):72-9. doi: 10.1016/j.mce.2009.03.011. Epub 2009 Mar 28.

Abstract

Progestin hormones are vital for inducing oocyte maturation in fish by binding to membrane progestin receptors (mPRs). The aim of this study was to examine the expression and regulation of mPRalpha and mPRbeta in zebrafish follicles. First, defolliculated fully grown oocytes were subjected to immunofluorescent staining using anti-mPRalpha and mPRbeta antibodies, and their expression on the oocyte membrane was confirmed. Second, total protein was collected from zebrafish follicles and Western blotting revealed that the level of mPRalpha and mPRbeta increased with follicle development. We have previously shown that several members of the transforming growth factor-beta (TGF-beta) superfamily, including TGF-beta1, activin-A, and bone morphogenetic protein (BMP)-15, regulate oocyte maturation in zebrafish. Therefore, the third major focus of this study was to test if these growth factors, as well as gonadotropins, regulate the expression of mPRs. Overexpression of BMP-15 significantly reduced, while knockdown of BMP-15 increased, mPRbeta levels. However, mPRalpha expression level remained unchanged with BMP-15 overexpression or knockdown. Treatment of follicles with human chorionic gonadotropin (hCG) resulted in an increased in mPRbeta, but not mPRalpha, expression levels. Activin-A induced the expression of mPRalpha and mPRbeta in a dose- and time-dependent manner. On the other hand, TGF-beta1 treatment suppressed the expression of mPRbeta, but not mPRalpha. Taken together, these findings further support the role of mPRs in oocyte maturation and suggest that gonadotropins, BMP-15, activin-A, and TGF-beta1 exert their regulatory effects on oocyte maturation in part by regulating mPR expression.

摘要

孕激素通过与膜孕激素受体(mPR)结合对鱼类卵母细胞成熟至关重要。本研究旨在研究斑马鱼滤泡中 mPRalpha 和 mPRbeta 的表达和调节。首先,用抗 mPRalpha 和 mPRbeta 抗体对去滤泡完全生长的卵母细胞进行免疫荧光染色,证实其在卵母细胞膜上的表达。其次,从斑马鱼滤泡中提取总蛋白,Western blot 显示 mPRalpha 和 mPRbeta 的水平随滤泡发育而增加。我们之前已经表明,转化生长因子-β(TGF-β)超家族的几个成员,包括 TGF-β1、激活素-A 和骨形态发生蛋白(BMP)-15,调节斑马鱼卵母细胞成熟。因此,本研究的第三个重点是测试这些生长因子以及促性腺激素是否调节 mPR 的表达。BMP-15 的过表达显著降低,而 BMP-15 的敲低增加了 mPRbeta 的水平。然而,BMP-15 的过表达或敲低对 mPRalpha 的表达水平没有影响。用人绒毛膜促性腺激素(hCG)处理滤泡导致 mPRbeta 的表达增加,但 mPRalpha 的表达水平不变。激活素-A 以剂量和时间依赖的方式诱导 mPRalpha 和 mPRbeta 的表达。另一方面,TGF-β1 处理抑制了 mPRbeta 的表达,但不抑制 mPRalpha。总之,这些发现进一步支持了 mPR 在卵母细胞成熟中的作用,并表明促性腺激素、BMP-15、激活素-A 和 TGF-β1 通过调节 mPR 表达对卵母细胞成熟发挥其调节作用。

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