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促卵泡激素诱导颗粒细胞分化时卵泡液刺激因子的特性分析

Characterization of follicular fluid stimulatory factor upon FSH-induced granulosa cell differentiation.

作者信息

Bar-Ami S, Channing C P

机构信息

Department of Physiology, University of Maryland School of Medicine, Baltimore 21201.

出版信息

J Endocrinol Invest. 1988 Dec;11(11):777-83. doi: 10.1007/BF03350222.

Abstract

The modulatory role of follicular fluid (FF) upon gonadotropin-induced granulosa cell (GC) differentiation has been previously demonstrated. In the present study, the stimulatory factor of large-antral FF (LFF) was partially characterized. Addition of ovine FSH to porcine GC culture increased 125I-hCG specific binding about 6-fold and progesterone (P4) secretion 15-fold. The FSH-induced 125I-hCG specific binding was increased 1.9-fold by LFF and decreased 7.7-fold in the presence of small-antral FF (SFF). It is suggested that SFF may contain an inhibitory factor which is overcome by a stimulatory factor accumulated in FF with follicular growth. An initial purification of LFF stimulatory factor was achieved by two-step ethanol elution. The obtained LFF purified fraction increased the FSH-induced 125I-hCG specific binding 1.5-fold and P4 secretion 4.3-fold compared to GC cultured with FSH + LFF. Addition of LH alone increased the P4 secretion 2.3-, 3.4-, and 6 fold in GC precultured with FSH alone, FSH + neat LFF, and FSH + LFF purified fraction, respectively, as compared to GC precultured in plain medium. Therefore, the LFF stimulatory increase of 125I-hCG specific binding may represent an increase of functional LH receptors. Freezing and thawing of LFF 4 times, exposing LFF to urea for 24 h, heating at 60 C for 20 min, and tryptic digestion each abolished the LFF stimulatory effect upon the FSH-dependent increase of 125I-hCG specific binding and P4 secretion. Thus, the LFF stimulatory activity could be attributed to one or more proteins.

摘要

卵泡液(FF)对促性腺激素诱导的颗粒细胞(GC)分化的调节作用先前已得到证实。在本研究中,对大腔卵泡液(LFF)的刺激因子进行了部分特性分析。向猪颗粒细胞培养物中添加绵羊促卵泡激素(FSH)可使¹²⁵I-人绒毛膜促性腺激素(hCG)特异性结合增加约6倍,孕酮(P4)分泌增加15倍。LFF使FSH诱导的¹²⁵I-hCG特异性结合增加1.9倍,而在小腔卵泡液(SFF)存在时则降低7.7倍。提示SFF可能含有一种抑制因子,而随着卵泡生长在卵泡液中积累的刺激因子可克服该抑制因子。通过两步乙醇洗脱实现了LFF刺激因子的初步纯化。与用FSH + LFF培养的颗粒细胞相比,获得的LFF纯化组分使FSH诱导的¹²⁵I-hCG特异性结合增加1.5倍,P4分泌增加4.3倍。与在普通培养基中预培养的颗粒细胞相比,单独添加促黄体生成素(LH)分别使在单独用FSH、FSH + 纯LFF和FSH + LFF纯化组分预培养的颗粒细胞中的P4分泌增加2.3倍、3.4倍和6倍。因此,LFF对¹²⁵I-hCG特异性结合的刺激增加可能代表功能性LH受体的增加。LFF冻融4次、在尿素中暴露24小时、在60℃加热20分钟以及胰蛋白酶消化均消除了LFF对FSH依赖性¹²⁵I-hCG特异性结合增加和P4分泌的刺激作用。因此,LFF的刺激活性可能归因于一种或多种蛋白质。

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