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滤泡期抑制素通过调节颗粒细胞凋亡和类固醇生成。

Follicular stage-dependent regulation of apoptosis and steroidogenesis by prohibitin in rat granulosa cells.

机构信息

Department of Cellular & Molecular Medicine, University of Ottawa, Ottawa, Ontario, K1H 8L6Canada.

出版信息

J Ovarian Res. 2013 Apr 8;6(1):23. doi: 10.1186/1757-2215-6-23.

Abstract

BACKGROUND

Follicular growth and atresia are tightly regulated processes, which involve the participation of endocrine, autocrine and paracrine factors at the cellular level. Prohibitin (PHB) is a multifunctional intracellular protein playing an important role in the regulation of proliferation, apoptosis and differentiation. Here we examined the expression of PHB and its regulation by FSH in vitro and studied the role of PHB in the regulation of apoptosis and steroidogenesis in response to the apoptosis inducer staurosporine (STS) and to FSH, respectively.

METHODS

Undifferentiated and differentiated granulosa cells were collected from diethylstilbestrol (DES)- and equine chronic gonadotropin (eCG)-primed immature rats, respectively and then cultured with various treatments (FSH, adenovirus infection, STS) according to experimental design. The apoptosis rate, the production of estradiol and progesterone, and the expression of distinct proteins (PHB, caspase-3, phospho- and total Akt) were assessed.

RESULTS

PHB is anti-apoptotic and its action is dependent on the differentiated state of the granulosa cells. Data from gain- and loss-of-function experiments demonstrate that PHB inhibited STS-induced caspase-3 cleavage and apoptosis in undifferentiated granulosa cells, but was ineffective in differentiated cells. In contrast, PHB suppresses FSH-induced steroidogenesis and this response is evident irrespective of the differentiated state of granulosa cells.

CONCLUSION

These findings suggest that PHB regulates granulosa cell apoptosis and steroidogenesis in a follicular stage-dependent manner and that the dysregulation of PHB expression and action may be relevant to ovarian dysfunction.

摘要

背景

卵泡的生长和闭锁是一个受到严格调控的过程,涉及到细胞水平上内分泌、自分泌和旁分泌因子的参与。抑制素(PHB)是一种多功能的细胞内蛋白,在调节增殖、凋亡和分化方面发挥着重要作用。在这里,我们研究了 PHB 的表达及其在外源性 FSH 作用下的调节,并分别研究了 PHB 在凋亡诱导剂 staurosporine(STS)和 FSH 作用下对凋亡和类固醇生成的调节作用。

方法

分别从己烯雌酚(DES)和马促性腺激素(eCG)诱导的未成熟大鼠中收集未分化和分化的颗粒细胞,并根据实验设计用不同的处理方法(FSH、腺病毒感染、STS)进行培养。评估细胞凋亡率、雌二醇和孕酮的产生以及不同蛋白(PHB、caspase-3、磷酸化和总 Akt)的表达。

结果

PHB 具有抗凋亡作用,其作用依赖于颗粒细胞的分化状态。功能获得和功能丧失实验的数据表明,PHB 抑制了未分化颗粒细胞中 STS 诱导的 caspase-3 切割和凋亡,但在分化细胞中无效。相反,PHB 抑制了 FSH 诱导的类固醇生成,而这一反应与颗粒细胞的分化状态无关。

结论

这些发现表明,PHB 以卵泡期依赖性的方式调节颗粒细胞凋亡和类固醇生成,PHB 表达和功能的失调可能与卵巢功能障碍有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/665b/3635931/897f495a9794/1757-2215-6-23-1.jpg

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