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Signal Transduction for FSH Regulating Ovarian Differentiation

机译:FSH调节卵巢分化的信号转导

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摘要

The paper gives a brief summary of our work related to signal transduction of FSH-regulated follicular differentiation and function. The review mainly concentrated in the three aspects: (1) Regulation of stem cell factor (SCF) in the primordial follicles and its signal transduction; (2) Role of ERK1/2 in FSH-regulated proliferative activity and steroidogenesis in granulosa cells (GC); (3) FSH receptor activation of p38 MAPK and steroidogenesis in GC. We have demonstrated in these studies that (1) SCF prevents oocyte from apoptosis in the cultured ovaries. Addition of a SCF specific inhibitor, PI3K, abolishes the anti-apoptotic action of SCF; (2) FSH promotes PCNA expression, and increases the cell ability of steroidogenesis in the cultured primary GCs, suggesting that the activated ERK1/2 may be involved in the regulation of FSH in GC proliferation and differentiation; (3) FSH-activated p38 MAPK pathway regulates progesterone and estrogen synthesis in GCs differently, LRH-1 and DAX-1 may be the effective transcription factor in the signal transduction.
机译:本文简要概述了我们与FSH调节的卵泡分化和功能的信号转导有关的工作。综述主要集中在三个方面:(1)原始卵泡中干细胞因子(SCF)的调控及其信号转导; (2)ERK1 / 2在FSH调节的颗粒细胞(GC)增殖活性和类固醇生成中的作用; (3)GC中FSH受体激活p38 MAPK和类固醇生成。在这些研究中我们已经证明(1)SCF阻止卵母细胞在培养的卵巢中凋亡。加入SCF特异性抑制剂PI3K消除了SCF的抗凋亡作用; (2)FSH促进了PCNA的表达,并提高了原代培养的GC中类固醇生成的细胞能力,提示活化的ERK1 / 2可能参与了FSH在GC增殖和分化中的调控。 (3)FSH激活的p38 MAPK途径对GC中的孕酮和雌激素合成有不同的调节作用,LRH-1和DAX-1可能是信号转导的有效转录因子。

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