颗粒细胞分化的旁分泌机制

Aaron J.W. Hsueh
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引用次数: 38

摘要

由于卵巢中单个卵泡的异质发育不能通过循环促性腺激素水平的变化来解释,因此局部调节因子在旁分泌控制卵泡发育中起重要作用。卵巢类固醇的重要旁分泌作用已被证实。雌激素在增强促性腺激素作用中起重要作用。局部高浓度的雌激素增强促性腺激素对芳香化酶活性的刺激,导致雌激素产生进一步增加。卵泡液中升高的局部雌激素也能增强促黄体生成素受体的促卵泡刺激素诱导。与雌激素类似,局部高浓度孕酮可增强促性腺激素刺激颗粒和黄体细胞中孕酮的生物合成。这种积极的自反馈机制被认为对黄体细胞类固醇生成的自主性很重要。雄激素对卵巢的作用是多种多样的。在缺乏卵泡刺激素的情况下,雄激素主要在卵泡水平上产生负面作用,引起闭锁和颗粒细胞死亡,而在有卵泡刺激素的情况下,雄激素增强卵泡刺激素对黄体酮和雌激素生物合成的刺激。由于雄激素和雌激素似乎相互对抗,这两种类固醇的比例对决定单个卵泡的命运很重要。与卵巢类固醇相比,卵巢肽作为旁分泌信号的作用不太清楚。体外研究清楚地表明,GnRH对卵泡功能具有刺激和抑制作用,而IGF-I和VIP则刺激卵巢类固醇生成。这些肽的作用可能是通过已初步确定的特定颗粒细胞受体介导的。推测GnRH和IGF-I可能由卵巢细胞产生,而VIP可能来源于卵巢神经。预计将开发新的方法来研究单个卵泡作为独立的单位,能够合成、释放激素,并发挥局部旁分泌功能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
6 Paracrine mechanisms involved in granulosa cell differentiation

Since the heterogeneous development of individual follicles in a given ovary cannot be accounted for by changes in circulating gonadotropin levels, local modulatory factors play an important role in the paracrine control of follicular development. The important paracrine role of ovarian steroids has been well established. Oestrogen is important in the augmentation of gonadotropin action. High local concentration of oestrogens enhances the gonadotropin stimulation of aromatase activity, resulting in further increases in oestrogen production. The elevated local oestrogens in the follicular fluid are also capable of enhancing the FSH induction of LH receptors. Similar to oestrogens, local high concentrations of progesterone may enhance the gonadotropin stimulation of progesterone biosynthesis in granulosa and luteal cells. This positive autofeedback mechanism is believed to be important for the autonomy of luteal cell steroidogenesis. Ovarian actions of androgens are diverse. In the absence of FSH, androgens exert mainly negative effects at the follicular level by causing atresia and granulosa cell death, whereas in the presence of FSH, androgens augment FSH stimulation of progesterone and oestrogen biosynthesis. Since androgen and oestrogen appear to antagonize each other's actions, the ratio of these two steroids is important in determining the fate of an individual follicle.

In contrast to ovarian steroids, the role of ovarian peptides as paracrine signals is less clear. In vitro studies clearly demonstrated that GnRH exerts both stimulatory and inhibitory actions on follicular functions, while IGF-I and VIP stimulate ovarian steroidogenesis. The actions of these peptides are presumably mediated through specific granulosa cell receptors that have been tentatively identified. It is presumed that GnRH and IGF-I may be produced by ovarian cells, while VIP may be derived from ovarian nerves. It is anticipated that new methodologies will be developed to study individual follicles as independent units, capable of synthesizing hormones, releasing them, and exerting local paracrine functions.

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