Knight P G, Glister C
School of Animal and Microbial Sciences, The University of Reading, Whiteknights, Reading RG6 6AJ, UK.
Reproduction. 2001 Apr;121(4):503-12. doi: 10.1530/rep.0.1210503.
The changing pattern of granulosa cell expression of inhibin/activin subunits and follistatin during follicle development and their differential regulation by extrinsic and intraovarian factors supports evidence from functional studies, mostly in vitro, that these proteins have important roles in folliculogenesis, oocyte maturation and corpus luteum function. Gonadal inhibins function as negative feedback hormones to regulate the synthesis and secretion of pituitary FSH, a key determinant of follicle development, but there is little supportive evidence for a peripheral endocrine role for ovary-derived activins or follistatin in this regard. However, activins and follistatin are expressed in numerous other tissues, including anterior pituitary, and they are firmly implicated as local intrapituitary regulators of FSH secretion. Intraovarian actions of granulosa cell-derived activins include the promotion of granulosa cell proliferation and upregulation of FSH receptors, P450arom, oestrogen synthesis, granulosa cell LH receptors and enhancement of oocyte maturation. Through its activin-binding role, follistatin can reverse each of these activin-induced responses. In addition to their endocrine feedback role, granulosa-derived inhibins can sensitize theca cells to LH, thereby enhancing the production of androgens, an essential requirement for follicular oestrogen synthesis. Activins can oppose this effect and suppress thecal androgen production. Granulosa cells overproduce inhibin a subunit precursor relative to betaA/betaB subunit precursors and evidence indicates that different parts of the inhibin a subunit precursor have intrinsic biological activities distinct from inhibin alphabetaA/B dimer, and serve as additional local modulators of follicle and corpus luteum function.
在卵泡发育过程中,抑制素/激活素亚基和卵泡抑素在颗粒细胞中的表达模式不断变化,且它们受到外在因素和卵巢内因素的差异调节,这支持了大多来自体外功能研究的证据,即这些蛋白质在卵泡发生、卵母细胞成熟和黄体功能中发挥重要作用。性腺抑制素作为负反馈激素,调节垂体促卵泡激素(FSH)的合成与分泌,而FSH是卵泡发育的关键决定因素,但在这方面,几乎没有支持卵巢来源的激活素或卵泡抑素具有外周内分泌作用的证据。然而,激活素和卵泡抑素在包括垂体前叶在内的许多其他组织中表达,并且它们被确认为垂体FSH分泌的局部调节因子。颗粒细胞来源的激活素在卵巢内的作用包括促进颗粒细胞增殖、上调FSH受体、P450芳香化酶、雌激素合成、颗粒细胞LH受体以及增强卵母细胞成熟。通过其与激活素结合的作用,卵泡抑素可以逆转这些激活素诱导的每一种反应。除了其内分泌反馈作用外,颗粒细胞来源的抑制素可以使卵泡膜细胞对LH敏感,从而增强雄激素的产生,而雄激素是卵泡雌激素合成的必要条件。激活素可以对抗这种作用并抑制卵泡膜细胞雄激素的产生。相对于βA/βB亚基前体,颗粒细胞过度产生抑制素α亚基前体,并且有证据表明抑制素α亚基前体的不同部分具有与抑制素αβA/B二聚体不同的内在生物学活性,并作为卵泡和黄体功能的额外局部调节因子。