Hansel W, Alila H W, Dowd J P, Milvae R A
Department of Physiology, Cornell University, Ithaca, NY 14853.
J Reprod Fertil Suppl. 1991;43:77-89.
Studies of the calcium requirement and the relationship of intracellular calcium to progesterone synthesis in highly purified preparations of bovine luteal cells reveal a remarkably close relationship between intracellular calcium levels and steroidogenesis. The differential responses of the two cell types, summarized in Table 2, are beginning to reveal how the two cell types may co-operate to produce both luteotrophic and luteolytic responses at different stages of the oestrous cycle and early pregnancy. The luteotrophic mechanisms in the small cells are fairly clear; in addition to the luteotrophic effects of LH and cAMP, activation of protein kinase C leads to increased progesterone synthesis. Accordingly, PGF-2 alpha and several other prostanoids are luteotrophic in these cells. PGF-2 alpha stimulates phospholipase C activity in the small cells but does not reduce LH-stimulated cAMP or progesterone accumulation (Davis et al., 1989). This acute stimulus of protein kinase C activation to progesterone production in bovine small luteal cells is rapidly desensitized, although its stimulus to prostanoid production continues for at least 24 h. Large cells respond to LH, but only at relatively high levels. In addition, we have no good evidence for a role for protein kinase C in the control of progesterone synthesis in the large bovine luteal cells from mid-cycle corpora lutea. Phorbol esters have no effect on steroidogenesis and it is not yet established that protein kinase C provides the same high affinity receptor for phorbol esters that is found in the small cells. Experiments with inhibitors of protein kinase C, such as staurosporine, in large cells have been inconclusive. Evidence for several species suggests that both cell types co-operate, in ways not yet fully understood, to bring about maximal progesterone production at mid-cycle. Some evidence suggests that they may also co-operate to bring about luteolysis. The concept that PGF-2 alpha initiates luteolysis by inhibiting LH stimulated progesterone production in the large cells must be revised in light of the relative insensitivity of these cells to LH and the fact that they probably constitutively express the cholesterol side-chain cleavage enzymes (P-450scc) that represent the rate-limiting step in progesterone production. Oonk et al. (1989) have reported that, once P-450scc mRNA is induced in rat granulosa cells by the LH surge, it is constitutively maintained by the luteinized cells in the absence of gonadotrophins and is no longer regulated by cAMP.(ABSTRACT TRUNCATED AT 400 WORDS)
对高度纯化的牛黄体细胞制剂中钙需求以及细胞内钙与孕酮合成关系的研究表明,细胞内钙水平与类固醇生成之间存在着显著的紧密关系。表2总结了两种细胞类型的不同反应,这开始揭示出在发情周期和妊娠早期的不同阶段,这两种细胞类型可能如何协同作用以产生促黄体生成和黄体溶解反应。小细胞中的促黄体生成机制相当明确;除了促黄体生成素(LH)和环磷酸腺苷(cAMP)的促黄体生成作用外,蛋白激酶C的激活会导致孕酮合成增加。因此,前列腺素F2α(PGF - 2α)和其他几种前列腺素在这些细胞中具有促黄体生成作用。PGF - 2α刺激小细胞中的磷脂酶C活性,但不会降低LH刺激的cAMP或孕酮积累(戴维斯等人,1989年)。尽管其对前列腺素产生的刺激至少持续24小时,但这种对牛小黄体细胞中蛋白激酶C激活以促进孕酮产生的急性刺激会迅速脱敏。大细胞对LH有反应,但仅在相对较高水平时才有反应。此外,我们没有充分证据表明蛋白激酶C在中期黄体的大的牛黄体细胞中孕酮合成的控制中发挥作用。佛波酯对类固醇生成没有影响,并且尚未确定蛋白激酶C是否像在小细胞中那样为佛波酯提供相同的高亲和力受体。在大细胞中使用蛋白激酶C抑制剂(如星形孢菌素)进行的实验尚无定论。有证据表明,对于几种物种来说,这两种细胞类型以尚未完全理解的方式协同作用,以在周期中期实现最大的孕酮产生。一些证据表明它们也可能协同导致黄体溶解。鉴于这些细胞对LH相对不敏感以及它们可能组成性表达代表孕酮产生限速步骤的胆固醇侧链裂解酶(P - 450scc)这一事实,必须修正PGF - 2α通过抑制大细胞中LH刺激的孕酮产生来启动黄体溶解的概念。翁克等人(1989年)报告说,一旦LH峰在大鼠颗粒细胞中诱导出P - 450scc信使核糖核酸(mRNA),它在不存在促性腺激素的情况下由黄体化细胞组成性维持,并且不再受cAMP调节。(摘要截至于400字)