Glister Claire, Groome Nigel P, Knight Philip G
School of Animal and Microbial Sciences, University of Reading, Whiteknights, Reading RG6 6AJ, United Kingdom.
Biol Reprod. 2003 Mar;68(3):758-65. doi: 10.1095/biolreprod.102.008698.
The objective was to investigate the potential role of the oocyte in modulating proliferation and basal, FSH-induced and insulin-like growth factor (IGF)-induced secretion of inhibin A (inh A), activin A (act A), follistatin (FS), estradiol (E(2)), and progesterone (P(4)) by mural bovine granulosa cells. Cells from 4- to 6-mm follicles were cultured in serum-free medium containing insulin and androstenedione, and the effects of ovine FSH and IGF analogue (LR3-IGF-1) were tested alone and in the presence of denuded bovine oocytes (2, 8, or 20 per well). Medium was changed every 48 h, cultures were terminated after 144 h, and viable cell number was determined. Results are based on combined data from four independent cultures and are presented for the last time period only when responses were maximal. Both FSH and IGF increased (P < 0.001) secretion of inh A, act A, FS, E(2), and P(4) and raised cell number. In the absence of FSH or IGF, coculture with oocytes had no effect on any of the measured hormones, although cell number was increased up to 1.8-fold (P < 0.0001). Addition of oocytes to FSH-stimulated cells dose-dependently suppressed (P < 0.0001) inh A (6-fold maximum suppression), act A (5.5-fold), FS (3.6-fold), E(2) (4.6-fold), and P(4) (2.4-fold), with suppression increasing with FSH dose. Likewise, oocytes suppressed (P < 0.001) IGF-induced secretion of inh A, act A, FS, and E(2) (P < 0.05) but enhanced IGF-induced P(4) secretion (1.7-fold; P < 0.05). Given the similarity of these oocyte-mediated actions to those we observed previously following epidermal growth factor (EGF) treatment, we used immunocytochemistry to determine whether bovine oocytes express EGF or transforming growth factor (TGF) alpha. Intense staining with TGFalpha antibody (but not with EGF antibody) was detected in oocytes both before and after coculture. Experiments involving addition of TGFalpha to granulosa cells confirmed that the peptide mimicked the effects of oocytes on cell proliferation and on FSH- and IGF-induced hormone secretion. These experiments indicate that bovine oocytes secrete a factor(s) capable of modulating granulosa cell proliferation and responsiveness to FSH and IGF in terms of steroidogenesis and production of inhibin-related peptides, bovine oocytes express TGFalpha but not EGF, and TGFalpha is a prime candidate for mediating the actions of oocytes on bovine granulosa cells.
目的是研究卵母细胞在调节壁层牛颗粒细胞增殖以及基础状态、促卵泡激素(FSH)诱导和胰岛素样生长因子(IGF)诱导的抑制素A(inh A)、激活素A(act A)、卵泡抑素(FS)、雌二醇(E₂)和孕酮(P₄)分泌方面的潜在作用。将来自4至6毫米卵泡的细胞培养于含有胰岛素和雄烯二酮的无血清培养基中,单独测试绵羊FSH和IGF类似物(LR3-IGF-1)的作用,以及在存在去透明带牛卵母细胞(每孔2个、8个或20个)的情况下测试其作用。每48小时更换一次培养基,144小时后终止培养,并测定活细胞数量。结果基于来自四个独立培养物的合并数据,仅在反应达到最大值的最后一个时间段呈现。FSH和IGF均增加(P < 0.001)inh A、act A、FS、E₂和P₄的分泌并增加细胞数量。在不存在FSH或IGF的情况下,与卵母细胞共培养对任何所测激素均无影响,尽管细胞数量增加了1.8倍(P < 0.0001)。将卵母细胞添加到FSH刺激的细胞中,剂量依赖性地抑制(P < 0.0001)inh A(最大抑制6倍)、act A(5.5倍)、FS(3.6倍)、E₂(4.6倍)和P₄(2.4倍),抑制作用随FSH剂量增加而增强。同样,卵母细胞抑制(P < 0.001)IGF诱导的inh A、act A、FS和E₂分泌(P < 0.05),但增强IGF诱导的P₄分泌(1.7倍;P < 0.05)。鉴于这些卵母细胞介导的作用与我们之前观察到的表皮生长因子(EGF)处理后的作用相似,我们使用免疫细胞化学来确定牛卵母细胞是否表达EGF或转化生长因子(TGF)α。在共培养前后的卵母细胞中均检测到TGFα抗体的强烈染色(但未检测到EGF抗体的染色)。涉及向颗粒细胞添加TGFα的实验证实,该肽模拟了卵母细胞对细胞增殖以及对FSH和IGF诱导的激素分泌的影响。这些实验表明,牛卵母细胞分泌一种能够调节颗粒细胞增殖以及在类固醇生成和抑制素相关肽产生方面对FSH和IGF反应性的因子,牛卵母细胞表达TGFα但不表达EGF,并且TGFα是介导卵母细胞对牛颗粒细胞作用的主要候选因子。