Roberts A J, Skinner M K
Department of Pharmacology, Vanderbilt University School of Medicine, Nashville, Tennessee 37232-6600.
Endocrinology. 1991 Oct;129(4):2041-8. doi: 10.1210/endo-129-4-2041.
The actions and interactions of transforming growth factor-alpha (TGF alpha) and TGF beta on growth and differentiation of bovine thecal cells were investigated. Bovine thecal interna cells were isolated from small (less than 5 mm), medium (5-10 mm), and large (greater than 10 mm) antral follicles and cultured in the presence or absence of TGF alpha and/or TGF beta. Both [3H]thymidine incorporation and changes in cell number (i.e. DNA levels) were evaluated to determine effects on thecal cell growth. Short term treatment of cells with TGF alpha (18-24 h) stimulated thymidine incorporation, and longer term treatments (4 days) increased cell number. TGF beta suppressed thymidine incorporation below that observed in untreated cultures, but had no effect on cell number. When combined with TGF alpha, TGF beta suppressed the ability of TGF alpha to stimulate thymidine incorporation and increase cell number. The response to these growth factors was similar for cells isolated from the different stages of antral follicle development. The effects of TGF alpha and TGF beta on thecal cell differentiation were evaluated by quantitating changes in androstenedione and progesterone accumulation in cultures treated with TGFs in the absence (basal) or presence of hCG, estradiol (E2), or a combination of hCG and E2. E2 and hCG were included in this study because previous research has demonstrated that these hormones alter thecal cell steroidogenesis. Treatment with TGF alpha resulted in a suppression of basal and hormonally stimulated accumulation of androstenedione during days 0-3 of culture, whereas TGF beta did not significantly alter androstenedione accumulation. TGF alpha also suppressed progesterone accumulation during days 0-3 of culture in the absence or presence of hormones. In contrast, TGF beta stimulated accumulation of progesterone in cultures that did not contain E2, which suppressed progesterone during this period. Therefore, during days 0-3 of culture, TGF alpha appears to have suppressive effects on androstenedione and progesterone production, whereas TGF beta can stimulate progesterone production in the absence of E2. During days 3-6 of culture, thecal cell differentiation changes, and the capacity to produce androstenedione dramatically declines, while the capacity to produce progesterone increases. During this period, either TGF alpha or TGF beta slightly increased basal progesterone accumulation and partially suppressed the ability of hCG to stimulate progesterone. The effects of TGFs on thecal cell steroidogenesis were similar with cells isolated from the different stages of antral follicle development. Results from these studies provide evidence that THF alpha and TGF beta can modulate thecal cell growth and differentiation (i.e. steroidogenesis).(ABSTRACT TRUNCATED AT 400 WORDS)
研究了转化生长因子α(TGFα)和TGFβ对牛卵泡膜细胞生长和分化的作用及相互作用。从直径小于5毫米的小卵泡、5 - 10毫米的中卵泡和大于10毫米的大卵泡中分离牛卵泡膜内层细胞,并在有或无TGFα和/或TGFβ的情况下进行培养。通过评估[3H]胸苷掺入和细胞数量变化(即DNA水平)来确定对卵泡膜细胞生长的影响。用TGFα对细胞进行短期处理(18 - 24小时)可刺激胸苷掺入,长期处理(4天)则可增加细胞数量。TGFβ可将胸苷掺入抑制至未处理培养物以下水平,但对细胞数量无影响。当与TGFα联合使用时,TGFβ可抑制TGFα刺激胸苷掺入和增加细胞数量的能力。从不同发育阶段的卵泡中分离的细胞对这些生长因子的反应相似。通过定量在无(基础)或有hCG、雌二醇(E2)或hCG与E2组合存在的情况下用TGFs处理的培养物中雄烯二酮和孕酮积累的变化,评估TGFα和TGFβ对卵泡膜细胞分化的影响。本研究纳入E2和hCG是因为先前的研究表明这些激素会改变卵泡膜细胞的类固醇生成。用TGFα处理导致培养第0 - 3天基础和激素刺激的雄烯二酮积累受到抑制,而TGFβ并未显著改变雄烯二酮积累。在培养第0 - 3天,无论有无激素,TGFα也抑制孕酮积累。相反,TGFβ可刺激不含E2的培养物中孕酮的积累,而E2在此期间会抑制孕酮积累。因此,在培养第0 - 3天,TGFα似乎对雄烯二酮和孕酮产生具有抑制作用,而TGFβ在无E2时可刺激孕酮产生。在培养第3 - 6天,卵泡膜细胞分化发生变化,产生雄烯二酮的能力显著下降,而产生孕酮的能力增加。在此期间,TGFα或TGFβ均可轻微增加基础孕酮积累,并部分抑制hCG刺激孕酮的能力。从不同发育阶段的卵泡中分离的细胞对TGFs对卵泡膜细胞类固醇生成的影响相似。这些研究结果提供了证据,表明TGFα和TGFβ可调节卵泡膜细胞的生长和分化(即类固醇生成)。(摘要截选至400字)