Spicer L J, Aad P Y, Allen D, Mazerbourg S, Hsueh A J
Department of Animal Science, Oklahoma State University, Stillwater, Oklahoma 74078, USA.
J Endocrinol. 2006 May;189(2):329-39. doi: 10.1677/joe.1.06503.
In addition to gonadotropins, steroidogenesis and proliferation of granulosa cells during follicular development are controlled by a number of intraovarian factors including growth differentiation factor-9 (GDF-9), bone morphogenetic protein-4 (BMP-4), and IGF-I. The objective of this study was to determine the effect of GDF-9 and BMP-4 and their interaction with IGF-I and FSH on ovarian granulosa cell function in cattle. Granulosa cells from small (1-5 mm) and large (8-22 mm) follicles were collected from bovine ovaries and cultured for 48 h in medium containing 10% fetal calf serum and then treated with various hormones in serum-free medium for an additional 48 h. We evaluated the effects of GDF-9 (150-600 ng/ml) and BMP-4 (30 ng/ml) during a 2-day exposure on hormone-induced steroidogenesis and cell proliferation. In FSH plus IGF-I-treated granulosa cells obtained from small follicles, 300 ng/ml GDF-9 reduced (P < 0.05) progesterone production by 15% and 600 ng/ml GDF-9 completely blocked (P < 0.01) the IGF-I-induced increase in progesterone production. In comparison, 300 and 600 ng/ml GDF-9 decreased (P < 0.05) estradiol production by 27% and 71% respectively, whereas 150 ng/ml GDF-9 was without effect (P > 0.10). Treatment with 600 ng/ml GDF-9 increased (P < 0.05) numbers (by 28%) of granulosa cells from small follicles. In the same cells treated with FSH but not IGF-I, co-treatment with 600 ng/ml GDF-9 decreased (P < 0.05) progesterone production (by 28%), increased (P < 0.05) cell numbers (by 60%), and had no effect (P > 0.10) on estradiol production. In FSH plus IGF-I-treated granulosa cells obtained from large follicles, GDF-9 caused a dose-dependent decrease (P<0.05) in IGF-I-induced progesterone (by 13-48%) and estradiol (by 20-51%) production. In contrast, GDF-9 increased basal and IGF-I-induced granulosa cell numbers by over 2-fold. Furthermore, treatment with BMP-4 also inhibited (P < 0.05) steroidogenesis by 27-42% but had no effect on cell numbers. To elucidate downstream signaling pathways, granulosa cells from small follicles were transfected with similar to mothers against decapentaplegics (Smad) binding element (CAGA)- or BMP response element (BRE)-promoter reporter constructs. Treatment with GDF-9 (but not BMP-4) activated the Smad3-induced CAGA promoter activity, whereas BMP-4 (but not GDF-9) activated the Smad1/5/8-induced BRE promoter activity. We have concluded that bovine granulosa cells are targets of both GDF-9 and BMP-4, and that oocyte-derived GDF-9 may simultaneously promote granulosa cell proliferation and prevent premature differentiation of the granulosa cells during growth of follicles, whereas theca-derived BMP-4 may also prevent premature follicular differentiation.
除促性腺激素外,卵泡发育过程中颗粒细胞的类固醇生成和增殖受多种卵巢内因子调控,包括生长分化因子9(GDF-9)、骨形态发生蛋白4(BMP-4)和胰岛素样生长因子I(IGF-I)。本研究的目的是确定GDF-9和BMP-4及其与IGF-I和促卵泡素(FSH)的相互作用对牛卵巢颗粒细胞功能的影响。从小(1 - 5毫米)和大(8 - 22毫米)卵泡收集牛卵巢颗粒细胞,在含10%胎牛血清的培养基中培养48小时,然后在无血清培养基中用各种激素再处理48小时。我们评估了2天暴露期间GDF-9(150 - 600纳克/毫升)和BMP-4(30纳克/毫升)对激素诱导的类固醇生成和细胞增殖的影响。在从小卵泡获得的经FSH加IGF-I处理的颗粒细胞中,300纳克/毫升GDF-9使孕酮生成减少(P < 0.05)15%,600纳克/毫升GDF-9完全阻断(P < 0.01)IGF-I诱导的孕酮生成增加。相比之下,300和600纳克/毫升GDF-9分别使雌二醇生成减少(P < 0.05)27%和71%,而150纳克/毫升GDF-9无作用(P > 0.10)。用600纳克/毫升GDF-9处理使小卵泡颗粒细胞数量增加(P < 0.05)(增加28%)。在经FSH但未用IGF-I处理的相同细胞中,与600纳克/毫升GDF-9共同处理使孕酮生成减少(P < 0.05)(减少28%),细胞数量增加(P < 0.05)(增加60%),对雌二醇生成无作用(P > 0.10)。在从大卵泡获得的经FSH加IGF-I处理的颗粒细胞中,GDF-9导致IGF-I诱导的孕酮(减少13 - 48%)和雌二醇(减少20 - 51%)生成呈剂量依赖性降低(P<0.05)。相反,GDF-9使基础和IGF-I诱导的颗粒细胞数量增加超过2倍。此外,用BMP-4处理也抑制(P < 0.05)类固醇生成27 - 42%,但对细胞数量无作用。为阐明下游信号通路,用类似于抗dpp蛋白结合元件(CAGA)或BMP反应元件(BRE)启动子报告构建体转染小卵泡颗粒细胞。用GDF-9(而非BMP-4)处理激活Smad3诱导的CAGA启动子活性,而BMP-4(而非GDF-9)激活Smad1/5/8诱导的BRE启动子活性。我们得出结论,牛颗粒细胞是GDF-9和BMP-4的靶细胞,卵母细胞来源的GDF-9可能在卵泡生长过程中同时促进颗粒细胞增殖并防止颗粒细胞过早分化,而卵泡膜来源的BMP-4也可能防止卵泡过早分化。