Gangrade B K, May J V
Department of Obstetrics and Gynecology, University of Kansas School of Medicine, Wichita.
Endocrinology. 1990 Nov;127(5):2372-80. doi: 10.1210/endo-127-5-2372.
Porcine granulosa cells isolated from small (1-3 mm in diameter) follicles proliferate rapidly in culture in response to 10% fetal bovine serum (FBS) and epidermal growth factor (EGF) (10 ng/ml). Transforming growth factor-beta (TGF beta) inhibits FBS/EGF-stimulated proliferation in a dose-dependent manner. We have used this proliferation inhibitory property of TGF beta to assay qualitatively, the presence of this growth factor in conditioned medium from cultured follicle cells as well as in partially purified preparations from porcine ovarian compartments. In addition, the concentration of TGF beta in the theca cell conditioned medium was quantitatively estimated by generating a TGF beta-dose-response curve (inhibition of FBS/EGF-stimulated proliferation of granulosa cells in monolayer culture) using authentic human TGF beta-1. Ovarian thecal cells isolated from small and large size follicles in the pig ovary secrete TGF beta-like activity in vitro. Medium conditioned by thecal cells in primary monolayer culture contains a latent form of TGF beta which can be activated by heat or acid treatment. In contrast, and unlike rat granulosa cells, porcine granulosa cells in primary monolayer culture do not secrete detectable levels of TGF beta-like activity in the medium. Incubation of heat-activated thecal cell conditioned medium with a TGF beta-neutralizing antibody (which recognizes TGF beta-1 and 2) but not nonimmune serum attenuated the TGF beta-like activity in thecal cell conditioned medium suggesting that this activity is due to authentic TGF beta. Since many cell types secrete latent TGF beta in the medium when cultured in vitro, we next investigated whether thecal cell secretion of latent TGF beta was a function of cell culture or whether the ovarian thecal compartment actually contained detectable levels of TGF beta-like activity. To this end, we used an acid-ethanol extraction procedure to isolate thecal proteins from fresh-frozen tissue. The acid-ethanol extracted protein fraction was mixed with trace amounts of 125I-TGF beta for detection and chromatographed on Bio-Gel P-60 column under acidic conditions. Elution of TGF beta bioactivity from the Bio-Gel P-60 column as measured by inhibition of granulosa cell proliferation correlated with the elution of radioiodinated authentic TGF beta. Preincubation of TGF beta-like activity-containing fractions with TGF beta-neutralizing antibody attenuated the proliferation-inhibitory activity in these fractions. TGF beta activity was also observed in fractions extracted from porcine corpora lutea.(ABSTRACT TRUNCATED AT 400 WORDS)
从直径为1 - 3毫米的小卵泡中分离出的猪颗粒细胞,在含有10%胎牛血清(FBS)和表皮生长因子(EGF,10纳克/毫升)的培养基中培养时会迅速增殖。转化生长因子-β(TGF-β)以剂量依赖的方式抑制FBS/EGF刺激的增殖。我们利用TGF-β的这种增殖抑制特性,定性分析培养的卵泡细胞条件培养基以及猪卵巢各部分的部分纯化制剂中这种生长因子的存在情况。此外,通过使用 authentic human TGF-β-1生成TGF-β剂量反应曲线(抑制单层培养的颗粒细胞中FBS/EGF刺激的增殖),定量估计了卵泡膜细胞条件培养基中TGF-β的浓度。从猪卵巢中小卵泡和大卵泡分离出的卵巢卵泡膜细胞在体外分泌TGF-β样活性物质。原代单层培养的卵泡膜细胞条件培养基中含有一种潜伏形式的TGF-β,可通过加热或酸处理激活。相比之下,与大鼠颗粒细胞不同,原代单层培养的猪颗粒细胞在培养基中不分泌可检测水平的TGF-β样活性物质。用TGF-β中和抗体(识别TGF-β-1和2)而非非免疫血清孵育热激活的卵泡膜细胞条件培养基,可减弱卵泡膜细胞条件培养基中的TGF-β样活性,这表明这种活性是由 authentic TGF-β引起的。由于许多细胞类型在体外培养时会在培养基中分泌潜伏的TGF-β,我们接下来研究卵泡膜细胞分泌潜伏TGF-β是细胞培养的作用,还是卵巢卵泡膜部分实际上含有可检测水平的TGF-β样活性物质。为此,我们使用酸 - 乙醇提取程序从新鲜冷冻组织中分离卵泡膜蛋白。将酸 - 乙醇提取的蛋白部分与微量的125I - TGF-β混合用于检测,并在酸性条件下在Bio - Gel P - 60柱上进行色谱分析。通过抑制颗粒细胞增殖测量的Bio - Gel P - 60柱上TGF-β生物活性的洗脱与放射性碘化 authentic TGF-β的洗脱相关。用TGF-β中和抗体预孵育含有TGF-β样活性的部分可减弱这些部分中的增殖抑制活性。在从猪黄体中提取的部分中也观察到了TGF-β活性。(摘要截短至400字)