首页> 外文期刊>Molecular and Cellular Endocrinology >Comparison of oocyte factors and transforming growth factor-beta in the regulation of DNA synthesis in bovine granulosa cells.
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Comparison of oocyte factors and transforming growth factor-beta in the regulation of DNA synthesis in bovine granulosa cells.

机译:比较卵母细胞因子和转化生长因子-β在调节牛颗粒细胞DNA合成中的作用。

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摘要

Oocytes are powerful local modulators of follicular cell functions and many of the activities of oocytes are attributed to members of the transforming growth factor-beta (TGF-beta) superfamily. Whilst in the mouse it is known that members of this family are able to mimic many of the effects of oocytes on follicular cells, the relative importance of any of these factors is unknown in bovine follicles. The objectives of this study were to determine if bovine oocytes express and secrete TGF-beta and to compare oocyte-secreted factor(s) to TGF-beta in terms of their capacities to stimulate mural granulosa cell (MGC) DNA synthesis. Bovine ovaries were collected from an abattoir and RNA was extracted from isolated MGC, cumulus cells, cumulus-oocyte complexes and denuded oocytes (DO). Using RT-PCR, all cell types were found to express TGF-beta1 and TGF-beta2 mRNA transcripts. However, no TGF-beta bioactivity could be detected from DO using a sensitive (40 pg/ml) and specific mink lung fibroblast cell bioassay. MGC were cultured with various combinations and doses of TGF-beta2 and DO for 18 h, followed by a 6-h pulse of [3H]-thymidine as an indicator of cellular DNA synthesis. MGC DNA synthesis was stimulated by both TGF-beta2 and DO. However in response to increasing doses of TGF-beta2, [3H]-thymidine levels plateaued at <2-fold above control levels, whereas levels continued to increase over the dose range of DO tested (up to 3.4-fold). Addition of a TGF-beta pan-specific neutralising antibody to MGC cultures eliminated the TGF-beta2-stimulatory effects on DNA synthesis and the TGF-beta2-suppressive effects on progesterone production, but the antibody was unable to neutralise the same responses when induced by DO. These results support a role for TGF-beta1, TGF-beta2 and DO in paracrine/autocrine regulation of bovine granulosa cell function, but indicate that neither TGF-beta1 nor TGF-beta2 can account for the actions of bovine oocytes on granulosa cells.
机译:卵母细胞是卵泡细胞功能的强大局部调节剂,卵母细胞的许多活动都归因于转化生长因子-β(TGF-β)超家族的成员。虽然在小鼠中已知该家族的成员能够模仿卵母细胞对卵泡细胞的许多作用,但在牛卵泡中尚不清楚这些因素中任何一种的相对重要性。这项研究的目的是确定牛卵母细胞是否表达和分泌TGF-β,并比较卵母细胞分泌的因子与TGF-β刺激壁颗粒细胞(MGC)DNA合成的能力。从屠宰场收集牛卵巢,并从分离的MGC,卵丘细胞,卵丘卵母细胞复合物和裸露的卵母细胞(DO)中提取RNA。使用RT-PCR,发现所有细胞类型均表达TGF-beta1和TGF-beta2 mRNA转录本。但是,使用灵敏的(40 pg / ml)和特异性的水貂肺成纤维细胞生物测定法不能从DO中检测到TGF-beta的生物活性。用各种组合和剂量的TGF-beta2和DO培养MGC 18小时,然后脉冲[3H]-胸苷6小时作为细胞DNA合成的指示剂。 TGC-beta2和DO都刺激了MGC DNA的合成。然而,响应于增加的TGF-β2剂量,[3 H]-胸苷水平稳定在对照水平的<2倍,而水平在所测试的DO的剂量范围内持续增加(高达3.4倍)。向MGC培养物中添加TGF-β泛特异性中和抗体消除了TGF-β2-对DNA合成的刺激作用以及TGF-β2-对孕酮产生的抑制作用,但是当由TGF-β泛特异性中和抗体诱导时,该抗体无法中和相同的反应做。这些结果支持TGF-beta1,TGF-beta2和DO在旁分泌/自分泌调节牛颗粒细胞功能中的作用,但表明TGF-beta1和TGF-beta2都不能解释牛卵母细胞对颗粒细胞的作用。

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