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转化生长因子-β对仓鼠腔前卵泡中促卵泡激素诱导的脱氧核糖核酸合成的增强作用是由表皮生长因子的潜在诱导介导的。

Transforming growth factor-beta potentiation of follicle-stimulating hormone-induced deoxyribonucleic acid synthesis in hamster preantral follicles is mediated by a latent induction of epidermal growth factor.

作者信息

Roy S K

机构信息

Department of Obstetrics and Gynecology, University of Nebraska Medical Center, Omaha 68198-4515.

出版信息

Biol Reprod. 1993 Mar;48(3):558-63. doi: 10.1095/biolreprod48.3.558.

Abstract

The mechanisms of transforming growth factor-beta (TGF-beta) potentiation of FSH action on follicular DNA synthesis in the hamster were investigated by use of TGF-beta (beta 1 and beta 2) and a potent epidermal growth factor (EGF)-specific polyclonal antibody. Preantral follicles at stages 1-6 and early antral follicles at stage 7 were enzymatically and mechanically isolated from adult golden hamsters on proestrus. Follicles were incubated in Dulbecco's modified Eagle's medium with ITS+ (6.25 micrograms insulin, 6.25 micrograms transferrin, 6.25 micrograms selenium, 1.25 mg BSA, and 5.35 micrograms linoleic acid/ml) hydrocortisone, and 1 microCi/ml [3H]thymidine. Follicles were exposed for 24 h to FSH (100 ng/ml), TGF-beta 1, and TGF-beta 2 (1 and 10 ng/ml), EGF antibody (50 microliters/ml), and TGF-alpha (50 ng/ml) under various experimental conditions. Both TGF-beta 1 and TGF-beta 2 significantly potentiated FSH-induced follicular DNA synthesis; however, the effect was drastically attenuated by EGF antibody. EGF antibody also inhibited FSH-induced follicular [3H]thymidine incorporation. TGF-beta 2 potentiation of FSH action was also significantly inhibited by a second dose of TGF-beta 2 when added 6 h after the beginning of culture; however, follicles at different stages responded differently to the second dose of TGF-beta 2. For example, when the second dose of TGF-beta 2 was added 14 h after the first dose, only the large preantral follicles at stages 4-6 were affected. Interestingly, the second dose of TGF-beta 2 also inhibited TGF-beta 2-induced DNA synthesis.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

通过使用转化生长因子-β(TGF-β,β1和β2)以及一种有效的表皮生长因子(EGF)特异性多克隆抗体,研究了仓鼠中转化生长因子-β增强促卵泡激素(FSH)对卵泡DNA合成作用的机制。在动情前期,从成年金黄仓鼠中酶解并机械分离出1-6期的窦前卵泡和7期的早期窦卵泡。将卵泡在含有ITS+(6.25微克胰岛素、6.25微克转铁蛋白、6.25微克硒、1.25毫克牛血清白蛋白和5.35微克亚油酸/毫升)、氢化可的松和1微居里/毫升[3H]胸腺嘧啶核苷的杜氏改良 Eagle 培养基中培养。在各种实验条件下,将卵泡暴露于FSH(100纳克/毫升)、TGF-β1和TGF-β2(1和10纳克/毫升)、EGF抗体(50微升/毫升)和TGF-α(50纳克/毫升)24小时。TGF-β1和TGF-β2均显著增强了FSH诱导的卵泡DNA合成;然而,EGF抗体可显著减弱这种作用。EGF抗体也抑制了FSH诱导的卵泡[3H]胸腺嘧啶核苷掺入。当在培养开始6小时后添加第二剂TGF-β2时,TGF-β2对FSH作用的增强也被显著抑制;然而,不同阶段的卵泡对第二剂TGF-β2的反应不同。例如,当在第一剂后14小时添加第二剂TGF-β2时,仅4-6期的大型窦前卵泡受到影响。有趣的是,第二剂TGF-β2也抑制了TGF-β2诱导的DNA合成。(摘要截短于250字)

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