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大鼠黄体化颗粒细胞对人促甲状腺激素的体外反应

In vitro responses of luteinizing rat granulosa cells to human thyroid-stimulating hormone.

作者信息

Grasso P, Crisp T M

出版信息

Biol Reprod. 1985 May;32(4):935-45. doi: 10.1095/biolreprod32.4.935.

Abstract

The effect of human thyroid-stimulating hormone (hTSH) on progesterone (P4) secretion during initial luteinization and subsequent prolactin (Prl)-mediated steroidogenesis by cultured rat granulosa cells was studied. Granulosa cells, obtained from pregnant mare's serum gonadotropin (PMSG)-treated immature female rats, were preincubated for 1, 3, 6, 12, or 24 h in control medium lacking added hormones or in medium containing 1.0 microgram/ml human chorionic gonadotropin (hCG) or hTSH, and maintained subsequently for 6 days in medium containing 1.0 microgram/ml bovine (bPrl). Indices of luteotropic stimulation were provided by: 1) elevated P4 concentrations determined by radioimmunoassay of spent media samples; and 2) cytoplasmic lipid accumulation assessed by osmium tetroxide staining following fixation after 7 days of culture. Progesterone levels in media from cultures exposed to hCG for 24 h were twofold higher than control cultures, whereas those in media from cultures preincubated in hTSH for 24 h were fourfold higher than control levels. Cultures preincubated in 1.0 microgram/ml hCG for as little as 1 h and then maintained for 6 days in Prl secreted significantly more P4 than did control cultures also maintained with Prl for 6 days. Cultures preincubated in hTSH required a 24-h exposure before a significant increase in Prl-mediated P4 secretion was observed. Intensity of cytoplasmic osmiophilia correlated directly with P4 concentration. These results suggest that: 1) hTSH has the ability to promote P4 secretion during initial luteinization and to regulate subsequent Prl-mediated steroidogenesis by cultured rat granulosa cells; and 2) the mechanism by which hTSH stimulates Prl-mediated P4 secretion in this model system may differ from that of hCG.

摘要

研究了人促甲状腺激素(hTSH)对培养的大鼠颗粒细胞在初始黄体化过程中孕酮(P4)分泌以及随后催乳素(Prl)介导的类固醇生成的影响。从经孕马血清促性腺激素(PMSG)处理的未成熟雌性大鼠获取颗粒细胞,将其在缺乏添加激素的对照培养基中或在含有1.0微克/毫升人绒毛膜促性腺激素(hCG)或hTSH的培养基中预孵育1、3、6、12或24小时,随后在含有1.0微克/毫升牛催乳素(bPrl)的培养基中维持6天。黄体生成刺激指标包括:1)通过放射免疫分析法测定用过的培养基样本中的P4浓度升高;2)培养7天后固定,通过四氧化锇染色评估细胞质脂质积累。暴露于hCG 24小时的培养物培养基中的孕酮水平比对照培养物高两倍,而在hTSH中预孵育24小时的培养物培养基中的孕酮水平比对照水平高四倍。在1.0微克/毫升hCG中预孵育仅1小时然后在Prl中维持6天的培养物分泌的P4明显多于同样在Prl中维持6天的对照培养物。在hTSH中预孵育的培养物需要暴露24小时才能观察到Prl介导的P4分泌显著增加。细胞质嗜锇性强度与P4浓度直接相关。这些结果表明:1)hTSH有能力在初始黄体化过程中促进P4分泌,并调节培养的大鼠颗粒细胞随后Prl介导的类固醇生成;2)在该模型系统中,hTSH刺激Prl介导的P4分泌的机制可能与hCG不同。

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