Development of a long-term serum-free culture system for immature granulosa cells from diethylstilboestrol-treated prepubertal rabbits: influence of androstenedione and fibronectin on FSH-induced cytodifferentiation.
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引用次数: 3
Abstract
Granulosa cells from diethylstilboestrol-treated prepubertal rabbits were cultured for 6 days in M199 with FSH (1-100 ng ml(-1)) in uncoated or fibronectin-coated plates with or without androstenedione to define the time course profile of oestradiol and progesterone secretion, and the possible modulator role of androstenedione and fibronectin during FSH-induced rabbit granulosa cell differentiation. Every 48 h, cultures were photographed and samples of medium were collected and assayed by ELISA for oestradiol and progesterone. FSH increased oestradiol secretion in a dose-dependent manner. Androstenedione augmented FSH-stimulated oestradiol secretion, and led to a decrease in secretion of oestradiol with time in culture. FSH stimulated progesterone secretion in a dose-dependent manner. This was increased by androstenedione with 10 ng FSH ml(-1) (0-96 h) and 1 ng FSH ml(-1) (96-144 h). FSH-stimulated (100 ng ml(-1)) progesterone secretion decreased at 48-96 h. Fibronectin prevented this decrease, without affecting oestradiol or progesterone secretion at other time points. FSH caused cell reaggregation at 48 h. In conclusion, this serum-free culture system is appropriate for the study of mechanisms of rabbit granulosa cell differentiation. FSH induced cytodifferentiation and reaggregation of granulosa cells. Androstenedione appeared to act synergistically with FSH to promote steroidogenesis. Fibronectin sustained progesterone secretion during differentiation.
将经己烯雌酚处理的青春期前家兔颗粒细胞在含FSH (1-100 ng ml(-1))的M199培养皿中培养6天,在未包被或未包被雄烯二酮或纤维连接蛋白包被的培养皿中培养6天,以确定雌二醇和黄体酮分泌的时间过程,以及雄烯二酮和纤维连接蛋白在FSH诱导的家兔颗粒细胞分化过程中可能的调节作用。每隔48 h对培养物拍照,收集培养基样品,ELISA检测雌二醇和黄体酮含量。卵泡刺激素增加雌二醇分泌呈剂量依赖性。雄烯二酮增强了fsh刺激的雌二醇分泌,并导致雌二醇分泌随培养时间的增加而减少。卵泡刺激素刺激黄体酮分泌呈剂量依赖性。雄烯二酮添加10 ng FSH ml(-1) (0-96 h)和1 ng FSH ml(-1) (96-144 h)可增加黄体酮的分泌,FSH刺激(100 ng ml(-1))在48-96 h时黄体酮分泌减少,纤维连接蛋白阻止了这种减少,在其他时间点不影响雌二醇或黄体酮分泌。综上所述,该无血清培养系统适合于兔颗粒细胞分化机制的研究。FSH诱导颗粒细胞分化和再聚集。雄烯二酮似乎与卵泡刺激素协同作用,促进类固醇生成。纤维连接蛋白维持分化过程中黄体酮的分泌。