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牛卵泡膜细胞和颗粒细胞体外分化为小黄体样细胞和大黄体样细胞:形态学和功能特征

In vitro differentiation of bovine theca and granulosa cells into small and large luteal-like cells: morphological and functional characteristics.

作者信息

Meidan R, Girsh E, Blum O, Aberdam E

机构信息

Department of Animal Science, Faculty of Agriculture, Hebrew University of Jerusalem, Rehovot, Israel.

出版信息

Biol Reprod. 1990 Dec;43(6):913-21. doi: 10.1095/biolreprod43.6.913.

Abstract

This study was undertaken to investigate whether bovine granulosa and theca interna cells could be luteinized in vitro into luteal-like cells. Granulosa and theca cells were cultured for 9 days in the presence of forskolin (10 microM), insulin (2 micrograms/ml), insulin-like growth factor I (100 ng/ml), or a combination of these agents. During the first day of culture, granulosa and theca cells secreted estradiol and androstenedione, respectively; progesterone rose only after 3-5 days in culture and reached a maximum on the ninth day of culture. Cells incubated in the presence of forskolin plus insulin exhibited morphological and functional characteristics of luteal cells isolated from the corpus luteum. It was found that cell diameter, basal and stimulated progesterone secretion, and pattern of cell replication for both cell types were comparable to those of luteal cells. Numerous lipid droplets and intensified mitochondrial adrenodoxin staining also indicated active steroidogenesis in luteinized cells. After 9 days in culture, stimulants were withdrawn, and the culture proceeded in basal medium for an additional 5 days; elevated progesterone levels were maintained by luteinized granulosa cells (LGC), whereas in contrast a dramatic drop in progesterone production was observed in luteinized theca cells (LTC). On Day 9, cells were challenged for 3 h with LH (10 ng/ml), forskolin (10 microM), or cholera toxin (100 ng/ml), resulting in a 4-fold increase in progesterone secretion by LTC; the same treatments failed to stimulate progesterone in LGC.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

本研究旨在探讨牛颗粒细胞和卵泡内膜细胞能否在体外黄体化成为黄体样细胞。颗粒细胞和卵泡膜细胞在存在福斯高林(10微摩尔)、胰岛素(2微克/毫升)、胰岛素样生长因子I(100纳克/毫升)或这些因子组合的情况下培养9天。在培养的第一天,颗粒细胞和卵泡膜细胞分别分泌雌二醇和雄烯二酮;孕酮仅在培养3 - 5天后升高,并在培养的第九天达到最大值。在福斯高林加胰岛素存在下孵育的细胞表现出从黄体分离出的黄体细胞的形态和功能特征。发现两种细胞类型的细胞直径、基础和刺激后的孕酮分泌以及细胞复制模式与黄体细胞相当。大量脂滴和增强的线粒体肾上腺皮质铁氧化还原蛋白染色也表明黄体化细胞中有活跃的类固醇生成。培养9天后,撤除刺激物,在基础培养基中再培养5天;黄体化颗粒细胞(LGC)维持孕酮水平升高,而相比之下,黄体化卵泡膜细胞(LTC)中观察到孕酮产生急剧下降。在第9天,用促黄体生成素(10纳克/毫升)、福斯高林(10微摩尔)或霍乱毒素(100纳克/毫升)刺激细胞3小时,导致LTC的孕酮分泌增加4倍;相同处理未能刺激LGC中的孕酮分泌。(摘要截断于250字)

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