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培养的子宫肌层细胞中17β-羟类固醇脱氢酶活性:连续传代培养的影响。

17 beta-hydroxysteroid dehydrogenase activity in cultured myometrial cells: effect of serial subcultures.

作者信息

Vallet-Strouve C, Fresinsky E, Mowszowicz I

出版信息

J Steroid Biochem. 1982 Jul;17(1):95-100. doi: 10.1016/0022-4731(82)90598-2.

Abstract

17 beta-Hydroxysteroid dehydrogenase (17 beta-SDH) activity was studied in culture ovine myometrial cells. After primary culture, cells were routinely subcultured (every 7th day), seeded at 5 x 10(5) cells per dish and grown in a medium with 2% of serum. 17 beta-SDH activity was measured by incubating intact cell monolayers with [3H]-estradiol (5 x 10(-9) M) in serum-free medium. Metabolites were extracted from both cells and medium, and separated by thin-layer chromatography. 17 beta-SDH was expressed as total E1 formed (cells + medium) in fmol/mg of protein as a function of time. 17 beta-SDH has an approximate Km of 5 x 10(-6) M. After 3 min of incubation, all measurable E1 is within the cells; it is progressively released but after 1 h only 40% of E1 is found in the medium. 17 beta-SDH decreases from day 2 to day 8 of each subculture, whereas total proteins increase. Subculture partially restores 17 beta-SDH activity so that it is always higher on day 2 of any subculture than on day 8 of the previous one, however a progressive decline occurs with successive subcultures. This decline parallels the slowing of cell growth and overall protein synthesis and probably reflects cell ageing.

摘要

在培养的绵羊子宫肌层细胞中研究了17β-羟类固醇脱氢酶(17β-SDH)的活性。原代培养后,细胞按常规传代培养(每7天传代一次),每皿接种5×10⁵个细胞,并在含2%血清的培养基中生长。通过在无血清培养基中将完整的细胞单层与[³H]-雌二醇(5×10⁻⁹ M)孵育来测定17β-SDH的活性。从细胞和培养基中提取代谢物,并通过薄层色谱法进行分离。17β-SDH以每毫克蛋白质中形成的总E1(细胞 + 培养基)表示,作为时间的函数。17β-SDH的近似Km为5×10⁻⁶ M。孵育3分钟后,所有可测量的E1都在细胞内;它逐渐释放,但孵育1小时后,仅40%的E1存在于培养基中。在每次传代培养中,17β-SDH从第2天到第8天减少,而总蛋白增加。传代培养部分恢复了17β-SDH的活性,因此在任何传代培养的第2天它总是高于上一代的第8天,然而随着连续传代培养会出现逐渐下降。这种下降与细胞生长和总体蛋白质合成的减慢平行,可能反映了细胞衰老。

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