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建立一种在体外可分化为脂肪细胞的克隆细胞系。

Establishment of a clonal cell line that differentiates into adipose cells in vitro.

作者信息

Hiragun A, Sato M, Mitsui H

出版信息

In Vitro. 1980 Aug;16(8):685-93. doi: 10.1007/BF02619198.

Abstract

From the fibroblastic cells of murine mammary tumor tissue we isolated a clonal cell line that could be induced to differentiate into fat-accumulating cells in vitro. Differentiation began after the cultures had reached confluence and was accompanied by (a) an increase in the incorporation of sodium acetate into the triglyceride (TG) fraction of cellular lipids, (b) a more than 50-fold increase in cellular TG content per milligram cell-layer protein basis and (c) the cessation of cellular DNA synthesis. The addition of insulin to the culture medium enhanced lipid accumulation and increased the fraction of cells that differentiated into adipocytes. When insulin (5 to 10 microgram/ml) was added exogenously, 80% or more of the cells were induced to differentiate into mature adipocytes within 2 weeks. This cell line can be used as a model for mammalian cell differentiation and also as a convenient material for the study of lipid metabolism in adipocytes.

摘要

我们从小鼠乳腺肿瘤组织的成纤维细胞中分离出一种克隆细胞系,该细胞系在体外可被诱导分化为脂肪积累细胞。分化在培养物达到汇合后开始,并伴随着以下变化:(a)醋酸钠掺入细胞脂质甘油三酯(TG)部分的量增加;(b)以每毫克细胞层蛋白为基础,细胞TG含量增加了50倍以上;(c)细胞DNA合成停止。向培养基中添加胰岛素可增强脂质积累,并增加分化为脂肪细胞的细胞比例。当外源添加胰岛素(5至10微克/毫升)时,80%或更多的细胞在2周内被诱导分化为成熟脂肪细胞。该细胞系可作为哺乳动物细胞分化的模型,也可作为研究脂肪细胞脂质代谢的便利材料。

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