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在无血清培养基中诱导肌源性分化不需要DNA合成。

Induction of myogenic differentiation in serum-free medium does not require DNA synthesis.

作者信息

Pinset C, Whalen R G

出版信息

Dev Biol. 1985 Apr;108(2):284-9. doi: 10.1016/0012-1606(85)90032-6.

Abstract

Cells of the myogenic rat cell line L6 can be obtained as a confluent, quiescent population of undifferentiated myoblasts after growth in F12 medium supplemented with fetal calf serum. Myogenic differentiation can be induced in these cells by changing to Dulbecco's modified Eagle's (DME) medium containing insulin as the only protein component. Labeling of the cells with [3H]thymidine demonstrates that this induction of fusion occurs in the absence of DNA synthesis in about 85% of the cells. This result was confirmed using cytosine arabinoside: fusion of quiescent L6 cells was induced in the presence of this inhibitor of DNA synthesis. The myotubes formed in DME + insulin medium, with or without cytosine arabinoside, synthesize or accumulate proteins characteristic of differentiated muscle cells including myosin heavy and light chains, alpha-actin, alpha- and beta-tropomyosins, and the acetylcholine receptor. These experiments represent a direct demonstration that DNA synthesis is not required for the induction of myogenic differentiation in undifferentiated quiescent cells.

摘要

在添加胎牛血清的F12培养基中生长后,可获得成肌大鼠细胞系L6的细胞,它们是汇合的、静止的未分化成肌细胞群体。通过更换为仅含胰岛素作为唯一蛋白质成分的杜尔贝科改良伊格尔(DME)培养基,可诱导这些细胞发生成肌分化。用[3H]胸腺嘧啶核苷对细胞进行标记表明,约85%的细胞在不进行DNA合成的情况下发生这种融合诱导。使用阿糖胞苷证实了这一结果:在这种DNA合成抑制剂存在的情况下,诱导静止的L6细胞融合。在含或不含阿糖胞苷的DME + 胰岛素培养基中形成的肌管合成或积累了分化肌肉细胞特有的蛋白质,包括肌球蛋白重链和轻链、α - 肌动蛋白、α - 和β - 原肌球蛋白以及乙酰胆碱受体。这些实验直接证明,未分化的静止细胞诱导成肌分化不需要DNA合成。

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