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L6成肌细胞中调节肌生成的因子的表达增强。

The amplified expression of factors regulating myogenesis in L6 myoblasts.

作者信息

Wright W E

出版信息

J Cell Biol. 1985 Jan;100(1):311-6. doi: 10.1083/jcb.100.1.311.

Abstract

A strategy for increasing the expression of the factors regulating myogenesis was developed based upon the observation that increased amounts of regulatory factors could overcome the inhibition of differentiation produced by 5-bromodeoxyuridine (BUdR). L6 rat myoblasts were subjected to multiple cycles of cloning in progressively increasing concentrations of BUdR. The first clones to differentiate were picked and replated for the next cycle of selection. After 28 cycles in BUdR, cells were isolated that could differentiate in the presence of 8 microM BUdR. Cell hybrids between myoblasts subjected to 21 cycles of selection (BU21 cells) and differentiation-defective myoblasts exhibited a high probability of differentiation, consistent with the hypothesis that BU21 cells were overproducing factor(s) involved in the decision to differentiate. The selection of cells able to differentiate in the presence of BUdR may provide a general approach for increasing the expression of the regulatory molecules controlling terminal differentiation.

摘要

基于以下观察结果制定了一种提高调节肌生成的因子表达的策略

即增加调节因子的量可以克服5-溴脱氧尿苷(BUdR)对分化的抑制作用。将L6大鼠成肌细胞置于浓度逐渐增加的BUdR中进行多个克隆循环。挑选出最早分化的克隆并重新接种以进行下一轮选择。在BUdR中经过28个循环后,分离出了在8微摩尔BUdR存在下仍能分化的细胞。经过21个选择循环的成肌细胞(BU21细胞)与分化缺陷型成肌细胞之间的细胞杂交体表现出很高的分化概率,这与BU21细胞过量产生参与分化决定的因子这一假设一致。选择在BUdR存在下能够分化的细胞可能为提高控制终末分化的调节分子的表达提供一种通用方法。

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Coexpression of myogenic functions in L6 rat x T984 mouse myoblast hybrids.
Dev Biol. 1981 Aug;86(1):236-40. doi: 10.1016/0012-1606(81)90335-3.

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