首页> 美国卫生研究院文献>The Journal of Neuroscience >A Crucial Role for p57Kip2 in the Intracellular Timer that Controls Oligodendrocyte Differentiation
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A Crucial Role for p57Kip2 in the Intracellular Timer that Controls Oligodendrocyte Differentiation

机译:p57Kip2在控制少突胶质细胞分化的细胞内定时器中的关键作用。

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摘要

The intracellular molecular mechanism that controls the timing of oligodendrocyte differentiation remains unknown. previously showed that an oligodendrocyte precursor cell (OPC) can divide a maximum of approximately eight times before its daughter cells simultaneously cease proliferating and differentiate into oligodendrocytes. They postulated that over time the level of an intracellular molecule might synchronously change in each daughter cell, ultimately reaching a level that prohibited additional proliferation. Here, we report the discovery of such a molecule, the cyclin-dependent kinase inhibitor p57Kip2 (Cdkn1c). We show in vitro that all daughters of a clone of OPCs express similar levels of p57Kip2, that p57Kip2 levels increase over time in proliferating OPCs, and that p57Kip2 levels regulate how many times an OPC can divide before differentiating. These findings reveal a novel part of the mechanism by which OPCs measure time and are likely to extend to similar timers in many other precursor cell types.
机译:控制少突胶质细胞分化时间的细胞内分子机制仍然未知。以前的研究表明,少突胶质细胞前体细胞(OPC)最多可以分裂约八倍,然后其子细胞同时停止增殖并分化为少突胶质细胞。他们推测,随着时间的流逝,每个子细胞中细胞内分子的水平可能会同步变化,最终达到禁止进一步增殖的水平。在这里,我们报道了这种分子的发现,即周期蛋白依赖性激酶抑制剂p57 Kip2 (Cdkn1c)。我们在体外显示,OPC克隆的所有子代均表达相似水平的p57 Kip2 ,p57 Kip2 水平随着时间的增长而增加,而p57 Kip2 级别规定了OPC在区分之前可以划分的次数。这些发现揭示了OPC测量时间的机制中的一个新颖部分,并可能扩展到许多其他前体细胞类型中的类似计时器。

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