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Numb-dependent integration of pre-TCR and p53 function in T-cell precursor development

机译:T细胞前体发育中预TCR和P53功能的Numb依赖性集成

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摘要

Numb asymmetrically segregates at mitosis to control cell fate choices during development. Numb inheritance specifies progenitor over differentiated cell fates, and, paradoxically, also promotes neuronal differentiation, thus indicating that the role of Numb may change during development. Here we report that Numb nuclear localization is restricted to early thymocyte precursors, whereas timed appearance of pre-T-cell receptor (pre-TCR) and activation of protein kinase C θ promote phosphorylation-dependent Numb nuclear exclusion. Notably, nuclear localization of Numb in early thymocyte precursors favors p53 nuclear stabilization, whereas pre-TCR-dependent Numb nuclear exclusion promotes the p53 downmodulation essential for further differentiation. Accordingly, the persistence of Numb in the nucleus impairs the differentiation and promotes precursor cell death. This study reveals a novel regulatory mechanism for Numb function based on its nucleus–cytosol shuttling, coupling the different roles of Numb with different stages of T-cell development.
机译:麻木在有丝分裂时不对称隔离,以控制在开发过程中控制细胞命运选择。 Numb继承指定渗透细胞序列的祖细胞,并且矛盾的是,促进神经元分化,从而表明麻木的作用可能在开发过程中改变。在这里,我们报告说,Numb核定位限于早期胸腺细胞前体,而预T细胞受体(预TCR)的定时外观和蛋白激酶Cθ的活化促进磷酸化依赖性Numb核排斥。值得注意的是,早期胸腺细胞前体中麻木的核定位有利于P53核稳定,而预先依赖性麻木核排除促进了对进一步分化的P53拨款。因此,核中麻木的持续存在损害分化并促进前体细胞死亡。本研究揭示了基于其核 - 胞嘧啶梭的Numb功能的新调节机制,偶联了与T细胞发育不同阶段的Numb的不同作用。

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