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The RNA-binding protein HuD regulates neuronal cell identity and maturation

机译:RNA结合蛋白HuD调节神经元细胞的身份和成熟

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摘要

Neural Hu proteins (HuB/C/D) are RNA-binding proteins that have been shown to induce neuronal differentiation activity when overexpressed in immature neural progenitor cells or undifferen-tiated neuronal tumors. Newly generated HuD-deficient mice exhibited a transient impaired-cranial-nerve-development pheno-type at an early embryonic stage. Adult HuD-deficient mice exhibited an abnormal hind-limb reflex and poor rotarod performance. Analysis of neurosphere formation revealed that the number and self-renewal capacity of the neural stem/progenitor cells were increased in HuD-deficient mice. HuD-deficient primary neu-rospheres also generated a smaller number of neurons. Cohort analysis of the cellular proliferative activity by using BrdUrd and iododeoxuridine labeling revealed that the number of differentiating quiescent cells in the embryonic cerebral wall was decreased. Long-term administration of BrdUrd revealed that the number of slowly dividing stem cells in the adult subventricular zone was increased in the HuD-deficient mice. Taken together, the results suggest that HuD is required at multiple points during neuronal development, including negative regulation of proliferative activity and neuronal cell-fate acquisition of neural stem/progenitor cells.
机译:神经Hu蛋白(HuB / C / D)是RNA结合蛋白,在未成熟的神经祖细胞或未分化的神经元肿瘤中过表达时,已显示出诱导神经元分化的作用。新生的HuD缺陷小鼠在早期胚胎期表现出短暂的颅神经发育异常表型。成年的HuD缺陷小鼠表现出异常的后肢反射和不良的轮转表现。对神经球形成的分析表明,HuD缺陷小鼠神经干/祖细胞的数量和自我更新能力增加。缺乏HuD的初级神经球也产生了较少数量的神经元。通过使用BrdUrd和碘脱氧尿苷标记对细胞增殖活性进行的队列分析显示,胚胎脑壁中分化静止细胞的数量减少了。长期服用BrdUrd显示,在缺HuD的小鼠中,成年脑室下区域中缓慢分裂的干细胞数量增加了。两者合计,结果表明在神经元发育过程中的多个点都需要HuD,包括增殖活性的负调控和神经干/祖细胞的神经元命运的采集。

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