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miRNAs 在干细胞重编程中对神经元的诱导和分化作用。

miRNAs stem cell reprogramming for neuronal induction and differentiation.

机构信息

CTI-LYON, Cell Therapy Research Institute, Parc Technologique de Lyon Saint-Priest, Saint-Priest, Lyon, France.

出版信息

Mol Neurobiol. 2011 Jun;43(3):215-27. doi: 10.1007/s12035-011-8179-z. Epub 2011 Mar 29.

Abstract

Mimicking the natural brain environment during neurogenesis represents the main challenge for efficient in vitro neuronal differentiation of stem cells. The discovery of miRNAs opens new possibilities in terms of modulation of stem cells lineage commitment and differentiation. Many studies demonstrated that in vitro transient overexpression or inhibition of brain-specific miRNAs in stem cells significantly directed differentiation along neuronal cell lineages. Modulating miRNA expression offers new pathways for post-transcriptional gene regulation and stem cell commitment. Neurotrophins and neuropoietins signaling pathways are the main field of investigation for neuronal commitment, differentiation, and maturation. This review will highlight examples of crosstalk between stem-cell-specific and brain-specific signaling pathways and key miRNA candidates for neuronal commitment. Recent progress on understanding miRNAs genetic networks offers promising prospects for their increasing application in the development of new cellular therapies in humans.

摘要

在神经发生过程中模拟自然的大脑环境是干细胞有效体外神经元分化的主要挑战。miRNA 的发现为调节干细胞谱系定向和分化提供了新的可能性。许多研究表明,在体外瞬时过表达或抑制干细胞中的脑特异性 miRNA 可显著沿神经元细胞谱系指导分化。调节 miRNA 表达为转录后基因调控和干细胞定向提供了新的途径。神经营养因子和神经细胞因子信号通路是神经元定向、分化和成熟的主要研究领域。本综述将重点介绍干细胞特异性和脑特异性信号通路之间相互作用的实例,以及用于神经元定向的关键 miRNA 候选物。对 miRNA 遗传网络的理解的最新进展为其在人类新型细胞疗法开发中的应用提供了广阔的前景。

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