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MicroRNA 靶向的神经元重编程作为治疗神经系统疾病的一种策略。

MicroRNA-Directed Neuronal Reprogramming as a Therapeutic Strategy for Neurological Diseases.

机构信息

Dino Ferrari Centre, Neuroscience Section, Department of Pathophysiology and Transplantation (DEPT), Neurology Unit, IRCCS Foundation Ca' Granda Ospedale Maggiore Policlinico, University of Milan, Via Francesco Sforza 35, 20122, Milan, Italy.

出版信息

Mol Neurobiol. 2018 May;55(5):4428-4436. doi: 10.1007/s12035-017-0671-7. Epub 2017 Jun 29.

Abstract

The loss of neurons due to injury and disease results in a wide spectrum of highly disabling neurological and neurodegenerative conditions, given the apparent limited capacity of endogenous repair of the adult central nervous system (CNS). Therefore, it is important to develop technologies that can promote de novo neural stem cell and neuron generation. Current insights in CNS development and cellular reprogramming have provided the knowledge to finely modulate lineage-restricted transcription factors and microRNAs (miRNA) to elicit correct neurogenesis. Here, we discuss the current knowledge on the direct reprogramming of somatic non-neuronal cells into neural stem cells or subtype specific neurons in vitro and in vivo focusing on miRNA driven reprogramming. miRNA can allow rapid and efficient direct phenotype conversion by modulating gene networks active during development, which promote global shifts in the epigenetic landscape pivoting cell fate decisions. Furthermore, we critically present state-of-the-art and recent advances on miRNA therapeutics that can be applied to the diseased CNS. Together, the advances in our understanding of miRNA role in CNS development and disease, recent progress in miRNA-based therapeutic strategies, and innovative drug delivery methods create novel perspectives for meaningful therapies for neurodegenerative disorders.

摘要

由于损伤和疾病导致神经元的丧失,导致了广泛的高度致残的神经和神经退行性疾病,鉴于成人中枢神经系统(CNS)的内源性修复能力明显有限。因此,开发能够促进新的神经干细胞和神经元生成的技术非常重要。目前对 CNS 发育和细胞重编程的深入了解提供了知识,可精细调节谱系限制转录因子和 microRNA(miRNA)以引发正确的神经发生。在这里,我们讨论了当前关于体外和体内将体非神经元细胞直接重编程为神经干细胞或亚型特异性神经元的知识,重点是 miRNA 驱动的重编程。miRNA 可以通过调节发育过程中活跃的基因网络来快速有效地进行直接表型转换,从而推动表观遗传景观的全局转变,从而改变细胞命运决定。此外,我们还批判性地介绍了 miRNA 治疗学的最新进展,该治疗学可应用于患病的 CNS。总之,我们对 miRNA 在 CNS 发育和疾病中的作用的理解的进展,基于 miRNA 的治疗策略的最新进展以及创新的药物输送方法为神经退行性疾病的有意义治疗创造了新的视角。

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