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促进内源性神经胶质细胞生成神经元的新兴药理学方法。

Emerging pharmacological approaches to promote neurogenesis from endogenous glial cells.

作者信息

Boda Enrica, Nato Giulia, Buffo Annalisa

机构信息

Department of Neuroscience Rita Levi-Montalcini, University of Turin, I-10126 Turin, Italy; Neuroscience Institute Cavalieri Ottolenghi, I-10043 Orbassano, Turin, Italy.

Department of Neuroscience Rita Levi-Montalcini, University of Turin, I-10126 Turin, Italy; Neuroscience Institute Cavalieri Ottolenghi, I-10043 Orbassano, Turin, Italy.

出版信息

Biochem Pharmacol. 2017 Oct 1;141:23-41. doi: 10.1016/j.bcp.2017.06.129. Epub 2017 Jun 22.

DOI:10.1016/j.bcp.2017.06.129
PMID:28647491
Abstract

Neurodegenerative disorders are emerging as leading contributors to the global disease burden. While some drug-based approaches have been designed to limit or prevent neuronal loss following acute damage or chronic neurodegeneration, regeneration of functional neurons in the adult Central Nervous System (CNS) still remains an unmet need. In this context, the exploitation of endogenous cell sources has recently gained an unprecedented attention, thanks to the demonstration that, in some CNS regions or under specific circumstances, glial cells can activate spontaneous neurogenesis or can be instructed to produce neurons in the adult mammalian CNS parenchyma. This field of research has greatly advanced in the last years and identified interesting molecular and cellular mechanisms guiding the neurogenic activation/conversion of glia. In this review, we summarize the evolution of the research devoted to understand how resident glia can be directed to produce neurons. We paid particular attention to pharmacologically-relevant approaches exploiting the modulation of niche-associated factors and the application of selected small molecules.

摘要

神经退行性疾病正逐渐成为全球疾病负担的主要成因。尽管已经设计了一些基于药物的方法来限制或预防急性损伤或慢性神经退行性变后的神经元丢失,但成体中枢神经系统(CNS)中功能性神经元的再生仍然是未被满足的需求。在这种背景下,由于有证据表明,在某些中枢神经系统区域或特定情况下,胶质细胞可以激活自发神经发生,或者可以被诱导在成年哺乳动物中枢神经系统实质中产生神经元,内源性细胞来源的开发最近受到了前所未有的关注。在过去几年中,该研究领域取得了很大进展,并确定了指导胶质细胞神经源性激活/转化的有趣分子和细胞机制。在这篇综述中,我们总结了致力于理解如何引导驻留胶质细胞产生神经元的研究进展。我们特别关注利用对生态位相关因子的调节以及应用选定小分子的药理学相关方法。

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Small molecules reprogram reactive astrocytes into neuronal cells in the injured adult spinal cord.小分子可将损伤成年脊髓中的反应性星形胶质细胞重编程为神经元细胞。
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