Suppr超能文献

从成熟胶质细胞中制造神经元:一个牵强的梦想?

Making neurons from mature glia: a far-fetched dream?

机构信息

Institute for Stem Cell Research, National Research Center for Environment and Health, Ingolstädter Landstrasse 1, D-85764 Neuherberg, Germany.

出版信息

Neuropharmacology. 2010 May;58(6):894-902. doi: 10.1016/j.neuropharm.2009.11.004. Epub 2009 Nov 18.

Abstract

The fact that cells with glial characteristics such as forebrain radial glia during development and astroglial stem cells in the adult neurogenic zones serve as neuronal precursors provokes the question why glia in most other areas of the adult central nervous system are apparently incapable of generating new neurons. Besides being of pivotal biological interest answers to this question may also open new avenues for cell-based therapies of neurodegenerative diseases that involve a permanent loss of neurons which are not replaced naturally. For if one could indeed instruct glia to generate neurons, such a strategy would carry the enormous advantage of making use of a large pool of endogenous, and hence autologous cells, thereby circumventing many of the problems associated with therapeutic strategies based on transplantation. Accordingly, the recent years have seen increasing effort in assessing the plasticity of astroglia and other types of resident non-neuronal cells as a potential source for new neurons in the injured brain or eye. For instance, following injury astroglia in the cerebral cortex and Müller glia in the retina can de-differentiate and acquire stem or precursor cell like properties. Moreover, it has been shown that astroglia can be reprogrammed in vitro by forced expression of neurogenic transcription factors to transgress their lineage restriction and stably acquire a neuronal identity. In this review I will discuss the status quo of these early attempts, the limitations currently encountered and the future challenges before the full potential of this approach can be weighed.

摘要

事实是,具有神经胶质特征的细胞,如发育中的前脑放射状胶质和成年神经发生区的星形胶质干细胞,可作为神经元前体,这引发了一个问题,即为什么成年中枢神经系统的大多数其他区域的胶质细胞显然不能产生新的神经元。除了具有重要的生物学意义外,对这个问题的回答也可能为基于细胞的神经退行性疾病的治疗开辟新途径,这些疾病涉及神经元的永久性丧失,而神经元不会自然替代。因为如果确实可以指示神经胶质产生神经元,那么这种策略将具有巨大的优势,即利用大量内源性的、因此是自体的细胞,从而避免了许多与基于移植的治疗策略相关的问题。因此,近年来,人们越来越努力地评估星形胶质细胞和其他类型的固有非神经元细胞的可塑性,作为受伤大脑或眼睛中新神经元的潜在来源。例如,在大脑皮质中,星形胶质细胞和视网膜中的 Müller 胶质细胞在受伤后可以去分化并获得干细胞或前体细胞样特性。此外,已经表明,星形胶质细胞可以通过强制表达神经发生转录因子在体外重编程,以跨越其谱系限制并稳定获得神经元特性。在这篇综述中,我将讨论这些早期尝试的现状、当前遇到的限制以及在充分发挥这种方法的潜力之前面临的未来挑战。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验