增强溶酶体激活恢复衰老过程中的神经干细胞功能。

Journal of Experimental Neuroscience Pub Date : 2018-08-23 eCollection Date: 2018-01-01 DOI:10.1177/1179069518795874
Amanda J Audesse, Ashley E Webb
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引用次数: 8

摘要

成年神经发生支持哺乳动物的认知和感觉功能,并随着年龄的增长而显著减少。静止的神经干细胞是成年大脑中新神经元的来源,新出现的证据表明,这些细胞无法激活并重新进入细胞周期是老年动物神经发生减少的主要原因。然而,在成人和老年大脑中支持静止和激活的分子机制仍然不清楚。Leeman等人最近发表在《科学》杂志上的研究揭示了溶酶体在支持神经干细胞激活中的新作用,并揭示了衰老过程中溶酶体功能的丧失导致神经干细胞活性降低。结合转录组学和功能分析,作者发现静止和激活的神经干细胞使用不同的蛋白质静止网络分支,静止的干细胞特别依赖于溶酶体自噬系统。令人兴奋的是,在老年静止人群中刺激溶酶体活性显著增强了他们激活神经干细胞和祖细胞的能力,并增加了神经干细胞生态位内激活神经干细胞和祖细胞的频率。这项工作首次确定了溶酶体功能障碍是衰老过程中神经发生减少的原因,并表明增强溶酶体功能足以恢复衰老大脑中健康的干细胞活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Enhancing Lysosomal Activation Restores Neural Stem Cell Function During Aging.

Enhancing Lysosomal Activation Restores Neural Stem Cell Function During Aging.

Enhancing Lysosomal Activation Restores Neural Stem Cell Function During Aging.

Adult neurogenesis supports cognitive and sensory functions in mammals and is significantly reduced with age. Quiescent neural stem cells are the source of new neurons in the adult brain and emerging evidence suggests that the failure of these cells to activate and re-enter the cell cycle is largely responsible for reduced neurogenesis in old animals. However, the molecular mechanisms supporting quiescence and activation in the adult and aged brain remain undefined. Recent work published by Leeman et al. in Science uncovers a novel role for lysosomes in supporting neural stem cell activation, and reveals that loss of lysosome function during aging contributes to reduced neural stem cell activity. Using a combination of transcriptomics and functional analysis, the authors show that quiescent and activated neural stem cells employ different branches of proteostasis networks, with quiescent stem cells particularly dependent on the lysosome-autophagy system. Excitingly, stimulation of lysosomal activity in the aged quiescent population significantly enhanced their ability to activate and increased the frequency of activated neural stem and progenitor cells within the neural stem cell niche. This work for the first time identifies lysosomal dysfunction as a cause of reduced neurogenesis during aging, and shows that enhancing lysosomal function is sufficient to restore healthy stem cell activity in the aged brain.

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