Mitochondrial Metabolism-Mediated Regulation of Adult Neurogenesis.

Ruth Beckervordersandforth
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引用次数: 63

Abstract

The life-long generation of new neurons from radial glia-like neural stem cells (NSCs) is achieved through a stereotypic developmental sequence that requires precise regulatory mechanisms to prevent exhaustion or uncontrolled growth of the stem cell pool. Cellular metabolism is the new kid on the block of adult neurogenesis research and the identity of stage-specific metabolic programs and their impact on neurogenesis turns out to be an emerging research topic in the field. Mitochondrial metabolism is best known for energy production but it contains a great deal more. Mitochondria are key players in a variety of cellular processes including ATP synthesis through functional coupling of the electron transport chain and oxidative phosphorylation, recycling of hydrogen carriers, biosynthesis of cellular building blocks, and generation of reactive oxygen species that can modulate signaling pathways in a redox-dependent fashion. In this review, I will discuss recent findings describing stage-specific modulations of mitochondrial metabolism within the adult NSC lineage, emphasizing its importance for NSC self-renewal, proliferation of neural stem and progenitor cells (NSPCs), cell fate decisions, and differentiation and maturation of newborn neurons. I will furthermore summarize the important role of mitochondrial dysfunction in tissue regeneration and ageing, suggesting it as a potential therapeutic target for regenerative medicine practice.

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线粒体代谢介导的成人神经发生调控。
放射状胶质样神经干细胞(NSCs)的新神经元的终身生成是通过一个刻板的发育序列实现的,该序列需要精确的调节机制来防止干细胞库的耗尽或不受控制的生长。细胞代谢是成人神经发生研究的新生事物,而阶段特异性代谢程序的识别及其对神经发生的影响已成为该领域的新兴研究课题。线粒体代谢最为人所知的是产生能量,但它包含的远不止这些。线粒体是多种细胞过程的关键参与者,包括通过电子传递链和氧化磷酸化的功能偶联合成ATP,氢载体的再循环,细胞构建块的生物合成,以及可以以氧化还原依赖的方式调节信号通路的活性氧的产生。在这篇综述中,我将讨论最近的研究结果,描述成年NSC谱系中线粒体代谢的阶段特异性调节,强调其对NSC自我更新、神经干细胞和祖细胞(NSPCs)的增殖、细胞命运决定以及新生神经元的分化和成熟的重要性。我将进一步总结线粒体功能障碍在组织再生和衰老中的重要作用,并建议它作为再生医学实践的潜在治疗靶点。
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