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成体脑室下区的神经干细胞氧化脂肪酸以产生能量并支持神经发生活动。

Neural Stem Cells in the Adult Subventricular Zone Oxidize Fatty Acids to Produce Energy and Support Neurogenic Activity.

作者信息

Stoll Elizabeth A, Makin Rebecca, Sweet Ian R, Trevelyan Andrew J, Miwa Satomi, Horner Philip J, Turnbull Douglass M

机构信息

Centre for Brain Ageing and Vitality, Newcastle University, Newcastle upon Tyne, United Kingdom.

Wellcome Trust Centre for Mitochondrial Research, Institute for Ageing and Health, Newcastle University, Newcastle upon Tyne, United Kingdom.

出版信息

Stem Cells. 2015 Jul;33(7):2306-19. doi: 10.1002/stem.2042. Epub 2015 Jun 4.

Abstract

Neural activity is tightly coupled to energy consumption, particularly sugars such as glucose. However, we find that, unlike mature neurons and astrocytes, neural stem/progenitor cells (NSPCs) do not require glucose to sustain aerobic respiration. NSPCs within the adult subventricular zone (SVZ) express enzymes required for fatty acid oxidation and show sustained increases in oxygen consumption upon treatment with a polyunsaturated fatty acid. NSPCs also demonstrate sustained decreases in oxygen consumption upon treatment with etomoxir, an inhibitor of fatty acid oxidation. In addition, etomoxir decreases the proliferation of SVZ NSPCs without affecting cellular survival. Finally, higher levels of neurogenesis can be achieved in aged mice by ectopically expressing proliferator-activated receptor gamma coactivator 1 alpha (PGC1α), a factor that increases cellular aerobic capacity by promoting mitochondrial biogenesis and metabolic gene transcription. Regulation of metabolic fuel availability could prove a powerful tool in promoting or limiting cellular proliferation in the central nervous system. Stem Cells 2015;33:2306-2319.

摘要

神经活动与能量消耗紧密相关,尤其是与葡萄糖等糖类。然而,我们发现,与成熟神经元和星形胶质细胞不同,神经干/祖细胞(NSPCs)并不需要葡萄糖来维持有氧呼吸。成年脑室下区(SVZ)内的NSPCs表达脂肪酸氧化所需的酶,在用多不饱和脂肪酸处理后,其耗氧量持续增加。在用脂肪酸氧化抑制剂依托莫昔处理后,NSPCs的耗氧量也会持续下降。此外,依托莫昔会降低SVZ NSPCs的增殖,但不影响细胞存活。最后,通过异位表达增殖激活受体γ辅激活因子1α(PGC1α),可在衰老小鼠中实现更高水平的神经发生,PGC1α是一种通过促进线粒体生物发生和代谢基因转录来提高细胞有氧能力的因子。调节代谢燃料的可用性可能是促进或限制中枢神经系统细胞增殖的有力工具。《干细胞》2015年;33:2306 - 2319。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/303b/4834818/d435be9a79bd/STEM-33-2306-g001.jpg

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