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干细胞的代谢编程

The metabolic programming of stem cells.

作者信息

Shyh-Chang Ng, Ng Huck-Hui

机构信息

Genome Institute of Singapore, Singapore 138675.

出版信息

Genes Dev. 2017 Feb 15;31(4):336-346. doi: 10.1101/gad.293167.116. Epub 2017 Mar 17.

DOI:10.1101/gad.293167.116
PMID:28314766
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5358754/
Abstract

Advances in metabolomics have deepened our understanding of the roles that specific modes of metabolism play in programming stem cell fates. Here, we review recent metabolomic studies of stem cell metabolism that have revealed how metabolic pathways can convey changes in the extrinsic environment or their niche to program stem cell fates. The metabolic programming of stem cells represents a fine balance between the intrinsic needs of a cellular state and the constraints imposed by extrinsic conditions. A more complete understanding of these needs and constraints will afford us greater mastery over our control of stem cell fates.

摘要

代谢组学的进展加深了我们对特定代谢模式在干细胞命运编程中所起作用的理解。在此,我们回顾了近期关于干细胞代谢的代谢组学研究,这些研究揭示了代谢途径如何将外在环境或其生态位的变化传递给干细胞命运编程。干细胞的代谢编程代表了细胞状态的内在需求与外在条件所施加的限制之间的精细平衡。对这些需求和限制有更全面的理解将使我们在控制干细胞命运方面拥有更大的掌控力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/52c7/5358754/5cbb9bc90971/336f03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/52c7/5358754/1a309c4eb539/336f01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/52c7/5358754/df9d39829353/336f02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/52c7/5358754/5cbb9bc90971/336f03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/52c7/5358754/1a309c4eb539/336f01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/52c7/5358754/df9d39829353/336f02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/52c7/5358754/5cbb9bc90971/336f03.jpg

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Self-renewal of a purified Tie2+ hematopoietic stem cell population relies on mitochondrial clearance.纯化的Tie2+造血干细胞群体的自我更新依赖于线粒体清除。
Science. 2016 Dec 2;354(6316):1156-1160. doi: 10.1126/science.aaf5530. Epub 2016 Oct 13.
2
Specification of haematopoietic stem cell fate via modulation of mitochondrial activity.通过调节线粒体活性来规范造血干细胞命运。
Nat Commun. 2016 Oct 12;7:13125. doi: 10.1038/ncomms13125.
3
Glycolytic Metabolism Plays a Functional Role in Regulating Human Pluripotent Stem Cell State.
来自大鼠两个解剖部位的脂肪间充质干细胞的比较心肌细胞分化潜能:代谢组学分析与通路分析
Front Cell Dev Biol. 2025 Jun 19;13:1604605. doi: 10.3389/fcell.2025.1604605. eCollection 2025.
4
Dynamic Interplay Between Autophagy and Oxidative Stress in Stem Cells: Implications for Regenerative Medicine.干细胞中自噬与氧化应激之间的动态相互作用:对再生医学的启示
Antioxidants (Basel). 2025 Jun 6;14(6):691. doi: 10.3390/antiox14060691.
5
Enhanced glucose metabolism in Tet-deficient mouse embryonic stem cells.Tet 缺陷型小鼠胚胎干细胞中增强的葡萄糖代谢
Front Epigenet Epigenom. 2024;2. doi: 10.3389/freae.2024.1245823. Epub 2024 May 6.
6
Glycolytic activity instructs germ layer proportions through regulation of Nodal and Wnt signaling.糖酵解活性通过调控Nodal和Wnt信号传导来决定胚层比例。
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Stem Cell Res Ther. 2025 Apr 15;16(1):179. doi: 10.1186/s13287-025-04308-3.
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糖酵解代谢在调节人类多能干细胞状态中发挥功能性作用。
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