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本文引用的文献

1
Metabolic regulation of cell growth and proliferation.细胞生长和增殖的代谢调控。
Nat Rev Mol Cell Biol. 2019 Jul;20(7):436-450. doi: 10.1038/s41580-019-0123-5.
2
Glutamine Metabolism Regulates Proliferation and Lineage Allocation in Skeletal Stem Cells.谷氨酰胺代谢调节骨骼干细胞的增殖和谱系分配。
Cell Metab. 2019 Apr 2;29(4):966-978.e4. doi: 10.1016/j.cmet.2019.01.016. Epub 2019 Feb 14.
3
Mitochondrial Stress-Initiated Aberrant Activation of the NLRP3 Inflammasome Regulates the Functional Deterioration of Hematopoietic Stem Cell Aging.线粒体应激引发 NLRP3 炎性小体的异常激活调控造血干细胞衰老功能恶化。
Cell Rep. 2019 Jan 22;26(4):945-954.e4. doi: 10.1016/j.celrep.2018.12.101.
4
Fueling the Cycle: CDKs in Carbon and Energy Metabolism.推动循环:细胞周期蛋白依赖性激酶在碳代谢和能量代谢中的作用
Front Cell Dev Biol. 2018 Aug 17;6:93. doi: 10.3389/fcell.2018.00093. eCollection 2018.
5
Distinct metabolic states govern skeletal muscle stem cell fates during prenatal and postnatal myogenesis.不同的代谢状态在胚胎期和出生后肌肉发生过程中控制着骨骼肌干细胞的命运。
J Cell Sci. 2018 Jul 27;131(14):jcs212977. doi: 10.1242/jcs.212977.
6
Mapping Metabolism: Monitoring Lactate Dehydrogenase Activity Directly in Tissue.代谢图谱:直接监测组织中的乳酸脱氢酶活性
J Vis Exp. 2018 Jun 21(136):57760. doi: 10.3791/57760.
7
Fasting Activates Fatty Acid Oxidation to Enhance Intestinal Stem Cell Function during Homeostasis and Aging.禁食激活脂肪酸氧化以增强稳态和衰老过程中的肠道干细胞功能。
Cell Stem Cell. 2018 May 3;22(5):769-778.e4. doi: 10.1016/j.stem.2018.04.001.
8
Metabolic Maturation during Muscle Stem Cell Differentiation Is Achieved by miR-1/133a-Mediated Inhibition of the Dlk1-Dio3 Mega Gene Cluster.代谢成熟在肌肉干细胞分化过程中是通过 miR-1/133a 介导的 Dlk1-Dio3 Mega 基因簇的抑制来实现的。
Cell Metab. 2018 May 1;27(5):1026-1039.e6. doi: 10.1016/j.cmet.2018.02.022. Epub 2018 Apr 5.
9
Waking up muscle stem cells: PI3K signalling is ringing.唤醒肌肉干细胞:PI3K 信号正在响起。
EMBO J. 2018 Apr 13;37(8). doi: 10.15252/embj.201899297. Epub 2018 Mar 26.
10
A Fatty Acid Oxidation-Dependent Metabolic Shift Regulates Adult Neural Stem Cell Activity.脂肪酸氧化依赖性代谢转变调节成体神经干细胞活性。
Cell Rep. 2017 Aug 29;20(9):2144-2155. doi: 10.1016/j.celrep.2017.08.029.

静止干细胞代谢的悖论。

The paradox of metabolism in quiescent stem cells.

机构信息

Department of Molecular, Cell and Developmental Biology, University of California, Los Angeles, CA, USA.

Department of Biological Chemistry, David Geffen School of Medicine, Los Angeles, CA, USA.

出版信息

FEBS Lett. 2019 Oct;593(20):2817-2839. doi: 10.1002/1873-3468.13608. Epub 2019 Sep 27.

DOI:10.1002/1873-3468.13608
PMID:31531979
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7034665/
Abstract

The shift between a proliferating and a nonproliferating state is associated with significant changes in metabolic needs. Proliferating cells tend to have higher metabolic rates, and their metabolic profiles facilitate biosynthesis, as compared to those of nondividing cells of the same sort. Recent studies have elucidated specific molecules that control metabolic changes while cells shift between proliferation and quiescence. Embryonic stem cells, which are rapidly proliferating, tend to have metabolic patterns that are similar to those of nonstem cells in a proliferative state. Moreover, although adult stem cells tend to be quiescent, their metabolic profiles have been reported in multiple organs to more closely resemble those of proliferating than those of nondividing cells in some respects. The findings raise questions about whether there are metabolic profiles that are required for stemness, and whether these profiles relate to the metabolic properties that may be required for quiescence. Here, we review the literature on how metabolism changes upon commitment to proliferation and compare the proliferating and nonproliferating metabolic states of differentiated cells and embryonic and adult stem cells.

摘要

细胞由增殖状态向非增殖状态的转变与代谢需求的显著变化有关。与同类型的非分裂细胞相比,增殖细胞往往具有更高的代谢率,其代谢特征有利于生物合成。最近的研究阐明了特定的分子,这些分子在细胞增殖和静止之间转换时控制代谢变化。快速增殖的胚胎干细胞往往具有与增殖状态下的非干细胞相似的代谢模式。此外,尽管成体干细胞通常处于静止状态,但在多个器官中已经报道了它们的代谢特征在某些方面更类似于增殖细胞而不是非分裂细胞。这些发现提出了这样的问题,即是否存在维持干细胞特性所需的代谢特征,以及这些特征是否与静止所需的代谢特性有关。在这里,我们综述了关于细胞向增殖状态转变时代谢变化的文献,并比较了分化细胞、胚胎干细胞和成体干细胞的增殖和非增殖代谢状态。