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本文引用的文献

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Metabolic control of adult neural stem cell activity by Fasn-dependent lipogenesis.Fasn 依赖性脂生成对成体神经干细胞活性的代谢控制。
Nature. 2013 Jan 10;493(7431):226-30. doi: 10.1038/nature11689. Epub 2012 Dec 2.
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Influence of threonine metabolism on S-adenosylmethionine and histone methylation.苏氨酸代谢对 S-腺苷甲硫氨酸和组蛋白甲基化的影响。
Science. 2013 Jan 11;339(6116):222-6. doi: 10.1126/science.1226603. Epub 2012 Nov 1.
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Increased proteasome activity in human embryonic stem cells is regulated by PSMD11.人胚胎干细胞中蛋白酶体活性的增加受 PSMD11 调节。
Nature. 2012 Sep 13;489(7415):304-8. doi: 10.1038/nature11468.
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mTOR complex 1 plays critical roles in hematopoiesis and Pten-loss-evoked leukemogenesis.mTOR 复合物 1 在造血和 Pten 缺失诱导的白血病发生中发挥关键作用。
Cell Stem Cell. 2012 Sep 7;11(3):429-39. doi: 10.1016/j.stem.2012.06.009.
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A PML–PPAR-δ pathway for fatty acid oxidation regulates hematopoietic stem cell maintenance.脂肪酸氧化的 PML–PPAR-δ 通路调节造血干细胞维持。
Nat Med. 2012 Sep;18(9):1350-8. doi: 10.1038/nm.2882.
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mTORC1 in the Paneth cell niche couples intestinal stem-cell function to calorie intake.mTORC1 在潘氏细胞龛中将肠干细胞功能与热量摄入联系起来。
Nature. 2012 Jun 28;486(7404):490-5. doi: 10.1038/nature11163.
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SIRT1 is required for AMPK activation and the beneficial effects of resveratrol on mitochondrial function.SIRT1 对于 AMPK 的激活以及白藜芦醇对线粒体功能的有益作用是必需的。
Cell Metab. 2012 May 2;15(5):675-90. doi: 10.1016/j.cmet.2012.04.003.
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mTOR signaling in growth control and disease.mTOR 信号在生长控制和疾病中的作用。
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An elaborate regulation of Mammalian target of rapamycin activity is required for somatic cell reprogramming induced by defined transcription factors.哺乳动物雷帕霉素靶蛋白活性的精细调控对于由特定转录因子诱导的体细胞重编程是必需的。
Stem Cells Dev. 2012 Sep 20;21(14):2630-41. doi: 10.1089/scd.2012.0015. Epub 2012 May 17.
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HIF1α induced switch from bivalent to exclusively glycolytic metabolism during ESC-to-EpiSC/hESC transition.HIF1α 诱导 ESC 向 EpiSC/hESC 过渡过程中从二价状态到完全糖酵解代谢的转变。
EMBO J. 2012 May 2;31(9):2103-16. doi: 10.1038/emboj.2012.71. Epub 2012 Mar 23.

哺乳动物胚胎和成年干细胞命运中的能量代谢和能量感应途径。

Energy metabolism and energy-sensing pathways in mammalian embryonic and adult stem cell fate.

机构信息

Department of Genetics, Stanford University, Stanford, CA 94305, USA.

出版信息

J Cell Sci. 2012 Dec 1;125(Pt 23):5597-608. doi: 10.1242/jcs.114827.

DOI:10.1242/jcs.114827
PMID:23420198
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3575699/
Abstract

Metabolism is influenced by age, food intake, and conditions such as diabetes and obesity. How do physiological or pathological metabolic changes influence stem cells, which are crucial for tissue homeostasis? This Commentary reviews recent evidence that stem cells have different metabolic demands than differentiated cells, and that the molecular mechanisms that control stem cell self-renewal and differentiation are functionally connected to the metabolic state of the cell and the surrounding stem cell niche. Furthermore, we present how energy-sensing signaling molecules and metabolism regulators are implicated in the regulation of stem cell self-renewal and differentiation. Finally, we discuss the emerging literature on the metabolism of induced pluripotent stem cells and how manipulating metabolic pathways might aid cellular reprogramming. Determining how energy metabolism regulates stem cell fate should shed light on the decline in tissue regeneration that occurs during aging and facilitate the development of therapies for degenerative or metabolic diseases.

摘要

新陈代谢受年龄、饮食以及糖尿病和肥胖等疾病的影响。生理或病理代谢变化如何影响干细胞,干细胞对于组织稳态至关重要?本述评综述了最近的证据,表明干细胞比分化细胞有不同的代谢需求,并且控制干细胞自我更新和分化的分子机制与细胞的代谢状态以及周围的干细胞龛功能相关。此外,我们还介绍了能量感应信号分子和代谢调节剂如何参与干细胞自我更新和分化的调控。最后,我们讨论了诱导多能干细胞代谢的新兴文献,以及操纵代谢途径如何有助于细胞重编程。确定能量代谢如何调节干细胞命运,应该能够阐明衰老过程中组织再生能力下降的原因,并促进退行性或代谢性疾病治疗方法的发展。