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IDO1 Maintains Pluripotency of Primed Human Embryonic Stem Cells by Promoting Glycolysis

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机构: [1]Center for Regenerative and Translational Medicine, Guangdong Provincial Academy of Chinese Medical Sciences, The Second Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou, Guangdong, People’s Republic of China [2]Division of Biological Sciences, University of California, San Diego, La Jolla, California, USA [3]The Eighth Affiliated Hospital, Sun Yat-sen University, Shenzhen, Guangdong, People’s Republic of China
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关键词: Human embryonic stem cells Pluripotency Differentiation Glycolysis Oxidative phosphorylation

摘要:
Human embryonic stem cells (hESCs) depend on glycolysis for energy supply and pluripotency and switch to oxidative phosphorylation upon differentiation. The underlying mechanisms remain unclear. Here, we demonstrate that indoleamine 2,3-dioxygenase 1 (IDO1) is expressed in primed hESCs and its expression rapidly downregulated upon hESC differentiation. IDO1 is required to maintain pluripotency by suppressing mitochondria activity and promoting glycolysis through the increase of NAD(+)/NADH ratio. The upregulation of IDO1 during hESC differentiation suppresses the differentiation of hESCs into certain lineages of cells such as cardiomyocytes, which depend on oxidative phosphorylation to satisfy their high energy demand. Therefore, IDO1 plays important roles in maintaining the pluripotency of hESCs. Stem Cells 2019;37:1158-1165

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出版当年[2018]版:
大类 | 2 区 医学
小类 | 2 区 生物工程与应用微生物 2 区 细胞与组织工程 2 区 细胞生物学 2 区 血液学 2 区 肿瘤学
最新[2025]版:
大类 | 3 区 医学
小类 | 2 区 生物工程与应用微生物 3 区 细胞与组织工程 3 区 细胞生物学 3 区 血液学 3 区 肿瘤学
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出版当年[2017]版:
Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Q1 CELL & TISSUE ENGINEERING Q1 CELL BIOLOGY Q1 ONCOLOGY Q1 HEMATOLOGY
最新[2023]版:
Q1 HEMATOLOGY Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Q2 CELL & TISSUE ENGINEERING Q2 CELL BIOLOGY Q2 ONCOLOGY

影响因子: 最新[2023版] 最新五年平均 出版当年[2017版] 出版当年五年平均 出版前一年[2016版] 出版后一年[2018版]

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第一作者机构: [1]Center for Regenerative and Translational Medicine, Guangdong Provincial Academy of Chinese Medical Sciences, The Second Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou, Guangdong, People’s Republic of China [2]Division of Biological Sciences, University of California, San Diego, La Jolla, California, USA
通讯作者:
通讯机构: [1]Center for Regenerative and Translational Medicine, Guangdong Provincial Academy of Chinese Medical Sciences, The Second Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou, Guangdong, People’s Republic of China [2]Division of Biological Sciences, University of California, San Diego, La Jolla, California, USA [3]The Eighth Affiliated Hospital, Sun Yat-sen University, Shenzhen, Guangdong, People’s Republic of China [*1]The Eighth Affiliated Hospital, Sun Yat-sen University, Shenzhen 518033, Guangdong, People’s Republic of China. [*2]Center for Regenerative and Translational Medicine, Guangdong Provincial Academy of Chinese Medical Sciences, The Second Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou 510632, Guangdong, People’s Republic of China.
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