生物
诱导多能干细胞
重编程
干细胞
细胞生物学
胚胎干细胞
遗传学
细胞
基因
作者
Liang Yue,Yangli Pei,Zhong Liu,Henry Yang,Yanliang Wang,Wei Zhang,Naixin Chen,Qianqian Zhu,Jie Gao,Minglei Zhi,Bingqiang Wen,Shaopeng Zhang,Jinzhu Xiang,Qingqing Wei,Hui Liu,Suying Cao,Huiqiang Lou,Zhongzhou Chen,Jianyong Han
标识
DOI:10.1016/j.stemcr.2020.06.018
摘要
Summary
The pluripotency of stem cells determines their developmental potential. While the pluripotency states of pluripotent stem cells are variable and interconvertible, the mechanisms underlying the acquisition and maintenance of pluripotency remain largely elusive. Here, we identified that methylenetetrahydrofolate dehydrogenase (NAD+-dependent), methenyltetrahydrofolate cyclohydrolase (Mthfd2) plays an essential role in maintaining embryonic stem cell pluripotency and promoting complete reprogramming of induced pluripotent stem cells. Mechanistically, in mitochondria, Mthfd2 maintains the integrity of the mitochondrial respiratory chain and prevents mitochondrial dysfunction. In the nucleus, Mthfd2 stabilizes the phosphorylation of EXO1 to support DNA end resection and promote homologous recombination repair. Our results revealed that Mthfd2 is a dual-function factor in determining the pluripotency of pluripotent stem cells through both mitochondrial and nuclear pathways, ultimately ensuring safe application of pluripotent stem cells.
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