生物
干细胞
DNA损伤
DNA
诱导多能干细胞
细胞生物学
DNA修复
体细胞
造血
分子生物学
遗传学
基因
胚胎干细胞
作者
Zengming Zhao,Xiabei Yan,Lizhong Li,Yulei Shu,Jun He,Lili Wang,Huang Qing-zhen,Jianwei Xie,Jun Zhao,Shuangqing Peng
标识
DOI:10.1089/dna.2022.0073
摘要
Sulfur mustard (SM), a chemical warfare agent, can form adducts with DNA, RNA, and proteins. Reactions with DNA lead to the formation of both DNA monoadducts and interstrand cross-links, resulting in DNA damage, and is an important component of SM toxicity. Our previous in vivo studies indicated that dividing cells such as hematopoietic stem cells and intestinal villi stem cells seemed to have increased sensitivity to SM. Therefore, to compare the sensitivity of somatic and stem cells to SM and to investigate the mechanism of SM cytotoxicity, we isolated human foreskin fibroblasts, reprogrammed them into pluripotent stem cells, and then compared the DNA damage repair pathways involved upon SM treatment. Our results indicated that proliferating stem cells were more sensitive to SM-induced DNA damage, and the damage mainly comprised single-stranded breaks. Furthermore, the pathways involved in DNA repair in stem cells and somatic cells were different.
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