硫芥对增殖干细胞DNA损伤的影响

IF 2.6 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY DNA and cell biology Pub Date : 2022-08-01 Epub Date: 2022-07-13 DOI:10.1089/dna.2022.0073
Zengming Zhao, Xiabei Yan, Lizhong Li, Yulei Shu, Jun He, Lili Wang, Qingzhen Huang, Jianwei Xie, Jun Zhao, Shuangqing Peng
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引用次数: 2

摘要

硫磺芥(SM)是一种化学战剂,可以与DNA、RNA和蛋白质形成加合物。与DNA的反应导致DNA单加合物和链间交联的形成,导致DNA损伤,是SM毒性的重要组成部分。我们之前的体内研究表明,分裂细胞如造血干细胞和肠绒毛干细胞似乎对SM的敏感性增加。因此,为了比较体细胞和干细胞对SM的敏感性和SM细胞毒性的机制,我们分离了人包皮成纤维细胞,将其重编程为多能干细胞,然后比较SM处理所涉及的DNA损伤修复途径。我们的研究结果表明,增殖干细胞对sm诱导的DNA损伤更敏感,损伤主要包括单链断裂。此外,干细胞和体细胞参与DNA修复的途径是不同的。
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Proliferating Stem Cells are Acutely Affected by DNA Damage Induced by Sulfur Mustard.

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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来源期刊
DNA and cell biology
DNA and cell biology 生物-生化与分子生物学
CiteScore
6.60
自引率
0.00%
发文量
93
审稿时长
1.5 months
期刊介绍: DNA and Cell Biology delivers authoritative, peer-reviewed research on all aspects of molecular and cellular biology, with a unique focus on combining mechanistic and clinical studies to drive the field forward. DNA and Cell Biology coverage includes: Gene Structure, Function, and Regulation Gene regulation Molecular mechanisms of cell activation Mechanisms of transcriptional, translational, or epigenetic control of gene expression Molecular Medicine Molecular pathogenesis Genetic approaches to cancer and autoimmune diseases Translational studies in cell and molecular biology Cellular Organelles Autophagy Apoptosis P bodies Peroxisosomes Protein Biosynthesis and Degradation Regulation of protein synthesis Post-translational modifications Control of degradation Cell-Autonomous Inflammation and Host Cell Response to Infection Responses to cytokines and other physiological mediators Evasive pathways of pathogens.
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