表观遗传学
组蛋白
DNA甲基化
甲基化
乙酰化
组蛋白H3
生物
组蛋白甲基化
DNA
硫芥
遗传学
分子生物学
细胞生物学
化学
基因
基因表达
毒性
有机化学
作者
Thilo Simons,Dirk Steinritz,Birgit Bölck,Annette Schmidt,Tanja Popp,Horst Thiermann,Thomas Gudermann,Wilhelm Bloch,Kai Kehe
标识
DOI:10.1016/j.toxlet.2017.11.010
摘要
The chemical warfare agent sulfur mustard (SM) can cause long-term health effects that may occur even years after a single exposure. The underlying pathophysiology is unknown, but epigenetic mechanisms are discussed as feasible explanation. "Epigenetics" depicts regulation of gene function without affecting the DNA sequence itself. DNA-methylation and covalent histone modifications (methylation or acetylation) are regarded as important processes. In the present in vitro study using early endothelial cells (EEC), we analyzed SM-induced DNA methylation over time and compared results to an in vivo skin sample that was obtained approx. one year after an accidental SM exposure. EEC were exposed to low SM concentrations (0.5 and 1.0μM). DNA methylation and histone acetylation (H3-K9, H3-K27, H4-K8) or histone di-methylation (H3-K9, H3-K27, H3-K36) were investigated 24h after exposure, and after 2 or 4 additional cell passages. The human skin sample was assessed in parallel. SM had only some minor effects on histone modifications. However, a significant and pronounced increase of DNA methylation was detected in the late cell passages as well as in the skin sample. Our results indicate that SM does indeed cause epigenetic modifications that appear to persist over time.
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