Abstract
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 1.0 μM).
DNA methylation and histone acetylation (H3-K9, H3-K27, H4-K8) or
histone di-methylation (H3-K9, H3-K27, H3-K36) were investigated 24 h
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.
Originalsprache | Englisch |
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Zeitschrift | Toxicology letters |
Jahrgang | 293 |
Seiten (von - bis) | 45-50 |
Seitenumfang | 6 |
ISSN | 0378-4274 |
DOIs | |
Publikationsstatus | Veröffentlicht - 01.09.2018 |