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DNA damage and toxicogenomic analyses of hydrogen sulfide in human intestinal epithelial FHs 74 Int cells
Author(s) -
AtteneRamos Matias S.,
Nava Gerardo M.,
Muellner Mark G.,
Wagner Elizabeth D.,
Plewa Michael J.,
Gaskins H. Rex
Publication year - 2010
Publication title -
environmental and molecular mutagenesis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1
H-Index - 87
eISSN - 1098-2280
pISSN - 0893-6692
DOI - 10.1002/em.20546
Subject(s) - genotoxicity , comet assay , biology , dna damage , mutagen , microbiology and biotechnology , dna repair , intestinal epithelium , gene expression , downregulation and upregulation , gene , carcinogen , toxicity , dna , biochemistry , chemistry , genetics , epithelium , organic chemistry
Hydrogen sulfide (H 2 S), a metabolic end product of sulfate‐reducing bacteria, represents a genotoxic insult to the colonic epithelium, which may also be linked with chronic disorders such as ulcerative colitis and colorectal cancer. This study defined the early (30 min) and late (4 hr) response of nontransformed human intestinal epithelial cells (FHs 74 Int) to H 2 S. The genotoxicity of H 2 S was measured using the single‐cell gel electrophoresis (comet) assay. Changes in gene expression were analyzed after exposure to a genotoxic, but not cytotoxic, concentration of H 2 S (500 μM H 2 S) using pathway‐specific quantitative RT‐PCR gene arrays. H 2 S was genotoxic in a concentration range from 250 to 2,000 μM, which is similar to concentrations found in the large intestine. Significant changes in gene expression were predominantly observed at 4 hr, with the greatest responses by PTGS2 ( COX‐2 ; 7.92‐fold upregulated) and WNT2 (7.08‐fold downregulated). COX‐2 was the only gene upregulated at both 30 min and 4 hr. Overall, the study demonstrates that H 2 S modulates the expression of genes involved in cell‐cycle progression and triggers both inflammatory and DNA repair responses. This study confirms the genotoxic properties of H 2 S in nontransformed human intestinal epithelial cells and identifies functional pathways by which this bacterial metabolite may perturb cellular homeostasis and contribute to the onset of chronic intestinal disorders. Environ. Mol. Mutagen. 2010. © 2010 Wiley‐Liss, Inc.