2004Toxicology Mechanisms and MethodsRequires access

Cross-Linking Interferes with Assessing Sulfur Mustard-Induced DNA Damage in Human Peripheral Blood Lymphocytes Using the Comet Assay

Janet Moser, Claire F. Levine, Delvena R. Thomas-Dunmeyer, William J. Smith

Open publisher page 11 citations

Abstract

Sulfur mustard (SM) is a blistering agent that produces DNA strand breaks. To detect SM-induced DNA single strand breaks in human peripheral blood lymphocytes (PBL), cells were exposed to various concentrations of SM (10 to 1000 muM), and the comet assay (single-cell gel electrophoresis) was performed. We observed a SM concentration- and time-dependent increase in detectable DNA damage. To test whether SM-induced DNA cross-linking inhibits DNA migration in the comet assay, PBL were exposed to a) SM alone (10 to 1000 muM), b) H(2)O(2) (0.001%), which produces DNA single strand breaks with no cross-links, or c) SM followed at 2, 4, or 6 h by H(2)O(2). With H(2)O(2) alone, a large amount of strand breakage was detected. With H(2)O(2) plus SM, detectable H(2)O(2)-induced strand breaks decreased as SM concentration increased up to 30 muM; at 30 muM and above, the response with H(2)O(2) plus SM was similar to that with SM alone. Interference with the detection of H(2)O(2)-induced DNA strand breaks appears to be SM concentration-dependent up to 30 muM, and independent of SM concentration at >/=30 muM. This is presumably due to SM-induced cross-linking. It follows that cross-linking in DNA of SM-exposed PBL also interferes with DNA migration and detection of DNA strand breaks when cells are exposed to SM alone.

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What this paper is about

Sulfur mustard (SM) is a blistering agent that produces DNA strand breaks. To detect SM-induced DNA single strand breaks in human peripheral blood lymphocytes (PBL), cells were exposed to various concentrations of SM (10 to 1000 muM), and the comet assay (single-cell gel electrophoresis) was performed. We observed a SM concentration- and time-dependent increase in detectable DNA damage. To test whether SM-induced DNA cross-linking inhibits DNA migration in the comet assay, PBL were exposed to a) SM alone (10 to 1000 muM), b) H(2)O(2) (0.001%), which produces DNA single strand breaks with no cross-links, or c) SM followed at 2, 4, or 6 h by H(2)O(2). With H(2)O(2) alone, a large amount of strand breakage was detected. With H(2)O(2) plus SM, detectable H(2)O(2)-induced strand breaks decreased as SM concentration increased up to 30 muM; at 30 muM and above, the response with H(2)O(2) plus SM was similar to that with SM alone. Interference with the detection of H(2)O(2)-induced DNA strand breaks appears to be SM concentration-dependent up to 30 muM, and independent of SM concentration at >/=30 muM. This is presumably due to SM-induced cross-linking. It follows that cross-linking in DNA of SM-exposed PBL also interferes with DNA migration and detection of DNA strand breaks when cells are exposed to SM alone.

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Available abstract

Sulfur mustard (SM) is a blistering agent that produces DNA strand breaks. To detect SM-induced DNA single strand breaks in human peripheral blood lymphocytes (PBL), cells were exposed to various concentrations of SM (10 to 1000 muM), and the comet assay (single-cell gel electrophoresis) was performed. We observed a SM concentration- and time-dependent increase in detectable DNA damage. To test whether SM-induced DNA cross-linking inhibits DNA migration in the comet assay, PBL were exposed to a) SM alone (10 to 1000 muM), b) H(2)O(2) (0.001%), which produces DNA single strand breaks with no cross-links, or c) SM followed at 2, 4, or 6 h by H(2)O(2). With H(2)O(2) alone, a large amount of strand breakage was detected. With H(2)O(2) plus SM, detectable H(2)O(2)-induced strand breaks decreased as SM concentration increased up to 30 muM; at 30 muM and above, the response with H(2)O(2) plus SM was similar to that with SM alone. Interference with the detection of H(2)O(2)-induced DNA strand breaks appears to be SM concentration-dependent up to 30 muM, and independent of SM concentration at >/=30 muM. This is presumably due to SM-induced cross-linking. It follows that cross-linking in DNA of SM-exposed PBL also interferes with DNA migration and detection of DNA strand breaks when cells are exposed to SM alone.

Key concepts: Comet assay, DNA damage, DNA, Molecular biology, Gel electrophoresis, Chemistry, Peripheral blood, Biology

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