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[Cancer Research 49, 4504-4508, August 15, 1989]
© 1989 American Association for Cancer Research

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Comparison of Sister Chromatid Exchanges in Spleen and Thymus Lymphocytes from AKR, C57BL/6N x DBA/2J F1, and CBA Mice following in Vivo Exposure to N-Methyl-N-nitrosourea

Robin E. Neft, Henry M. Schol and Daniel A. Casciano

Division of Genetic Toxicology, National Center for Toxicological Research, Food and Drug Administration, Department of Health and Human Services, Jefferson, Arkansas 72079 [R. E. N., H. M. S., D. A. C.]; and Department of Pharmacology and Toxicology and Department of Biochemistry, University of Arkansas for Medical Sciences, Little Rock, Arkansas 72205 [D. A. C.]

The induction of sister chromatid exchange (SCE) by N-methyl-N-nitrosourea (MNU) was studied in spleen and thymus lymphocytes from AKR mice, which are highly susceptible to MNU-produced thymomas, CBA mice, which are much less sensitive to induction of thymomas by MNU, and C57BL/6N x DBA/2J F1 mice. MNU produced dose-related increases in SCE in concanavalin A (Con A)- and lipopolysaccharidestimulated spleen lymphocytes and Con A-stimulated thymus lymphocytes from each mouse strain at 1 and 24 h posttreatment. MNU-induced SCE were generally higher in Con A-stimulated spleen lymphocytes compared to lipopolysaccharide-stimulated spleen lymphocytes and Con A-stimulated thymus lymphocytes from each mouse strain. On the whole, MNU-produced SCE were lower in AKR and CBA spleens than in C57BL/6N x DBA/2J F1 spleens. In addition, MNU-induced SCE levels in thymus lymphocytes from all three strains of mice were, for the most part, similar. These results indicate that if differences in MNU-induced genotoxicity in AKR, CBA, and C57BL/6N x DBA/2J F1 thymus lymphocytes exist, these differences cannot be ascertained by use of the in vivo/in vitro SCE assay.

Received 3/10/89. Revised 5/11/89. Accepted 5/18/89.







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
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Copyright © 1989 by the American Association for Cancer Research.