DNA STRAND BREAKAGE, CYTOTOXICITY AND MUTAGENICITY OF HYDROGEN-PEROXIDE TREATMENT AT 4-DEGREES-C AND 37-DEGREES-C IN L5178Y SUBLINES

被引:60
作者
KRUSZEWSKI, M [1 ]
GREEN, MHL [1 ]
LOWE, JE [1 ]
SZUMIEL, I [1 ]
机构
[1] UNIV SUSSEX, MRC, CELL MUTAT UNIT, BRIGHTON BN1 9RR, ENGLAND
来源
MUTATION RESEARCH | 1994年 / 308卷 / 02期
关键词
HYDROGEN PEROXIDE; SINGLE-CELL GEL ELECTROPHORESIS; L5178Y MURINE LYMPHOMA SUBLINES;
D O I
10.1016/0027-5107(94)90158-9
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Cells from the L5178Y murine lymphoma subline LY-R are twofold more resistant to killing by ionizing radiation than the subline LY-S. In contrast, LY-R cells are more sensitive to killing by hydrogen peroxide. Cells of the two sublines in logarithmic growth phase were treated with hydrogen peroxide in phosphate-buffered saline for 1 h at 4 degrees C or 37 degrees C. From the comparison of D-o values it followed that at 37 degrees C LY-R were 3.6 times more sensitive to the killing effect of H2O2 than LY-S cells; at 4 degrees C they were 11 times more sensitive. Treatment with hydrogen peroxide at 4 degrees C gave a considerable sparing effect, which was substantially greater for the LY-S subline; for LY-S cells D, was 5.7 times lower at 37 degrees C than at 4 degrees C, for LY-R cells only 1.9 times. The mutation frequency (HGPRT) in LY-R cells was increased in proportion to H2O2 concentration and was the same at both treatment temperatures. In contrast, mutation frequencies initially increased, then decreased with increasing H2O2 concentration in LY-S cells treated at 4 or 37 degrees C. The concentration at which the decline was initiated was higher at 4 than at 37 degrees C. DNA damage after H2O2 treatment (both temperatures, 5 min) was estimated from the 'comet' assay (single-cell gel electrophoresis). The initial damage, but not the residual damage, differed significantly in LY sublines. A period of slower repair (between 3 and 10 min) was found in LY-R cells.
引用
收藏
页码:233 / 241
页数:9
相关论文
共 32 条
[1]   ELABORATION OF CELLULAR DNA BREAKS BY HYDROPEROXIDES [J].
BAKER, MA ;
HE, SQ .
FREE RADICAL BIOLOGY AND MEDICINE, 1991, 11 (06) :563-572
[2]  
BEER JZ, 1984, BRIT J CANCER, V49, P107
[3]   HYDROGEN PEROXIDE-INDUCED BASE DAMAGE IN DEOXYRIBONUCLEIC-ACID [J].
BLAKELY, WF ;
FUCIARELLI, AF ;
WEGHER, BJ ;
DIZDAROGLU, M .
RADIATION RESEARCH, 1990, 121 (03) :338-343
[4]   HYDROGEN-PEROXIDE INDUCED REPRODUCTIVE AND INTERPHASE DEATH IN 2 STRAINS OF L5178Y MURINE LYMPHOMA DIFFERING IN RADIATION SENSITIVITY [J].
BOUZYK, E ;
BURACZEWSKA, I ;
ROSIEK, O ;
SOCHANOWICZ, B ;
SZUMIEL, I .
RADIATION AND ENVIRONMENTAL BIOPHYSICS, 1991, 30 (02) :105-116
[5]   VALIDATION AND CHARACTERIZATION OF THE L5178Y-TK+/- MOUSE LYMPHOMA MUTAGEN ASSAY SYSTEM [J].
CLIVE, D ;
JOHNSON, KO ;
SPECTOR, JFS ;
BATSON, AG ;
BROWN, MMM .
MUTATION RESEARCH, 1979, 59 (01) :61-108
[6]   CORRELATION BETWEEN THERMAL RADIOSENSITIZATION AND HEAT-INDUCED LOSS OF DNA POLYMERASE-BETA ACTIVITY IN CHO CELLS [J].
DIKOMEY, E ;
JUNG, H .
INTERNATIONAL JOURNAL OF RADIATION BIOLOGY, 1993, 63 (02) :215-221
[7]   LOCUS SPECIFICITY IN THE MUTABILITY OF L5178Y MOUSE LYMPHOMA-CELLS - THE ROLE OF MULTILOCUS LESIONS [J].
EVANS, HH ;
MENCL, J ;
HORNG, MF ;
RICANATI, M ;
SANCHEZ, C ;
HOZIER, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (12) :4379-4383
[8]   UV-C SENSITIVITY OF UNSTIMULATED AND STIMULATED HUMAN-LYMPHOCYTES FROM NORMAL AND XERODERMA-PIGMENTOSUM DONORS IN THE COMET ASSAY - A POTENTIAL DIAGNOSTIC-TECHNIQUE [J].
GREEN, MHL ;
LOWE, JE ;
HARCOURT, SA ;
AKINLUYI, P ;
ROWE, T ;
COLE, J ;
ANSTEY, AV ;
ARLETT, CF .
MUTATION RESEARCH, 1992, 273 (02) :137-144
[9]   REVERSIBLE AND IRREVERSIBLE OXIDANT INJURY TO PC12 CELLS BY HYDROGEN-PEROXIDE [J].
HALLECK, MM ;
RICHBURG, JH ;
KAUFFMAN, FC .
FREE RADICAL BIOLOGY AND MEDICINE, 1992, 12 (02) :137-144
[10]   INDUCTION BY H2O2 OF DNA AND INTERPHASE CHROMOSOME-DAMAGE IN PLATEAU-PHASE CHINESE-HAMSTER OVARY CELLS [J].
ILIAKIS, GE ;
PANTELIAS, GE ;
OKAYASU, R ;
BLAKELY, WF .
RADIATION RESEARCH, 1992, 131 (02) :192-203