CYTOTOXICITY OF OXIDANTS AND ASBESTOS FIBERS IN CULTURED HUMAN MESOTHELIAL CELLS

被引:46
作者
KINNULA, VL
AALTO, K
RAIVIO, KO
WALLES, S
LINNAINMAA, K
机构
[1] UNIV HELSINKI,DEPT PEDIAT,SF-00290 HELSINKI,FINLAND
[2] NATL INST OCCUPAT HLTH,S-17184 SOLNA,SWEDEN
[3] INST OCCUPAT HLTH,HELSINKI,FINLAND
基金
芬兰科学院;
关键词
MESOTHELIAL CELLS; ASBESTOS; AMOSITE; HYDROGEN PEROXIDE; SUPEROXIDE; OXIDANTS; ANTIOXIDANTS; DNA STRAND BREAKS; FREE RADICALS;
D O I
10.1016/0891-5849(94)90140-6
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The authors investigated the mechanisms caused by oxidants (superoxide and hydrogen peroxide) and asbestos (amosite) fibers in human mesothelial cells. Immortalized human pleural mesothelial cells (MET 5A) were exposed in vitro to one of the following: hypoxanthine (100-200 mu M) plus xanthine oxidase (10-20 mU/ml) as a superoxide-generating system, H2O2 (50 mu M-5 mM); or amosite (1-100 mu g/cm(2)). Cellular adenine nucleotide depletion, DNA single strand breaks, extracellular release of nucleotides, and their catabolites and lactate dehydrogenase (LDH) were assessed as markers of cell damage after 4-6 h exposure to the oxidants or fibers. The effect of intracellular antioxidant enzymes and exogenous antioxidants on cell damage were investigated during oxidant and amosite exposure. Superoxide radical and H2O2 exposure resulted in the depletion of adenine nucleotides, accumulation of the products of nucleotide catabolism, induction of DNA single strand breaks, and extracellular LDH release. Amosite exposure did not cause nucleotide depletion or induction of DNA single strand breaks. Inactivation of the intracellular antioxidant enzymes glutathione reductase or catalase augmented cell damage during H2O2 exposure but not during amosite exposure.
引用
收藏
页码:169 / 176
页数:8
相关论文
共 43 条
[1]   ADENINE-NUCLEOTIDE DEPLETION FROM ENDOTHELIAL-CELLS EXPOSED TO XANTHINE-OXIDASE [J].
AALTO, TK ;
RAIVIO, KO .
AMERICAN JOURNAL OF PHYSIOLOGY, 1990, 259 (06) :C883-C888
[2]  
ANDREOLI SP, 1986, J LAB CLIN MED, V108, P190
[3]   INACTIVATION OF GLUTATHIONE REDUCTASE BY 2-CHLOROETHYL NITROSOUREA-DERIVED ISOCYANATES [J].
BABSON, JR ;
REED, DJ .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1978, 83 (02) :754-762
[4]  
Bergmeyer HU, 1974, METHOD ENZYMAT AN, P574
[5]  
Beutler E., 1975, RED CELL METABOLISM, V2nd, P71
[6]  
BUCKLEY BJ, 1991, J BIOL CHEM, V266, P16659
[7]   MECHANISMS OF EXTRACELLULAR HYDROGEN-PEROXIDE CLEARANCE BY ALVEOLAR TYPE-II PNEUMOCYTES [J].
ENGSTROM, PC ;
EASTERLING, L ;
BAKER, RR ;
MATALON, S .
JOURNAL OF APPLIED PHYSIOLOGY, 1990, 69 (06) :2078-2084
[8]   SINGLE-STRAND BREAKS IN DNA DURING REPAIR OF UV-INDUCED DAMAGE IN NORMAL HUMAN AND XERODERMA PIGMENTOSUM CELLS AS DETERMINED BY ALKALINE DNA UNWINDING AND HYDROXYLAPATITE CHROMATOGRAPHY - EFFECTS OF HYDROXYUREA, 5-FLUORODEOXYURIDINE AND 1-BETA-D-ARABINOFURANOSYLCYTOSINE ON THE KINETICS OF REPAIR [J].
ERIXON, K ;
AHNSTROM, G .
MUTATION RESEARCH, 1979, 59 (02) :257-271
[9]   DNA-REPAIR IN HUMAN BRONCHIAL EPITHELIAL-CELLS [J].
FORNACE, AJ ;
LECHNER, JF ;
GRAFSTROM, RC ;
HARRIS, CC .
CARCINOGENESIS, 1982, 3 (12) :1373-1377
[10]   STUDIES ON THE ROLE OF OXYGEN RADICALS IN ASBESTOS-INDUCED CYTOPATHOLOGY OF CULTURED HUMAN-LUNG MESOTHELIAL CELL [J].
GABRIELSON, EW ;
ROSEN, GM ;
GRAFSTROM, RC ;
STRAUSS, KE ;
HARRIS, CC .
CARCINOGENESIS, 1986, 7 (07) :1161-1164