Induction of heme oxygenase in mammalian cells by mineral fibers: Distinctive effect of reactive oxygen species

被引:18
作者
Suzuki, K [1 ]
Hei, TK [1 ]
机构
[1] COLUMBIA UNIV COLL PHYS & SURG,CTR RADIOL RES,DEPT RADIAT ONCOL,NEW YORK,NY 10032
关键词
D O I
10.1093/carcin/17.4.661
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Exponentially growing human-hamster hybrid [A(L)] cells treated with a 40 mu g/ml (8 mu g/cm(2)) dose of UICC standard reference chrysotile fibers induced heme oxygenase (HO) protein with a maximum expression level at 8 h post-treatment, While the constitutive HO expression was detectable in non-treated A(L) cells, the protein level was increased similar to 4.5-fold in fiber-treated cells, The induction was dose-dependent at fiber concentration between 2.5 mu g/ml (0.5 mu g/cm(2)) and 40 mu g/ml (8 mu g/cm(2)) with the induced HO concentrated mostly in the cytoplasm as shown by immunostaining. Several other types of mineral fibers examined including crocidolites, tremolites, and erionites also induced HO synthesis with varying degree of efficiency. In general, chrysotile and crocidolite were more efficient inducers of HO than tremoiite and erionite when compared at fiber doses that resulted in similar to 50% survival (LD50) level. The effects of antioxidant enzymes on HO induction were examined by concurrent treatment of fiber-exposed cultures with SOD and catalase, Although addition of superoxide dismutase (SOD) and catalase inhibited HO induction in a dose-dependent manner, they offered no protection on fiber-mediated clonogenic toxicity in the same population of treated cells, These results suggest that reactive oxygen species (ROS) produced by asbestos fibers play an essential role in the induction of HO and that different mineral fibers, when applied at equitoxic doses, often result in different oxidative stress status as determined by the induction of HO proteins.
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页码:661 / 667
页数:7
相关论文
共 53 条
[1]  
APPLEGATE LA, 1991, CANCER RES, V51, P974
[2]  
Aust A., 1994, NATO ASI Series, VH85, P53
[3]  
BASUMODAK S, 1993, CANCER RES, V53, P4505
[4]   UV-A INDUCED LIPID-PEROXIDATION IN LIPOSOMAL MEMBRANE [J].
BOSE, B ;
AGARWAL, S ;
CHATTERJEE, SN .
RADIATION AND ENVIRONMENTAL BIOPHYSICS, 1989, 28 (01) :59-65
[5]   ROLE OF OXYGEN DERIVATIVES IN THE CYTOTOXICITY AND DNA-DAMAGE PRODUCED BY ASBESTOS ON RAT PLEURAL MESOTHELIAL CELLS IN-VIVO [J].
DONG, HY ;
BUARD, A ;
RENIER, A ;
LEVY, F ;
SAINTETIENNE, L ;
JAURAND, MC .
CARCINOGENESIS, 1994, 15 (06) :1251-1255
[6]   FORMATION OF A CLASTOGENIC FACTOR BY ASBESTOS-TREATED RAT PLEURAL MESOTHELIAL CELLS [J].
EMERIT, I ;
JAURAND, MC ;
SAINTETIENNE, L ;
LEVY, A .
AGENTS AND ACTIONS, 1991, 34 (3-4) :410-415
[7]   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
[8]   ASBESTOS-INDUCED ENDOTHELIAL-CELL ACTIVATION AND INJURY - DEMONSTRATION OF FIBER PHAGOCYTOSIS AND OXIDANT-DEPENDENT TOXICITY [J].
GARCIA, JGN ;
GRAY, LD ;
DODSON, RF ;
CALLAHAN, KS .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1988, 138 (04) :958-964
[9]  
GOODGLICK LA, 1990, CANCER RES, V50, P5153
[10]  
GOODGLICK LA, 1986, CANCER RES, V46, P5558