DIFFERENTIAL CYTOTOXICITY OF CADMIUM TO RAT EMBRYONIC FIBROBLASTS AND HUMAN SKIN FIBROBLASTS

被引:23
作者
LIN, CJ [1 ]
WU, KH [1 ]
YEW, FH [1 ]
LEE, TC [1 ]
机构
[1] NATL TAIWAN UNIV, INST ZOOL, TAIPEI 10764, TAIWAN
关键词
D O I
10.1006/taap.1995.1122
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In order to identify why cadmium is differentially toxic to humans and rats, we compared cadmium-induced cytotoxic responses in rat embryonic fibroblasts (REF) and human skin fibroblasts (HFW), According to the values of the lethal concentration 50% for cadmium, REF were about 13-fold more sensitive than HFW to cadmium acetate (1.5 vs 25 mu M), Furthermore, progression of S phase cells was more severely delayed by cadmium in REF than in HFW, At doses that killed 90% of REF or HFW (5 or 50 mu M, respectively), 50% of DNA synthesis was inhibited in REF, whereas DNA synthesis was not apparently inhibited in HFW, The differential sensitivity to cadmium could not be simply due to different basal levels of metallothionein, since the cellular metallothionein content in HFW was only 1.6 times that in REF, and metallothionein was apparently induced by cadmium in both cells with similar synthesis rates. Furthermore, elevation of cellular metallothionein levels by zinc sulfate pretreatment decreased cadmium toxicity in both cell types, but did not alter their relative sensitivity to cadmium, The differential sensitivity was also not due to differences in cadmium accumulation, since HFW accumulated more cadmium than REF after a 24-hr exposure to 1 or 5 mu M cadmium acetate, Although most of the cadmium remained in the cytoplasm, the nuclei of REF contained 12-fold more cadmium than nuclei of HFW (1.31 vs 0.11 mu g Cd/mg nuclear protein). Therefore, our results indicate that a high level of cadmium accumulation in nuclei of REF may be responsible for cell killing through breakdown of nuclear functions, (C) 1995 Academic Press, Inc.
引用
收藏
页码:20 / 26
页数:7
相关论文
共 43 条
[31]   MAMMALIAN ZINC HOMEOSTASIS - REQUIREMENT FOR RNA AND METALLOTHIONEIN SYNTHESIS [J].
RICHARDS, MP ;
COUSINS, RJ .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1975, 64 (04) :1215-1223
[32]   CADMIUM RESISTANCE AND CONTENT OF CADMIUM-BINDING PROTEIN IN CULTURED HUMAN CELLS [J].
RUGSTAD, HE ;
NORSETH, T .
NATURE, 1975, 257 (5522) :136-137
[33]   UPTAKE AND SUBCELLULAR-DISTRIBUTION OF CADMIUM IN RESTING AND MITOGEN-ACTIVATED LYMPHOCYTES AND ITS RELATIONSHIP TO A METALLOTHIONEIN-LIKE PROTEIN [J].
SGAGIAS, M ;
BALTER, NJ ;
GRAY, I .
ENVIRONMENTAL RESEARCH, 1989, 49 (02) :262-270
[34]   INFIDELITY OF DNA-SYNTHESIS INVITRO - SCREENING FOR POTENTIAL METAL MUTAGENS OR CARCINOGENS [J].
SIROVER, MA ;
LOEB, LA .
SCIENCE, 1976, 194 (4272) :1434-1436
[35]  
SMITH JB, 1989, J BIOL CHEM, V264, P7115
[36]   CADMIUM SUBSTITUTION FOR ZINC IN FINGER-LOOP DOMAINS OF GENE-REGULATING PROTEINS AS A POSSIBLE MECHANISM FOR THE GENOTOXICITY AND CARCINOGENICITY OF CADMIUM COMPOUNDS [J].
SUNDERMAN, FW .
TOXICOLOGICAL AND ENVIRONMENTAL CHEMISTRY, 1990, 27 (1-3) :131-141
[37]   DEGENERATIVE PROCESSES IN SKELETAL-MUSCLE OF CD-2+-TREATED RATS AND CD-2+ INHIBITION OF MITOCHONDRIAL CA-2+ TRANSPORT [J].
TOURY, R ;
STELLY, N ;
BOISSONNEAU, E ;
DUPUIS, Y .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1985, 77 (01) :19-35
[38]  
WAALKES MP, 1989, BIOL TRACE ELEM RES, V21, P483
[39]  
WAALKES MP, 1989, CANCER RES, V49, P4282
[40]  
WAALKES MP, 1988, CANCER RES, V48, P4656