CADMIUM ACCUMULATION AND CYTOTOXICITY IN RAT HEPATOCYTES COCULTURED WITH A LIVER EPITHELIAL-CELL LINE

被引:13
作者
CARRERA, G
MELGAR, J
ALARY, J
LAMBOEUF, Y
MARTEL, P
机构
[1] INRA,F-78350 JOUY EN JOSAS,FRANCE
[2] UNIV SANTIAGO DE COMPOSTELA,E-27002 LUGO,SPAIN
关键词
D O I
10.1016/0887-2333(92)90033-N
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Cadmium accumulation and cytotoxicity were compared in hepatocytes in primary culture (HPC) or co-cultured (COC) with a rat liver epithelial cell line (RLEC). Cells were exposed for a 15-day period at 0, 0.045, 0.45 and 0.9-mu-m-Cd in the incubation medium. Cadmium uptake in COC was always linearly Cd dose and time dependent. In contrast, at the two highest doses for RLEC and only at the highest dose for HPC, a plateau in Cd uptake was observed. In viable cells 95% of the intracellular Cd was found in the cytosol, entirely protein bound. In the three types of culture the amount of Cd-metallothionein (MT) complex was proportional to Cd uptake and was in the order: COC > HPC > RLEC. Lactate dehydrogenase release in the medium and the DNA content of the plated cells at the end of exposure accounted for a marked Cd-induced cytotoxic effect in RLEC and a lesser effect in HPC. In contrast, no significant cytolysis was observed in COC. This suggests that although greater Cd accumulation was observed in COC than in HpC and RLEC, the detoxification procedure, dependent on Cd-MT complex formation, was more efficient and longer preserved in COC owing to a greater maintenance of hepatocyte specific functions, as evidenced by albumin secretion. This COC model offers a powerful tool for studying long-term accumulation and cytotoxicity of Cd in vitro at low exposure levels.
引用
收藏
页码:201 / 206
页数:6
相关论文
共 40 条
[1]   THE MODULATION BY METALLOTHIONEIN OF CADMIUM-INDUCED CYTOTOXICITY IN PRIMARY HEPATOCYTE CULTURES [J].
BEATTIE, JH ;
MARION, M ;
DENIZEAU, F .
TOXICOLOGY, 1987, 44 (03) :329-339
[2]   PROLONGED MAINTENANCE OF ACTIVE CYTOCHROME-P-450 IN ADULT-RAT HEPATOCYTES CO-CULTURED WITH ANOTHER LIVER-CELL TYPE [J].
BEGUE, JM ;
GUGUENGUILLOUZO, C ;
PASDELOUP, N ;
GUILLOUZO, A .
HEPATOLOGY, 1984, 4 (05) :839-842
[4]   METABOLISM OF CHLORPROPHAM BY ADULT-RAT HEPATOCYTES COCULTURED WITH A LIVER EPITHELIAL-CELL LINE [J].
CARRERA, G ;
ALARY, J ;
LAMBOEUF, Y ;
ANGLADE, F ;
ESCRIEUT, C ;
PINCHON, C .
FOOD ADDITIVES AND CONTAMINANTS, 1990, 7 :S152-S154
[5]   PROPERTIES OF CADMIUM-BINDING PROTEINS IN RAT TESTES - CHARACTERISTICS UNLIKE METALLOTHIONEIN [J].
DEAGEN, JT ;
WHANGER, PD .
BIOCHEMICAL JOURNAL, 1985, 231 (02) :279-283
[6]   CADMIUM-INDUCED HEPATIC AND RENAL INJURY IN CHRONICALLY EXPOSED RATS - LIKELY ROLE OF HEPATIC CADMIUM-METALLOTHIONEIN IN NEPHROTOXICITY [J].
DUDLEY, RE ;
GAMMAL, LM ;
KLAASSEN, CD .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1985, 77 (03) :414-426
[7]   EVALUATION OF THE CD HEMOGLOBIN AFFINITY ASSAY FOR THE RAPID-DETERMINATION OF METALLOTHIONEIN IN BIOLOGICAL TISSUES [J].
EATON, DL ;
TOAL, BF .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1982, 66 (01) :134-142
[8]   DEPENDENCE OF HEPATOCYTE-SPECIFIC GENE-EXPRESSION ON CELL-CELL INTERACTIONS IN PRIMARY CULTURE [J].
FRASLIN, JM ;
KNEIP, B ;
VAULONT, S ;
GLAISE, D ;
MUNNICH, A ;
GUGUENGUILLOUZO, C .
EMBO JOURNAL, 1985, 4 (10) :2487-2491
[9]  
FRAZIER JM, 1978, TOXICOL APPL PHARM, V43, P461, DOI 10.1016/S0041-008X(78)80005-2
[10]   GLYCOSAMINOGLYCANS AND PROTEOGLYCANS INDUCE GAP JUNCTION EXPRESSION AND RESTORE TRANSCRIPTION OF TISSUE-SPECIFIC MESSENGER-RNAS IN PRIMARY LIVER CULTURES [J].
FUJITA, M ;
SPRAY, DC ;
CHOI, H ;
SAEZ, JC ;
WATANABE, T ;
ROSENBERG, LC ;
HERTZBERG, EL ;
REID, LM .
HEPATOLOGY, 1987, 7 (01) :S1-S9