Inhibition of cell-cell communication by methylsulfonyl metabolites of polychlorinated biphenyl congeners in rat liver epithelial IAR 20 cells

被引:18
作者
Kato, Y
Kenne, K
Haraguchi, K
Masuda, Y
Kimura, R
Wärngård, L
机构
[1] Univ Shizuoka, Sch Pharmaceut Sci, Shizuoka 422, Japan
[2] Karolinska Inst, Inst Environm Med, S-17177 Stockholm, Sweden
[3] Daiichi Coll Pharmaceut Sci, Minami Ku, Fukuoka 815, Japan
关键词
polychlorinated biphenyl; methylsulfonyl metabolite; gap junction intercellular communication; IAR 20 rat liver epithelial cell;
D O I
10.1007/s002040050484
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
The effects of three polychlorinated biphenyl (PCB) congeners and their six methylsulfonyl (MeSO2)-metabolites on cell communication have been investigated in the scrape-loading/dye-transfer assay in IAR 20 rat liver epithelial cells. The results demonstrated that at non-cytotoxic concentrations 2,2',4',5-tetrachlorobiphenyl, 2,2',4',5,5'-pentachlorobiphenyl (2,2',4',5,5'-pentaCB), 2,2',4',5,5',6-hexachlorobiphenyl (2,2',4',5,5', 6-hexa-CB), and their 3- and 4-MeSO2 derivatives completely inhibited the cell communication within 1 h. 4-MeSO2-2,2',4'5,5'-pentaCB and 4-MeSO2-2,2',4',5, 5',6-hexaCB appeared to inhibit the cell communication at slightly lower concentration than their parental PCB congeners and 3-MeSO2 derivatives. The results show that 3- and 4-MeSO2 derivatives of the PCB congeners tested inhibit gap junction intercellular communication at about the same potency as their parental compounds. Since inhibition of cell communication is often observed after treatment with many tumor promoters, our findings suggest that the metabolites may also act as tumor promoters.
引用
收藏
页码:178 / 182
页数:5
相关论文
共 38 条
[1]  
BERGMAN A, 1992, AMBIO, V21, P570
[2]  
BERGMAN A, 1994, ENVIRON TOXICOL CHEM, V13, P121, DOI [10.1897/1552-8618(1994)13[121:PADMSI]2.0.CO
[3]  
2, 10.1002/etc.5620130117]
[4]   POLYCHLORINATED-BIPHENYLS, CLASSIFIED AS EITHER PHENOBARBITAL-TYPE OR 3-METHYLCHOLANTHRENE-TYPE INDUCERS OF CYTOCHROME-P-450, ARE BOTH HEPATIC TUMOR PROMOTERS IN DIETHYLNITROSAMINE-INITIATED RATS [J].
BUCHMANN, A ;
KUNZ, W ;
WOLF, CR ;
OESCH, F ;
ROBERTSON, LW .
CANCER LETTERS, 1986, 32 (03) :243-253
[5]   EFFECTS OF POLYCHLORINATED-BIPHENYLS IN RAT-LIVER - CORRELATION BETWEEN PRIMARY SUBCELLULAR EFFECTS AND PROMOTING ACTIVITY [J].
BUCHMANN, A ;
ZIEGLER, S ;
WOLF, A ;
ROBERTSON, LW ;
DURHAM, SK ;
SCHWARZ, M .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1991, 111 (03) :454-468
[6]  
CADOGAN JIG, 1962, J CHEM SOC, P4257
[7]   COPLANAR PCBS IN HUMAN-MILK IN THE PROVINCE OF QUEBEC, CANADA - ARE THEY MORE TOXIC THAN DIOXIN FOR BREAST FED INFANTS [J].
DEWAILLY, E ;
WEBER, JP ;
GINGRAS, S ;
LALIBERTE, C .
BULLETIN OF ENVIRONMENTAL CONTAMINATION AND TOXICOLOGY, 1991, 47 (04) :491-498
[8]  
DIWAN BA, 1988, CANCER RES, V48, P2492
[9]   SCRAPE-LOADING AND DYE TRANSFER - A RAPID AND SIMPLE TECHNIQUE TO STUDY GAP JUNCTIONAL INTERCELLULAR COMMUNICATION [J].
ELFOULY, MH ;
TROSKO, JE ;
CHANG, CC .
EXPERIMENTAL CELL RESEARCH, 1987, 168 (02) :422-430
[10]   SYNTHESIS AND CHARACTERIZATION OF TISSUE-RETAINABLE METHYLSULFONYL POLYCHLORINATED BIPHENYL ISOMERS [J].
HARAGUCHI, K ;
KUROKI, H ;
MASUDA, Y .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 1987, 35 (02) :178-182