Inhibitory effect of pentachlorophenol on gap junctional intercellular communication in rat liver epithelial cells in vitro

被引:44
作者
Sai, K
Upham, BL
Kang, KS
Hasegawa, R
Inoue, T
Trosko, JE
机构
[1] Natl Inst Hlth Sci, Div Cellular & Mol Toxicol, Setagaya Ku, Tokyo 1588501, Japan
[2] Michigan State Univ, Dept Pediat Human Dev, E Lansing, MI 48824 USA
关键词
pentachlorophenol; tetrachlorohydroquinone; gap junctional intercellular communication; hepatocarcinogenesis;
D O I
10.1016/S0304-3835(98)00082-2
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
To understand the initiating/promoting actions of pentachlorophenol (PCP), a non-mutagenic hepatocarcinogen, and its metabolite, tetrachlorohydroquinone (TCHQ), we investigated the effects of each chemical on gap junctional intercellular communication (GJIC) in rat liver epithelial cells (WB cells) by the scrape-loading and dye transfer method. After treatment with PCP, the GJIC was initially inhibited at 4 h but was restored in 6-8 h, followed by a second phase of inhibition between 16 and 24 h. Both the first and second inhibitions were concentration-dependent and were restored by 2-4 h after removal of PCP. The phosphorylation state of connexin 43 (CX43) and its localization on the plasma membrane were unchanged up to 24 h after treatment; however, this was accompanied by a decrease in the CX43 protein level. No inhibitory effect was apparent on the GJIC of cells treated with TCHQ. These results suggest that PCP may play a critical role of promoting activity via nonmutagenic mechanisms. (C) 1998 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:9 / 17
页数:9
相关论文
共 47 条
[21]  
KRUTOVSKIKH VA, 1995, LAB INVEST, V72, P571
[22]   JUNCTIONAL INTER-CELLULAR COMMUNICATION AND THE CONTROL OF GROWTH [J].
LOEWENSTEIN, WR .
BIOCHIMICA ET BIOPHYSICA ACTA, 1979, 560 (01) :1-65
[23]   CHANGES IN GAP-JUNCTION PERMEABILITY, PHOSPHORYLATION, AND NUMBER MEDIATED BY PHORBOL ESTER AND NON-PHORBOL-ESTER TUMOR PROMOTERS IN RAT-LIVER EPITHELIAL-CELLS [J].
MATESIC, DF ;
RUPP, HL ;
BONNEY, WJ ;
RUCH, RJ ;
TROSKO, JE .
MOLECULAR CARCINOGENESIS, 1994, 10 (04) :226-236
[24]   DIFFERENTIAL PHOSPHORYLATION OF THE GAP JUNCTION PROTEIN CONNEXIN-43 IN JUNCTIONAL COMMUNICATION-COMPETENT AND COMMUNICATION-DEFICIENT CELL-LINES [J].
MUSIL, LS ;
CUNNINGHAM, BA ;
EDELMAN, GM ;
GOODENOUGH, DA .
JOURNAL OF CELL BIOLOGY, 1990, 111 (05) :2077-2088
[25]   ROLE OF ACTIVE OXYGEN SPECIES IN DNA-DAMAGE BY PENTACHLOROPHENOL METABOLITES [J].
NAITO, S ;
ONO, Y ;
SOMIYA, I ;
INOUE, S ;
ITO, K ;
YAMAMOTO, K ;
KAWANISHI, S .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 1994, 310 (01) :79-88
[26]  
*NAT TOX PROGR, 1989, TR349 NTP
[27]   THE ROLE OF PROTEIN KINASE-C IN CELL-SURFACE SIGNAL TRANSDUCTION AND TUMOR PROMOTION [J].
NISHIZUKA, Y .
NATURE, 1984, 308 (5961) :693-698
[28]   TRANSCRIPTIONAL ACTIVATION OF EARLY-RESPONSE GENES BY HYDROGEN-PEROXIDE IN A MOUSE OSTEOBLASTIC CELL-LINE [J].
NOSE, K ;
SHIBANUMA, M ;
KIKUCHI, K ;
KAGEYAMA, H ;
SAKIYAMA, S ;
KUROKI, T .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1991, 201 (01) :99-106
[29]  
Rabes H M, 1985, Adv Enzyme Regul, V23, P241, DOI 10.1016/0065-2571(85)90050-0
[30]   LOSS OF GAP-JUNCTIONS FROM DDT-TREATED RAT-LIVER EPITHELIAL-CELLS [J].
RUCH, RJ ;
BONNEY, WJ ;
SIGLER, K ;
GUAN, XJ ;
MATESIC, D ;
SCHAFER, LD ;
DUPONT, E ;
TROSKO, JE .
CARCINOGENESIS, 1994, 15 (02) :301-306