Altered expression of connexin43 in the inhibition of gap junctional intercellular communication by chlorohydroxyfuranones in WB-F344 rat liver epithelial cells

被引:13
作者
Hakulinen, P [1 ]
Rintala, E [1 ]
Mäki-Paakkanen, J [1 ]
Komulainen, H [1 ]
机构
[1] Natl Publ Hlth Inst, Toxicol Lab, FI-70701 Kuopio, Finland
关键词
chlorohydroxyfuranones; gap junctional intercellular communication; WB-F344; cells; connexin43; MX; 3-chloro-4-(dichloromethyl)-5-hydroxy-2(5H)-furanone;
D O I
10.1016/j.taap.2005.07.013
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
3-Chloro-4-(dichloromethyl)-5-hydroxy-2(5H)-furanone (MX), 3,4-dichloro-5-hydroxy-2(5H)-furanone (MCA), and 3-chloro-4-methyl-5-hydroxy-2(5H)-furanone (MCF) promote foci formation in the two-stage cell transformation assay in vitro. These chlorohydroxyfuranones (CHFs) and their structural congener 3-chloro-4-(chloromethyl)-5-hydroxy-2(5H)-furanone (CMCF) inhibit gap junctional intercellular communication (GJIC) in Balb/c 3T3 mouse fibroblast cells. In the present study, the effects of MX, MCA, CMCF, and MCF on GJIC were evaluated in liver cells (WB-F344 rat liver epithelial cells), the target cells of MX-induced carcinogenicity, using the scrape-loading dye transfer technique. The CHFs inhibited GJIC after I h exposure in a concentration-dependent fashion. The order of potency was MX > CMCF approximate to MCA > MCF. In terms of the lowest observed effective concentrations, the difference in the potency was about 27-fold (MX 1.875 mu M, MCF 50 mu M). After a prolonged exposure period (12 h), the inhibition of GJIC by MX and CMCF remained stable, but MCA and MCF exhibited increasing inhibitory effects. After removal of the CHFs, the GJIC slowly recovered. At the transcriptional level, CHFs caused essentially no change in the level of connexin43 (Cx43) mRNA. Preincubation of cells with the protein kinase C (PKC) inhibitor did not modify the response, but the specific MEK 1 inhibitor PD98059 decreased substantially the inhibition of GJIC by all four CHFs. Activation of the mitogen-activated protein kinases (MAPKs) signaling pathway was necessary for inhibition of GJIC. CHFs did not increase the basal phosphorylation state of the Cx43 protein, but all CHFs caused a concentration-dependent degradation of the Cx43 protein The results indicate that all the studied CHFs inhibit GJIC in WB-F344 cells by altering Cx43 expression. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:146 / 155
页数:10
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