Effects of bile acids on biliary epithelial cells:: Proliferation, cytotoxicity, and cytokine secretion

被引:76
作者
Lamireau, T
Zoltowska, M
Levy, E
Yousef, I
Rosenbaum, J
Tuchweber, B
Desmoulière, A
机构
[1] Univ Bordeaux 2, Grp Rech Etud Foie, INSERM, E9917, F-33076 Bordeaux, France
[2] Hop St Justine, Unite Rech Gastroenterol Nutr, Ctr Rech, Montreal, PQ H3T 1C5, Canada
[3] Univ Montreal, Dept Nutr, Montreal, PQ H3C 3J7, Canada
[4] Univ Montreal, Dept Pharmacol, Montreal, PQ H3C 3J7, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
cholestasis; apoptosis; monocyte chemotactic protein-1; interleukin-6;
D O I
10.1016/S0024-3205(02)02408-6
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Hydrophobic bile acids, which are known to be cytotoxic for hepatocytes, are retained in high amount in the liver during cholestasis. Thus, we have investigated the effects, of bile acids with various hydrophobicities on biliary epithelial cells. Biliary epithelial cells were cultured in the presence of tauroursodeoxycholate (TUDC), taurocholate (TC), taurodeoxycholate (TDC), taurochenodeoxycholate (TCDC), or taurolithocholate (TLC). Cell proliferation, viability, apoptosis and secretion of monocyte chemotactic protein-1 (MCP-1) and of interleukin-6 (IL-6) were studied. Cell proliferation was increased by TDC, and markedly decreased by TLC in a dose dependant manner (50-500 muM). Cell viability was significantly decreased by TLC and TCDC at 500 muM. TLC, TDC and TCDC induced apoptosis at high concentrations. The secretion of MCP-1 and IL-6 was markedly stimulated by TC. TUDC had no significant effect on any parameter. These findings demonstrate that hydrophobic bile acids were cytotoxic and induced apoptosis of biliary epithelial cells. Furthermore, TC, a major biliary acid in human bile, stimulated secretion of cytokines involved in the inflammatory and fibrotic processes occurring during cholestatic liver diseases. (C) 2002 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:1401 / 1411
页数:11
相关论文
共 43 条
[21]  
KAKUMU S, 1991, AM J GASTROENTEROL, V86, P1804
[22]   Functional heterogeneity of the intrahepatic biliary epithelium [J].
Kanno, N ;
LeSage, G ;
Glaser, S ;
Alvaro, D ;
Alpini, G .
HEPATOLOGY, 2000, 31 (03) :555-561
[23]   Increased toxin-induced liver injury and fibrosis in interleukin-6-deficient mice [J].
Kovalovich, K ;
DeAngelis, RA ;
Li, W ;
Furth, EE ;
Ciliberto, G ;
Taub, R .
HEPATOLOGY, 2000, 31 (01) :149-159
[24]  
LOWRY OH, 1951, J BIOL CHEM, V193, P265
[25]   Monocyte chemotactic protein-1 as a chemoattractant for human hepatic stellate cells [J].
Marra, F ;
Romanelli, RG ;
Giannini, C ;
Failli, P ;
Pastacaldi, S ;
Arrighi, MC ;
Pinzani, M ;
Laffi, G ;
Montalto, P ;
Gentilini, P .
HEPATOLOGY, 1999, 29 (01) :140-148
[26]  
Marra F, 1998, AM J PATHOL, V152, P423
[27]  
MAUAD TH, 1994, AM J PATHOL, V145, P1237
[28]   INCREASED INTRAHEPATIC MESSENGER-RNA EXPRESSION OF INTERLEUKIN-2, INTERLEUKIN-6, AND INTERLEUKIN-8 IN HUMAN CIRRHOSIS [J].
NAPOLI, J ;
BISHOP, GA ;
MCCAUGHAN, GW .
GASTROENTEROLOGY, 1994, 107 (03) :789-798
[29]   Attenuated liver fibrosis and depressed serum albumin levels in carbon tetrachloride-treated IL-6-deficient mice [J].
Natsume, M ;
Tsuji, H ;
Harada, A ;
Akiyama, M ;
Yano, T ;
Ishikura, H ;
Nakanishi, I ;
Matsushima, K ;
Kaneko, S ;
Mukaida, N .
JOURNAL OF LEUKOCYTE BIOLOGY, 1999, 66 (04) :601-608
[30]   CHARACTERIZATION AND RESPONSE TO INTERLEUKIN-1 AND TUMOR-NECROSIS-FACTOR OF IMMORTALIZED MURINE BILIARY EPITHELIAL-CELLS [J].
PARADIS, K ;
LE, ONL ;
RUSSO, P ;
STCYR, M ;
FOURNIER, H ;
BU, DW .
GASTROENTEROLOGY, 1995, 109 (04) :1308-1315