Expression and function of the bile acid receptor TGR5 in Kupffer cells

被引:363
作者
Keitel, Verena [1 ]
Donner, Markus [1 ]
Winandy, Stefanie [1 ]
Kubitz, Ralf [1 ]
Haeussinger, Dieter [1 ]
机构
[1] Univ Dusseldorf, Clin Gastroenterol Hepatol & Infectiol, D-40225 Dusseldorf, Germany
关键词
TGR5; bile acids; Kupffer cells; cytokines; hepatic stellate cells; cholangiocytes; G-protein coupled receptor; cAMP;
D O I
10.1016/j.bbrc.2008.04.171
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Kupffer cells are resident macrophages in the liver and play a central role in the hepatic response to injury. Bile acids can impair macrophage function leading to decreased cytokine release. TGR5 is a novel, membrane-bound bile acid receptor, and it has been suggested that the immunosuppressive effect of bile acids can be mediated by TGR5. However, the function of TGR5 in Kupffer cells has not been studied and a direct link between TGR5 and cytokine production in macrophages has not been established. The present study demonstrates that TGR5 is localized in the plasma membrane of isolated Kupffer cells and is responsive to bile acids. Furthermore, bile acids inhibited LPS-induced cytokine expression in Kupffer cells via TGR5-cAMP dependent pathways. TGR5-immunoreactivity in Kupffer cells was increased in rat livers following bile-duct ligation, suggesting that TGR5 may play a protective role in obstructive cholestasis preventing excessive cytokine production thereby reducing liver injury. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:78 / 84
页数:7
相关论文
共 37 条
[1]   Bile acids stimulate proliferative and secretory events in large but not small cholangiocytes [J].
Alpini, G ;
Glaser, S ;
Robertson, W ;
Phinizy, JL ;
Rodgers, RE ;
Caligiuri, A ;
LeSage, G .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 1997, 273 (02) :G518-G529
[2]   Bile acid depletion and repletion regulate cholangiocyte growth and secretion by a phosphatidylinositol 3-kinase-dependent pathway in rats [J].
Alpini, G ;
Glaser, S ;
Alvaro, D ;
Ueno, Y ;
Marzioni, M ;
Francis, H ;
Baiocchi, L ;
Stati, T ;
Barbaro, B ;
Phinizy, JL ;
Mauldin, J ;
LeSage, G .
GASTROENTEROLOGY, 2002, 123 (04) :1226-1237
[3]   HEPATIC-UPTAKE OF BILE-ACIDS IN MAN - FASTING AND POSTPRANDIAL CONCENTRATIONS OF INDIVIDUAL BILE-ACIDS IN PORTAL VENOUS AND SYSTEMIC BLOOD-SERUM [J].
ANGELIN, B ;
BJORKHEM, I ;
EINARSSON, K ;
EWERTH, S .
JOURNAL OF CLINICAL INVESTIGATION, 1982, 70 (04) :724-731
[4]   CYTOKINES TUMOR-NECROSIS-FACTOR AND INTERLEUKIN-6 IN EXPERIMENTAL BILIARY OBSTRUCTION IN MICE [J].
BEMELMANS, MHA ;
GOUMA, DJ ;
GREVE, JW ;
BUURMAN, WA .
HEPATOLOGY, 1992, 15 (06) :1132-1136
[5]   Expression of glutamine synthetase in macrophages [J].
Bode, JG ;
Peters-Regehr, T ;
Kubitz, R ;
Häussinger, D .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 2000, 48 (03) :415-421
[6]   PREVENTION OF POSTOPERATIVE RENAL-FAILURE IN PATIENTS WITH OBSTRUCTIVE-JAUNDICE - THE ROLE OF BILE-SALTS [J].
CAHILL, CJ .
BRITISH JOURNAL OF SURGERY, 1983, 70 (10) :590-595
[7]   DIFFERENTIAL-EFFECTS OF CHENODEOXYCHOLIC AND URSODEOXYCHOLIC ACIDS ON INTERLEUKIN-1, INTERLEUKIN-6 AND TUMOR-NECROSIS-FACTOR-ALPHA PRODUCTION BY MONOCYTES [J].
CALMUS, Y ;
GUECHOT, J ;
PODEVIN, P ;
BONNEFIS, MT ;
GIBOUDEAU, J ;
POUPON, R .
HEPATOLOGY, 1992, 16 (03) :719-723
[8]   Concentration of unsulfated lithocholic acid in portal and systemic venous plasma: Evidence that lithocholic acid does not down regulate the hepatic cholesterol 7 alpha-hydroxylase activity in gallstone patients [J].
Einarsson, K ;
Alvelius, G ;
Hillebrant, CG ;
Reihner, E ;
Bjorkhem, I .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 1996, 1317 (01) :19-26
[9]  
FUKUSHIMA K, 1995, J LIPID RES, V36, P315
[10]   Tauroursodeoxycholic acid enhances phagocytosis of the cultured rat Kupffer cell [J].
Funaoka, M ;
Komatsu, M ;
Toyoshima, I ;
Mikami, K ;
Ono, T ;
Hoshino, T ;
Kato, J ;
Kuramitsu, T ;
Ishii, T ;
Masamune, O .
JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 1999, 14 (07) :652-658