Role of TGR5 (GPBAR1) in Liver Disease

被引:74
作者
Keitel, Verena [1 ]
Haeussinger, Dieter [1 ]
机构
[1] Heinrich Heine Univ, Clin Gastroenterol Hepatol & Infect Dis, Univ Hosp Dusseldorf, Fac Med, Moorenstr 5, D-40225 Dusseldorf, Germany
关键词
bile acids; G protein-coupled receptor; steatohepatitis; cholangiopathy; inflammation; BILE-ACID RECEPTOR; GROWTH-FACTOR; 15; NUCLEAR RECEPTOR; TARGETED DISRUPTION; PROTEIN; IDENTIFICATION; ACTIVATION; INFLAMMATION; PHYSIOLOGY; FXR;
D O I
10.1055/s-0038-1669940
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
TGR5 (GPBAR1) is a G protein-coupled receptor activated by primary and secondary bile acids, which is expressed in different nonparenchymal cells of the liver, such as sinusoidal endothelial cells, Kupffer cells, cholangiocytes as well as activated hepatic stellate cells. In liver, TGR5 modulates microcirculation, inflammation, regeneration, biliary secretion and proliferation as well as gallbladder filling. Absence of TGR5 renders mice more susceptible toward infectious, inflammatory, metabolic as well as cholestatic liver injuries. It is unknown whether TGR5 plays a role in the pathogenesis of human nonalcoholic steatohepatitis and cholestatic liver diseases such as primary sclerosing cholangitis and primary biliary cholangitis. However, overexpression of TGR5 has been detected in human intra- and extrahepatic cholangiocarcinoma as well as in cystic cholangiocytes, where the receptor promotes cell proliferation, anti-apoptosis as well as cyst growth. While TGR5 agonists may improve various aspects of metabolic, inflammatory, and cholestatic liver diseases, TGR5 inhibitors may attenuate disease progression in polycystic liver disease and cholangiocarcinoma.
引用
收藏
页码:333 / 339
页数:7
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