Pathogenesis of Cholestatic Liver Disease and Therapeutic Approaches

被引:281
作者
Hirschfield, Gideon M. [2 ,3 ]
Heathcote, E. Jenny [2 ,3 ]
Gershwin, M. Eric [1 ]
机构
[1] Univ Calif Davis, Sch Med, Div Rheumatol Allergy & Clin Immunol, Davis, CA 95616 USA
[2] Toronto Western Hosp, Ctr Liver, Toronto, ON M5T 2S8, Canada
[3] Univ Toronto, Dept Med, Toronto, ON, Canada
基金
美国国家卫生研究院;
关键词
Primary Biliary Cirrhosis; Primary Sclerosing Cholangitis; Cholestasis; Ursodeoxycholic Acid; PRIMARY BILIARY-CIRRHOSIS; PRIMARY SCLEROSING CHOLANGITIS; REGULATORY T-CELLS; PYRUVATE-DEHYDROGENASE COMPLEX; INFLAMMATORY-BOWEL-DISEASE; INTRAHEPATIC BILE-DUCTS; ACID RECEPTOR TGR5; URSODEOXYCHOLIC ACID; ANTIMITOCHONDRIAL ANTIBODIES; EPITHELIAL-CELLS;
D O I
10.1053/j.gastro.2010.09.004
中图分类号
R57 [消化系及腹部疾病];
学科分类号
100201 [内科学];
摘要
Cholestatic liver disorders are caused by genetic defects, mechanical aberrations, toxins, or dysregulations in the immune system that damage the bile ducts and cause accumulation of bile and liver tissue damage. They have common clinical manifestations and pathogenic features that include the responses of cholangiocytes and hepatocytes to injury. We review the features of bile acid transport, tissue repair and regulation, apoptosis, vascular supply, immune regulation, and cholangiocytes that are associated with cholestatic liver disorders. We now have a greater understanding of the physiology of cholangiocytes at the cellular and molecular levels, as well as genetic factors, repair pathways, and autoimmunity mechanisms involved in the pathogenesis of disease. These discoveries will hopefully lead to new therapeutic approaches for patients with cholestatic liver disease.
引用
收藏
页码:1481 / 1496
页数:16
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