Pathogenesis of Liver Fibrosis

被引:1414
作者
Hernandez-Gea, Virginia [1 ]
Friedman, Scott L. [1 ]
机构
[1] Mt Sinai Sch Med, Div Liver Dis, New York, NY 10029 USA
来源
ANNUAL REVIEW OF PATHOLOGY: MECHANISMS OF DISEASE, VOL 6 | 2011年 / 6卷
关键词
hepatic stellate cells; extracellular matrix; cirrhosis; myofibroblasts; HEPATIC STELLATE-CELLS; TO-MESENCHYMAL TRANSITION; FAT-STORING CELLS; RENIN-ANGIOTENSIN SYSTEM; ACTIVATED RECEPTOR-GAMMA; HISTONE DEACETYLASE INHIBITOR; MYOCYTE ENHANCER FACTOR-2; ALPHA-1(I) COLLAGEN GENE; GROWTH-FACTOR RECEPTOR; BILE-DUCT LIGATION;
D O I
10.1146/annurev-pathol-011110-130246
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Liver fibrosis is a major cause of morbidity and mortality worldwide due to chronic viral hepatitis and, more recently, from fatty liver disease associated with obesity. Hepatic stellate cell activation represents a critical event in fibrosis because these cells become the primary source of extracellular matrix in liver upon injury. Use of cell-culture and animal models has expanded our understanding of the mechanisms underlying stellate cell activation and has shed new light on genetic regulation, the contribution of immune signaling, and the potential reversibility of the disease. As pathways of fibrogenesis are increasingly clarified, the key challenge will be translating new advances into the development of antifibrotic therapies for patients with chronic liver disease.
引用
收藏
页码:425 / 456
页数:32
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