Mechanisms of hepatic fibrogenesis

被引:1227
作者
Lee, Ursula E. [1 ]
Friedman, Scott L. [1 ]
机构
[1] Mt Sinai Sch Med, Div Liver Dis, New York, NY 10029 USA
关键词
Stellate cell; Fibrogenesis; Tyrosine kinase; Growth factors; Immune cells; Adipokines; TISSUE GROWTH-FACTOR; CHRONIC LIVER-INJURY; FAT-STORING CELLS; FIBROSIS IN-VIVO; STELLATE CELLS; RAT-LIVER; NONALCOHOLIC STEATOHEPATITIS; IMMUNE-RESPONSE; NADPH OXIDASE; RECEPTOR;
D O I
10.1016/j.bpg.2011.02.005
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
Multiple etiologies of liver disease lead to liver fibrosis through integrated signaling networks that regulate the deposition of extracellular matrix. This cascade of responses drives the activation of hepatic stellate cells (HSCs) into a myofibroblast-like phenotype that is contractile, proliferative and fibrogenic. Collagen and other extracellular matrix (ECM) components are deposited as the liver generates a wound-healing response to encapsulate injury. Sustained fibrogenesis leads to cirrhosis, characterized by a distortion of the liver parenchyma and vascular architecture. Uncovering the intricate mechanisms that underlie liver fibrogenesis forms the basis for efforts to develop targeted therapies to reverse the fibrotic response and improve the outcomes of patients with chronic liver disease. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:195 / 206
页数:12
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