Hepatic Inflammation and Fibrosis: Functional Links and Key Pathways

被引:1035
作者
Seki, Ekihiro [1 ,2 ]
Schwabe, Robert F. [3 ,4 ]
机构
[1] Univ Calif San Diego, Sch Med, Dept Med, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Sch Med, Dept Surg, La Jolla, CA 92093 USA
[3] Columbia Univ Coll Phys & Surg, Dept Med, New York, NY 10032 USA
[4] Columbia Univ Coll Phys & Surg, Inst Human Nutr, New York, NY 10032 USA
基金
美国国家卫生研究院;
关键词
NF-KAPPA-B; STELLATE CELL ACTIVATION; SINUSOIDAL ENDOTHELIAL-CELLS; CHRONIC VIRAL-HEPATITIS; CHRONIC LIVER-INJURY; GROWTH-FACTOR-BETA; NONALCOHOLIC STEATOHEPATITIS; NATURAL-KILLER; INTERFERON-GAMMA; T-CELLS;
D O I
10.1002/hep.27332
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
Inflammation is one of the most characteristic features of chronic liver disease of viral, alcoholic, fatty, and autoimmune origin. Inflammation is typically present in all disease stages and associated with the development of fibrosis, cirrhosis, and hepatocellular carcinoma. In the past decade, numerous studies have contributed to improved understanding of the links between hepatic inflammation and fibrosis. Here, we review mechanisms that link inflammation with the development of liver fibrosis, focusing on the role of inflammatory mediators in hepatic stellate cell (HSC) activation and HSC survival during fibrogenesis and fibrosis regression. We will summarize the contributions of different inflammatory cells, including hepatic macrophages, T and B lymphocytes, natural killer cells and platelets, as well as key effectors, such as cytokines, chemokines, and damage-associated molecular patterns. Furthermore, we will discuss the relevance of inflammatory signaling pathways for clinical liver disease and for the development of antifibrogenic strategies. (Hepatology 2015;61:1066-1079)
引用
收藏
页码:1066 / 1079
页数:14
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