Hepatic stellate cells and parasite-induced liver fibrosis

被引:80
|
作者
Anthony, Barrie [1 ]
Allen, Jeremy T. [2 ]
Li, Yuesheng S. [1 ]
McManus, Donald P. [1 ]
机构
[1] Queensland Inst Med Res, Brisbane, Qld 4029, Australia
[2] Univ Salford, Ctr Parasitol & Dis, Biomed Sci Res Inst, Manchester MS 4WT, Lancs, England
来源
PARASITES & VECTORS | 2010年 / 3卷
基金
英国医学研究理事会;
关键词
SCHISTOSOMA-MANSONI INFECTION; TRANSFORMING-GROWTH-FACTOR; SOLUBLE EGG ANTIGEN; TGF-BETA; ALVEOLAR ECHINOCOCCOSIS; PERIPORTAL FIBROSIS; COLLAGEN; JAPONICUM; GAMMA; EXPRESSION;
D O I
10.1186/1756-3305-3-60
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
Fibrogenesis is a common feature of many diseases where there is severe insult to the liver. The hepatic stellate cell trans-differentiation into a myofibroblast has been identified as an important event in liver fibrogenesis and has been well investigated over the last few years in a number of liver diseases. The trans-differentiation process can be monitored in vitro by evaluation of biomarkers that are characteristic of normal quiescent hepatic stellate cells or activated myofibroblasts. Two major parasitic diseases associated with liver injury and fibrosis are schistosomiasis and echinococcosis. Recent studies have highlighted a role for activated hepatic stellate cells in both murine and human schistosomiasis as well as demonstrating that schistosome antigens are able to regulate this trans-differentiation process. Study of the hepatic stellate cell and its interaction with parasite-derived antigens may be pivotal in our understanding of the pathology associated with schistosomiasis and other parasitic diseases, including echinococcosis, as well as revealing new information on the trans-differentiation process in this cell type.
引用
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页数:7
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