Animal Models for Fibrotic Liver Diseases: What We Have, What We Need, and What Is under Development

被引:123
作者
Delire, Benedicte [1 ]
Starkel, Peter [1 ,2 ,3 ]
Leclercq, Isabelle [1 ]
机构
[1] Catholic Univ Louvain UCL, IREC, Lab Hepatogastroenterol, Ave E Mounier 53,Box B1-52-01, B-1200 Brussels, Belgium
[2] Catholic Univ Louvain, St Luc Acad Hosp, Dept Gastroenterol, Brussels, Belgium
[3] Catholic Univ Louvain, Inst Clin Res, Brussels, Belgium
关键词
Liver; Fibrosis; Hepatic stellate cell; Animal models; Cell tracking;
D O I
10.14218/JCTH.2014.00035
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Liver fibrosis is part of the wound-healing response to liver damage of various origins and represents a major health problem. Although our understanding of the pathogenesis of liver fibrosis has grown considerably over the last 20 years, effective antifibrotic therapies are still lacking. The use of animal models is crucial for determining mechanisms underlying initiation, progression, and resolution of fibrosis and for developing novel therapies. To date, no animal model can recapitulate all the hepatic and extra-hepatic features of liver disease. In this review, we will discuss the current rodent models of liver injuries. We will then focus on the available ways to target specifically particular compounds of fibrogenesis and on the new models of liver diseases like the humanized liver mouse model. (C) 2015 The Second Affiliated Hospital of Chongqing Medical University. Published by XIA & HE Publishing Ltd. All rights reserved.
引用
收藏
页码:53 / 66
页数:14
相关论文
共 126 条
[61]   Animal models of NASH: Getting both pathology and metabolic context right [J].
Larter, Claire Z. ;
Yeh, Matthew M. .
JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2008, 23 (11) :1635-1648
[62]   Intrahepatic insulin resistance in a murine model of steatohepatitis:: effect of PPARγ agonist pioglitazone [J].
Leclercq, Isabelle A. ;
Lebrun, Valerie A. ;
Starkel, Peter ;
Horsmans, Yves J. .
LABORATORY INVESTIGATION, 2007, 87 (01) :56-65
[63]   Mechanisms of hepatic fibrogenesis [J].
Lee, Ursula E. ;
Friedman, Scott L. .
BEST PRACTICE & RESEARCH CLINICAL GASTROENTEROLOGY, 2011, 25 (02) :195-206
[64]  
LEO MA, 1983, HEPATOLOGY, V3, P1
[65]  
Leung Patrick S C, 2012, Methods Mol Biol, V900, P291, DOI 10.1007/978-1-60761-720-4_14
[66]   Reproducible production of thioacetamide-induced macronodular cirrhosis in the rat with no mortality [J].
Li, XN ;
Benjamin, IS ;
Alexander, B .
JOURNAL OF HEPATOLOGY, 2002, 36 (04) :488-493
[67]   Experimental liver fibrosis research: update on animal models, legal issues and translational aspects [J].
Liedtke, Christian ;
Luedde, Tom ;
Sauerbruch, Tilman ;
Scholten, David ;
Streetz, Konrad ;
Tacke, Frank ;
Tolba, Rene ;
Trautwein, Christian ;
Trebicka, Jonel ;
Weiskirchen, Ralf .
FIBROGENESIS & TISSUE REPAIR, 2013, 6
[68]   Hepatitis C virus infection and related liver disease: the quest for the best animal model [J].
Mailly, Laurent ;
Robinet, Eric ;
Meuleman, Philip ;
Baumert, Thomas F. ;
Zeisel, Mirjam B. .
FRONTIERS IN MICROBIOLOGY, 2013, 4
[69]   Postulated carbon tetrachloride mode of action: A review [J].
Manibusan, Mary K. ;
Odin, Marc ;
Eastmond, David A. .
JOURNAL OF ENVIRONMENTAL SCIENCE AND HEALTH PART C-ENVIRONMENTAL CARCINOGENESIS & ECOTOXICOLOGY REVIEWS, 2007, 25 (03) :185-209
[70]   Gene Expression Profiling of Early Hepatic Stellate Cell Activation Reveals a Role for Igfbp3 in Cell Migration [J].
Mannaerts, Inge ;
Schroyen, Ben ;
Verhulst, Stefaan ;
Van Lommel, Leentje ;
Schuit, Frans ;
Nyssen, Marc ;
van Grunsven, Leo A. .
PLOS ONE, 2013, 8 (12)