4.8 Article

A diet-induced animal model of non-alcoholic fatty liver disease and hepatocellular cancer

期刊

JOURNAL OF HEPATOLOGY
卷 65, 期 3, 页码 579-588

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.jhep.2016.05.005

关键词

Steatosis; Fibrosis; Hepatocyte ballooning; Hepatocellular carcinoma; Drug therapy

资金

  1. NIH [RO1 DK 081450, RO1 AA 020758, T32 DK 007150-38, R01 DK099558, U01HD087198, P30 CA016059]
  2. Irma T. Hirschl/Monique Weill-Caulier Trust
  3. Young Investigator Award from SCIEX for clinical lipidomic research

向作者/读者索取更多资源

Background & Aims: The lack of a preclinical model of progressive non-alcoholic steatohepatitis (NASH) that recapitulates human disease is a barrier to therapeutic development. Methods: A stable isogenic cross between C57BL/6J (B6) and 129S1/SvImJ (S129) mice were fed a high fat diet with ad libitum consumption of glucose and fructose in physiologically relevant concentrations and compared to mice fed a chow diet and also to both parent strains. Results: Following initiation of the obesogenic diet, B6/129 mice developed obesity, insulin resistance, hypertriglyceridemia and increased LDL-cholesterol. They sequentially also developed steatosis (4-8 weeks), steatohepatitis (16-24 weeks), progressive fibrosis (16 weeks onwards) and spontaneous hepatocellular cancer (HCC). There was a strong concordance between the pattern of pathway activation at a transcriptomic level between humans and mice with similar histological phenotypes (FDR 0.02 for early and 0.08 for late time points). Lipogenic, inflammatory and apoptotic signaling pathways activated in human NASH were also activated in these mice. The HCC gene signature resembled the S1 and S2 human subclasses of HCC (FDR 0.01 for both). Only the B6/129 mouse but not the parent strains recapitulated all of these aspects of human NAFLD. Conclusions: We here describe a diet-induced animal model of non-alcoholic fatty liver disease (DIAMOND) that recapitulates the key physiological, metabolic, histologic, transcriptomic and cell-signaling changes seen in humans with progressive NASH. Lay summary: We have developed a diet-induced mouse model of non-alcoholic steatohepatitis (NASH) and hepatic cancers in a cross between two mouse strains (129S1/SvImJ and C57Bl/6J). This model mimics all the physiological, metabolic, histological, transcriptomic gene signature and clinical endpoints of human NASH and can facilitate preclinical development of therapeutic targets for NASH. (C) 2016 European Association for the Study of the Liver. Published by Elsevier B.V.

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