Serum proteomic analysis of diet-induced steatohepatitis and metabolic syndrome in the Ossabaw miniature swine

被引:51
|
作者
Bell, Lauren N. [1 ,2 ]
Lee, Lydia [1 ]
Saxena, Romil [1 ,3 ]
Bemis, Kerry G.
Wang, Mu [4 ]
Theodorakis, Janice L.
Vuppalanchi, Raj [1 ,2 ]
Alloosh, Mouhamad [5 ]
Sturek, Michael [5 ]
Chalasani, Naga [1 ,2 ]
机构
[1] Indiana Univ, Sch Med, Div Gastroenterol Hepatol, Indianapolis, IN 46202 USA
[2] Indiana Univ, Sch Med, Div Clin Pharmacol, Indianapolis, IN 46202 USA
[3] Indiana Univ, Sch Med, Dept Pathol & Lab Med, Indianapolis, IN 46202 USA
[4] Indiana Univ, Sch Med, Dept Biochem & Mol Biol, Indianapolis, IN 46202 USA
[5] Indiana Univ, Sch Med, Dept Cellular & Integrat Physiol, Indianapolis, IN 46202 USA
基金
美国国家卫生研究院;
关键词
mass spectrometry; fatty liver disease; nonalcoholic steatohepatitis; animal model; fibrosis; NONALCOHOLIC FATTY LIVER; MASS-SPECTROMETRY; PROTEIN; QUANTIFICATION; DISEASE; FIBROSIS; TANDEM;
D O I
10.1152/ajpgi.00485.2009
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Bell LN, Lee L, Saxena R, Bemis KG, Wang M, Theodorakis JL, Vuppalanchi R, Alloosh M, Sturek M, Chalasani N. Serum proteomic analysis of diet-induced steatohepatitis and metabolic syndrome in the Ossabaw miniature swine. Am J Physiol Gastrointest Liver Physiol 298: G746-G754, 2010. First published February 18, 2010; doi:10.1152/ajpgi.00485.2009.-We recently developed a nutritional model of steatohepatitis and metabolic syndrome in Ossabaw pigs. Here we describe changes in the serum proteome of pigs fed standard chow (control group; n = 7), atherogenic diet (n = 5), or modified atherogenic diet (M-ath diet group; n = 6). Pigs fed atherogenic diet developed metabolic syndrome and mildly abnormal liver histology, whereas pigs fed M-ath diet exhibited severe metabolic syndrome and liver injury closely resembling human nonalcoholic steatohepatitis (NASH). Using a label-free mass spectrometry-based proteomics approach, we identified 1,096 serum proteins, 162 of which changed significantly between any two diet groups (false discovery rate <5%). Biological classification of proteins with significant changes revealed functions previously implicated in development of NASH in humans, including immune system regulation and inflammation (orosomucoid 1, serum amyloid P component, paraoxonase 1, protein similar to alpha-2-macroglobulin precursor, beta-2-microglobulin, p101 protein, and complement components 2 and C8G), lipid metabolism (apolipoproteins C-III, E, E precursor, B, and N), structural and extracellular matrix proteins (transthyretin and endopeptidase 24.16 type M2), and coagulation [carboxypeptidase B2 (plasma)]. Several proteins with significant differential expression in pigs were also identified in our recent human proteomics study as changing significantly in serum from patients across the spectrum of nonalcoholic fatty liver disease, including apolipoproteins C-III and B, orosomucoid 1, serum amyloid P component, transthyretin, paraoxonase 1, and a protein similar to alpha-2-macroglobulin precursor. This serum proteomic analysis provides additional information about the pathogenesis of NASH and further characterizes our large animal model of diet-induced steatohepatitis and metabolic syndrome in Ossabaw pigs.
引用
收藏
页码:G746 / G754
页数:9
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