Correlation Analysis Between Gene Expression Profile of Rat Liver Tissues and High-Fat Emulsion-Induced Nonalcoholic Fatty Liver

被引:34
作者
Xu, Cunshuan [1 ,2 ]
Wang, Gaiping [1 ]
Hao, Yunpeng [1 ]
Zhi, Jia [1 ]
Zhang, Lianxing [2 ]
Chang, Cuifang [2 ]
机构
[1] Henan Normal Univ, Coll Life Sci, Xinxiang 453007, Henan, Peoples R China
[2] Key Lab Cell Differentiat Regulat, Xinxiang 453007, Henan, Peoples R China
关键词
NAFLD; NASH; Gene expression profile; Systems biology; Physiological activity; KUPFFER CELLS; ACID; DISEASE; METABOLISM; STEATOHEPATITIS; INFLAMMATION; MECHANISMS; APOPTOSIS; LIPOLYSIS; ALPHA;
D O I
10.1007/s10620-011-1599-9
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background Nonalcoholic fatty liver disease (NAFLD) is caused by fat metabolism disorders and thereby abnormal or excessive accumulation of fat in hepatocytes, and characterized by steatosis, inflammation, fibrosis, apoptosis or necrosis. Aim This study was carried out to explore the correlation between gene expression profiles of rat livers and the occurrence and progression of NAFLD at the transcriptional level. Methods A rat model of nonalcoholic steatohepatitis (NASH) was established by feeding male rats with high-fat emulsion via gavage, and Rat Genome 230 2.0 Array was used to detect gene expression profiles of liver tissues obtained from male rats following 0, 2, 4, and 6 weeks of high-fat emulsion feeding. Methods of bioinformatics and systems biology were applied to analyze the correlation between gene expression changes and physiological activities involved in NAFLD. Results In total, 93 function-known genes, including 36 up-regulated and 57 down-regulated, differed significantly in expression compared to those of control rats, and 18 physiological activities were closely related to NAFLD. Especially, the activity of cell differentiation was decreased during the whole process of NAFLD, and the activities of inflammation response, stimulus response, cell migration and adhesion were attenuated in the second, fourth and sixth week, respectively. In the fourth and sixth weeks, lipid metabolism and cell apoptosis were augmented, and the former might be associated with the enhanced expression of plin, acsl6, scd2, elovl3, etc. Conclusions These data provide useful information on the global gene expression changes due to high-fat emulsion feeding and bring important insights into the mechanisms of NAFLD.
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收藏
页码:2299 / 2308
页数:10
相关论文
共 37 条
[11]   Gender differences in the insulin-like growth factor axis response to a glucose load [J].
Flanagan, D. E. ;
Holt, R. I. G. ;
Owens, P. C. ;
Cockington, R. J. ;
Moore, V. M. ;
Robinson, J. S. ;
Godsland, I. F. ;
Phillips, D. I. W. .
ACTA PHYSIOLOGICA, 2006, 187 (03) :371-378
[12]   Gene expression in human NAFLD [J].
Greco, Dario ;
Kotronen, Anna ;
Westerbacka, Jukka ;
Puig, Oscar ;
Arkkila, Perttu ;
Kiviluoto, Tuula ;
Laitinen, Saara ;
Kolak, Maria ;
Fisher, Rachel M. ;
Hamsten, Anders ;
Auvinen, Petri ;
Yki-Jarvinen, Hannele .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2008, 294 (05) :G1281-G1287
[13]   Expression profiles of the organic acid metabolism-associated genes during rat liver regeneration [J].
Guo, G. B. ;
Xu, C. S. .
AMINO ACIDS, 2008, 34 (04) :597-604
[14]   Systemic inflammation in nonalcoholic fatty liver disease is characterized by elevated levels of CCL2 [J].
Haukeland, John Willy ;
Damas, Jan Kristian ;
Konopski, Zbigniew ;
Loberg, Else Marit ;
Haaland, Terese ;
Goverud, Ingeborg ;
Torjesen, Peter A. ;
Birkeland, Kare ;
Bjoro, Kristian ;
Aukrust, Pal .
JOURNAL OF HEPATOLOGY, 2006, 44 (06) :1167-1174
[15]   Involvement of preprotachykinin A gene-encoded peptides and the neurokinin 1 receptor in endotoxin-induced murine airway inflammation [J].
Helyes, Zsuzsanna ;
Elekes, Krisztian ;
Sandor, Katalin ;
Szitter, Istvan ;
Kereskai, Laszlo ;
Pinter, Erika ;
Kemeny, Agnes ;
Szolcsanyi, Janos ;
McLaughlin, Lynn ;
Vasiliou, Sylvia ;
Kipar, Anja ;
Zimmer, Andreas ;
Hunt, Stephen P. ;
Stewart, James P. ;
Quinn, John P. .
NEUROPEPTIDES, 2010, 44 (05) :399-406
[16]   Mechanisms of Disease Progression in Nonalcoholic Fatty Liver Disease [J].
Jou, Janice ;
Choi, Steve S. ;
Diehl, Anna Mae .
SEMINARS IN LIVER DISEASE, 2008, 28 (04) :370-379
[17]   CYTOKINE GENE-EXPRESSION BY KUPFFER CELLS IN EXPERIMENTAL ALCOHOLIC LIVER-DISEASE [J].
KAMIMURA, S ;
TSUKAMOTO, H .
HEPATOLOGY, 1995, 22 (04) :1304-1309
[18]  
Kohjima M, 2007, INT J MOL MED, V20, P351
[19]   Liver glucokinase gene expression is controlled by the onecut transcription factor hepatocyte nuclear factor-6 [J].
Lannoy, VJ ;
Decaux, JF ;
Pierreux, CE ;
Lemaigre, FP ;
Rousseau, GG .
DIABETOLOGIA, 2002, 45 (08) :1136-1141
[20]   Regulation of hepatic lipogenesis by the transcription factor XBP1 [J].
Lee, Ann-Hwee ;
Scapa, Erez F. ;
Cohen, David E. ;
Glimcher, Laurie H. .
SCIENCE, 2008, 320 (5882) :1492-1496