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.
引用
收藏
页码:2299 / 2308
页数:10
相关论文
共 37 条
[1]   Rac1 links integrin-mediated adhesion to the control of lactational differentiation in mammary epithelia [J].
Akhtar, Nasreen ;
Streuli, Charles H. .
JOURNAL OF CELL BIOLOGY, 2006, 173 (05) :781-793
[2]   Nonalcoholic fatty liver disease [J].
Brunt, Elizabeth M. ;
Wong, Vincent W. -S. ;
Nobili, Valerio ;
Day, Christopher P. ;
Sookoian, Silvia ;
Maher, Jacquelyn J. ;
Bugianesi, Elisabetta ;
Sirlin, Claude B. ;
Neuschwander-Tetri, BrentA. ;
Rinella, Mary E. .
NATURE REVIEWS DISEASE PRIMERS, 2015, 1
[3]   Threshold levels of hepatocyte nuclear factor 6 (HNF-6) acting in synergy with HNF-4 and PGC-1α are required for time-specific gene expression during liver development [J].
Beaudry, Jean-Bernard ;
Pierreux, Christophe E. ;
Hayhurst, Graham P. ;
Plumb-Rudewiez, Nicolas ;
Weiss, Mary C. ;
Rousseau, Guy G. ;
Lemaigre, Frederic P. .
MOLECULAR AND CELLULAR BIOLOGY, 2006, 26 (16) :6037-6046
[4]   Identification of a lipokine, a lipid hormone linking adipose tissue to systemic metabolism [J].
Cao, Haiming ;
Gerhold, Kristin ;
Mayers, Jared R. ;
Wiest, Michelle M. ;
Watkins, Steven M. ;
Hotamisligil, Goekhan S. .
CELL, 2008, 134 (06) :933-944
[5]  
Chen XG, 2010, GENOME, V53, P608, DOI [10.1139/G10-040, 10.1139/g10-040]
[6]   Ethanol and Arachidonic Acid Synergize to Activate Kupffer Cells and Modulate the Fibrogenic Response via Tumor Necrosis Factor α, Reduced Glutathione, and Transforming Growth Factor β-Dependent Mechanisms [J].
Cubero, Francisco Javier ;
Nieto, Natalia .
HEPATOLOGY, 2008, 48 (06) :2027-2039
[7]   Steatohepatitis: A tale of two "hits"? [J].
Day, CP ;
James, OFW .
GASTROENTEROLOGY, 1998, 114 (04) :842-845
[8]   Functional interaction of HTLV-1 Tax protein with the POZ domain of the transcriptional repressor BCL6 [J].
Dean, J. ;
Hashimoto, K. ;
Tsuji, T. ;
Gautier, V. ;
Hall, W. W. ;
Sheehy, N. .
ONCOGENE, 2009, 28 (42) :3723-3734
[9]  
Edmison John, 2007, Clin Liver Dis, V11, P75, DOI 10.1016/j.cld.2007.02.011
[10]   Hepatocyte apoptosis and Fas expression are prominent features of human nonalcoholic steatohepatitis [J].
Feldstein, AE ;
Canbay, A ;
Angulo, P ;
Taniai, M ;
Burgart, LJ ;
Lindor, KD ;
Gores, GJ .
GASTROENTEROLOGY, 2003, 125 (02) :437-443