Expression analysis of a human hepatic cell line in response to palmitate

被引:23
作者
Swagell, CD
Henly, DC
Morris, CP
机构
[1] Queensland Univ Technol, Cooperat Res Ctr Diagnost, Brisbane, Qld 4001, Australia
[2] Univ Queensland, Sch Mol & Microbial Sci, St Lucia, Qld 4067, Australia
[3] Bond Univ, Sch Hlth Sci, Gold Coast, Qld 4229, Australia
关键词
cDNA microarray analysis; gene expression; saturated fatty acid; palmitate; hepatocytes;
D O I
10.1016/j.bbrc.2004.12.188
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Saturated fat plays a role in common debilitating diseases such as obesity, type 2 diabetes, and coronary heart disease. It is also clear that certain fatty acids act as regulators of metabolism via both direct and indirect signalling of target tissues. As the molecular mechanisms of saturated fatty acid signalling in the liver are poorly defined, hepatic gene expression analysis was undertaken in a human hepatocyte cell line after incubation with palmitate. Profiling of mRNA expression using cDNA microarray analysis revealed that 162 of approximately 18,000 genes tested were differentially expressed after incubation with palmitate for 48 h. Altered transcription profiles were observed in a wide variety of genes, including genes involved in lipid and cholesterol transport, cholesterol catabolism, cell growth and proliferation, cell signalling, P-oxidation, and oxidative stress response. While palinitate signalling has been examined in pancreatic beta-cells, this is the first report showing that palmitate regulates expression of numerous genes via direct molecular signalling mechanisms in liver cells. (C) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:432 / 441
页数:10
相关论文
共 37 条
[11]   Transcript profiling suggests that differential metabolic adaptation of mice to a high fat diet is associated with changes in liver to muscle lipid fluxes [J].
de Fourmestraux, V ;
Neubauer, H ;
Poussin, C ;
Farmer, P ;
Falquet, L ;
Burcelin, R ;
Delorenzi, M ;
Thorens, B .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (49) :50743-50753
[12]   Peroxisome proliferator-activated receptors: Nuclear control of metabolism [J].
Desvergne, B ;
Wahli, W .
ENDOCRINE REVIEWS, 1999, 20 (05) :649-688
[13]   Cytoprotection against oxidative stress and the regulation of glutathione synthesis [J].
Dickinson, DA ;
Moellering, DR ;
Iles, KE ;
Patel, RP ;
Levonen, AL ;
Wigley, A ;
Darley-Usmar, VM ;
Forman, HJ .
BIOLOGICAL CHEMISTRY, 2003, 384 (04) :527-537
[14]   Cell cycle checkpoints: Preventing an identity crisis [J].
Elledge, SJ .
SCIENCE, 1996, 274 (5293) :1664-1672
[15]   A ROLE FOR THE DYSTROPHIN-GLYCOPROTEIN COMPLEX AS A TRANSMEMBRANE LINKER BETWEEN LAMININ AND ACTIN [J].
ERVASTI, JM ;
CAMPBELL, KP .
JOURNAL OF CELL BIOLOGY, 1993, 122 (04) :809-823
[16]   Regulation of hepatic neutral cholesteryl ester hydrolase by hormones and changes in cholesterol flux [J].
Ghosh, S ;
Natarajan, R ;
Pandak, WM ;
Hylemon, PB ;
Grogan, WM .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 1998, 274 (04) :G662-G668
[17]   New atherosclerosis risk factors in obese, hypertensive and diabetic children and adolescents [J].
Glowinska, B ;
Urban, M ;
Koput, A ;
Galar, M .
ATHEROSCLEROSIS, 2003, 167 (02) :275-286
[18]   Are desmosomes more than tethers for intermediate filaments? [J].
Green, KJ ;
Gaudry, CA .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2000, 1 (03) :208-216
[19]  
Hardy S, 2000, CANCER RES, V60, P6353
[20]   The effects of insulin-like growth factors on tumorigenesis and neoplastic growth [J].
Khandwala, HM ;
McCutcheon, IE ;
Flyvbjerg, A ;
Friend, KE .
ENDOCRINE REVIEWS, 2000, 21 (03) :215-244