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
[1]  
AaltoSetala K, 1996, J LIPID RES, V37, P1802
[2]  
[Anonymous], [No title captured]
[3]  
Brasaemle DL, 1997, J LIPID RES, V38, P2249
[4]   QUANTIFICATION OF HUMAN PLASMA APOLIPOPROTEINS C-I, C-II, AND C-III BY RADIOIMMUNOASSAYS [J].
BREN, ND ;
RASTOGI, A ;
KOTTKE, BA .
MAYO CLINIC PROCEEDINGS, 1993, 68 (07) :657-664
[5]   Expression profiling of palmitate- and oleate-regulated genes provides novel insights into the effects of chronic lipid exposure on pancreatic β-cell function [J].
Busch, AK ;
Cordery, D ;
Denyer, GS ;
Biden, TJ .
DIABETES, 2002, 51 (04) :977-987
[6]   Modulation of molecular mechanisms involved in protein synthesis machinery as a new tool for the control of cell proliferation [J].
Caraglia, M ;
Budillon, A ;
Vitale, G ;
Lupoli, G ;
Tagliaferri, P ;
Abbruzzese, A .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 2000, 267 (13) :3919-3936
[7]   Sodium palmitate induces partial mitochondrial uncoupling and reactive oxygen species in rat pancreatic islets in vitro [J].
Carlsson, C ;
Borg, LAH ;
Welsh, N .
ENDOCRINOLOGY, 1999, 140 (08) :3422-3428
[8]   A common variant in the ABCA1 gene is associated with a lower risk for premature coronary heart disease in familial hypercholesterolaemia [J].
Cenarro, A ;
Artieda, M ;
Castillo, S ;
Mozas, P ;
Reyes, G ;
Tejedor, D ;
Alonso, R ;
Mata, P ;
Pocoví, M ;
Civeira, F .
JOURNAL OF MEDICAL GENETICS, 2003, 40 (03) :163-168
[9]   Human apolipoproteins A-I and A-II in cell cholesterol efflux - Studies with transgenic mice [J].
Chiesa, G ;
Parolini, C ;
Canavesi, M ;
Colombo, N ;
Sirtori, CR ;
Fumagalli, R ;
Franceschini, G ;
Bernini, F .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1998, 18 (09) :1417-1423
[10]   The oxidative modification hypothesis of atherogenesis: An overview [J].
Chisolm, GM ;
Steinberg, D .
FREE RADICAL BIOLOGY AND MEDICINE, 2000, 28 (12) :1815-1826