Feeding conditions control the expression of genes involved in sterol metabolism in peripheral blood mononuclear cells of normoweight and diet-induced (cafeteria) obese rats

被引:38
作者
Caimari, Antoni [1 ,2 ]
Oliver, Paula [1 ,2 ]
Rodenburg, Wendy [3 ,4 ]
Keijer, Jaap [3 ]
Palou, Andreu [1 ,2 ]
机构
[1] Univ Illes Balears, Lab Mol Biol Nutr & Biotechnol, E-07122 Palma de Mallorca, Spain
[2] CIBER Fisiopatol Obesidad & Nutr CIBEROBN, E-07122 Palma de Mallorca, Spain
[3] Wageningen Univ, NL-6708 PG Wageningen, Netherlands
[4] RIKILT Inst Food Safety, Food Bioact Grp, NL-6708 PD Wageningen, Netherlands
关键词
PBMC; Microarray; Sterol metabolism; Cafeteria diet; Feeding conditions; LOW-DENSITY-LIPOPROTEIN; ACUTE REGULATORY PROTEIN; COA-CHOLESTEROL ACYLTRANSFERASE; BETA-METHYLGLUTARYL-COENZYME; MESSENGER-RNA EXPRESSION; SIGNAL-TRANSDUCTION; HUMAN-LYMPHOCYTES; LIPID-SYNTHESIS; ADIPOSE-TISSUE; IN-VIVO;
D O I
10.1016/j.jnutbio.2009.10.001
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
Peripheral blood mononuclear cells (PBMC) are easily obtainable cells from blood whose gene expression profiles have been proven to be highly robust in distinguishing a disease state from healthy state. Sterol metabolism is of physiological importance, and although its nutritional response in liver has been described, it is poorly studied in PBMC. To examine if PBMC sterol metabolism reflects diet-induced physiological responses, we analysed the whole genome gene expression response of PBMC and focused on sterol metabolism-related genes affected by different feeding conditions (ad libitum feeding, fasting, and refeeding) in normoweight (control) rats and in diet-induced (cafeteria) obese rats. Our results of microarray analysis show that, in control rats, 21 genes involved in sterol metabolism were regulated by the different feeding conditions, whereas in cafeteria-obese rats, only seven genes showed a changed expression. Most of the genes identified were classified into three pathways: sterol biosynthesis, cholesterol transport and uptake and sterol signaling. The expression profile of these genes was similar to that previously described for liver, decreasing in response to fasting conditions and recovering the levels found in fed animals after 6-h-refeeding. In addition, our data and the comparable expression pattern of sterol metabolism-related genes between PBMC and liver suggest similar sterol regulatory element-binding protein-mediated regulatory mechanisms in response to feeding conditions in both tissues. In conclusion, the expression of genes involved in sterol metabolism is highly controlled by feeding conditions in PBMC of control rats, but this control is impaired in cafeteria-obese animals. The pathophysiological significance of this impairment requires further investigation. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:1127 / 1133
页数:7
相关论文
共 70 条
[1]   Microarray data analysis: from disarray to consolidation and consensus [J].
Allison, DB ;
Cui, XQ ;
Page, GP ;
Sabripour, M .
NATURE REVIEWS GENETICS, 2006, 7 (01) :55-65
[2]   Identification of a form of acyl-CoA:cholesterol acyltransferase specific to liver and intestine in nonhuman primates [J].
Anderson, RA ;
Joyce, C ;
Davis, M ;
Reagan, JW ;
Clark, M ;
Shelness, GS ;
Rudel, LL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (41) :26747-26754
[3]   Phosphorylation of steroidogenic acute regulatory protein (StAR) modulates its steroidogenic activity [J].
Arakane, F ;
King, SR ;
Du, Y ;
Kallen, CB ;
Walsh, LP ;
Watari, H ;
Stocco, DM ;
Strauss, JF .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (51) :32656-32662
[4]  
Batetta B, 2002, CELL PROLIFERAT, V35, P143
[5]   ST7 is a novel low-density lipoprotein receptor-related protein (LRP) with a cytoplasmic tail that interacts with proteins related to signal transduction pathways [J].
Battle, MA ;
Maher, VM ;
McCormick, JJ .
BIOCHEMISTRY, 2003, 42 (24) :7270-7282
[6]   SREBP in signal transduction: cholesterol metabolism and beyond [J].
Bengoechea-Alonso, Maria T. ;
Ericsson, Johan .
CURRENT OPINION IN CELL BIOLOGY, 2007, 19 (02) :215-222
[7]   Selective binding of sterol regulatory element-binding protein isoforms and co-regulatory proteins to promoters for lipid metabolic genes in liver [J].
Bennett, Mary K. ;
Datta, Young-Kyo Seo Shrimati ;
Shin, Dong-Ju ;
Osborne, Timothy F. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2008, 283 (23) :15628-15637
[8]   BIOLOGICAL SYNTHESIS OF CHOLESTEROL [J].
BLOCH, K .
SCIENCE, 1965, 150 (3692) :19-&
[9]   Resistin, an adipokine with potent proinflammatory properties [J].
Bokarewa, M ;
Nagaev, I ;
Dahlberg, L ;
Smith, U ;
Tarkowski, A .
JOURNAL OF IMMUNOLOGY, 2005, 174 (09) :5789-5795
[10]   Activation of peroxisome proliferator-activated receptor alpha in human peripheral blood mononuclear cells reveals an individual gene expression profile response [J].
Bouwens, Mark ;
Afman, Lydia A. ;
Muller, Michael .
BMC GENOMICS, 2008, 9 (1)