Microarray profiling of isolated abdominal subcutaneous adipocytes from obese vs non-obese Pima Indians: increased expression of inflammation-related genes

被引:193
作者
Lee, YH
Nair, S
Rousseau, E
Allison, DB
Page, GP
Tataranni, PA
Bogardus, C
Permana, PA
机构
[1] NIDDKD, Obes 7 Diabet clin Res Sect, Phoenix epidemiol & Clin Res Branch, NIH, Phoenix, AZ USA
[2] Univ Alabama Birmingham, Dept Biostat, Sect Stat Genet, Birmingham, AL 35294 USA
[3] Univ Alabama Birmingham, Clin Nutr Res Ctr, Birmingham, AL 35294 USA
[4] Carl T hayden Vet Affairs Med Ctr, Phoenix, AZ 85012 USA
关键词
adipocyte; adipose tissue; gene expression; inflammation; microarray; obesity;
D O I
10.1007/s00125-005-1867-3
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims/hypothesis: Obesity increases the risk of developing major diseases such as diabetes and cardiovascular disease. Adipose tissue, particularly adipocytes, may play a major role in the development of obesity and its comorbidities. The aim of this study was to characterise, in adipocytes from obese people, the most differentially expressed genes that might be relevant to the development of obesity. Methods: We carried out microarray gene profiling of isolated abdominal subcutaneous adipocytes from 20 non-obese (BMI 25 +/- 3 kg/m(2)) and 19 obese (BMI 55 +/- 8 kg/m(2)) non-diabetic Pima Indians using Affymetrix HG-U95 GeneChip arrays. After data analyses, we measured the transcript levels of selected genes based on their biological functions and chromosomal positions using quantitative real-time PCR. Results: The most differentially expressed genes in adipocytes of obese individuals consisted of 433 upregulated and 244 downregulated genes. Of these, 410 genes could be classified into 20 functional Gene Ontology categories. The analyses indicated that the inflammation/ immune response category was over-represented, and that most inflammation-related genes were upregulated in adipocytes of obese subjects. Quantitative real-time PCR confirmed the transcriptional upregulation of representative inflammation-related genes (CCL2 and CCL3) encoding the chemokines monocyte chemoattractant protein-1 and macrophage inflammatory protein 1 alpha. The differential expression levels of eight positional candidate genes, including inflammation-related THY1 and C1QTNF5, were also confirmed. These genes are located on chromosome 11q22 - q24, a region with linkage to obesity in the Pima Indians. Conclusions/interpretation: This study provides evidence supporting the active role of mature adipocytes in obesity-related inflammation. It also provides potential candidate genes for susceptibility to obesity.
引用
收藏
页码:1776 / 1783
页数:8
相关论文
共 38 条
[1]   A mixture model approach for the analysis of microarray gene expression data [J].
Allison, DB ;
Gadbury, GL ;
Heo, MS ;
Fernández, JR ;
Lee, CK ;
Prolla, TA ;
Weindruch, R .
COMPUTATIONAL STATISTICS & DATA ANALYSIS, 2002, 39 (01) :1-20
[2]   Hunting for human obesity genes? Look in the adipose tissue! [J].
Arner, P .
INTERNATIONAL JOURNAL OF OBESITY, 2000, 24 (Suppl 4) :S57-S62
[3]   Adipose tissue compartments and insulin resistance in overweight-obese Caucasian men [J].
Chan, DC ;
Watts, GF ;
Sussekov, AV ;
Barrett, PHR ;
Yang, ZJ ;
Hua, JM ;
Song, ST .
DIABETES RESEARCH AND CLINICAL PRACTICE, 2004, 63 (02) :77-85
[4]   Weight loss regulates inflammation-related genes in white adipose tissue of obese subjects [J].
Clément, K ;
Viguerie, N ;
Poitou, C ;
Carette, C ;
Pelloux, V ;
Curat, CA ;
Sicard, A ;
Rome, S ;
Benis, A ;
Zucker, JD ;
Vidal, H ;
Laville, M ;
Barsh, GS ;
Basdevant, A ;
Stich, V ;
Cancello, R ;
Langin, D .
FASEB JOURNAL, 2004, 18 (14) :1657-1669
[5]   Regulation of adipocytokines and insulin resistance [J].
Fasshauer, M ;
Paschke, R .
DIABETOLOGIA, 2003, 46 (12) :1594-1603
[6]   Power and sample size estimation in high dimensional biology [J].
Gadbury, GL ;
Page, GP ;
Edwards, J ;
Kayo, T ;
Prolla, TA ;
Weindruch, R ;
Permana, PA ;
Mountz, JD ;
Allison, DB .
STATISTICAL METHODS IN MEDICAL RESEARCH, 2004, 13 (04) :325-338
[7]   Gene expression profile of omental adipose tissue in human obesity [J].
Gómez-Ambrosi, J ;
Catalán, V ;
Diez-Caballero, A ;
Martínez-Cruz, LA ;
Gil, MJ ;
García-Foncillas, J ;
Cienfuegoas, JA ;
Salvador, J ;
Mato, JM ;
Fruhbeck, G .
FASEB JOURNAL, 2004, 18 (01) :215-+
[8]   An autosomal genomic scan for loci linked to type II diabetes mellitus and body-mass index in Pima Indians [J].
Hanson, RL ;
Ehm, MG ;
Pettitt, DJ ;
Prochazka, M ;
Thompson, DB ;
Timberlake, D ;
Foroud, T ;
Kobes, S ;
Baler, L ;
Burns, DK ;
Almasy, L ;
Blangero, J ;
Garvey, WT ;
Bennett, PH ;
Knowler, WC .
AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 63 (04) :1130-1138
[9]   Endocrinology of adipose tissue [J].
Hauner, H ;
Hochberg, Z .
HORMONE AND METABOLIC RESEARCH, 2002, 34 (11-12) :605-606
[10]   Annotating the human proteome:: the Human Proteome Survey Database (HumanPSD™) and an in-depth target database for G protein-coupled receptors (GPCR-PD™) from Incyte Genomics [J].
Hodges, PE ;
Carrico, PM ;
Hogan, JD ;
O'Neill, KE ;
Owen, JJ ;
Mangan, M ;
Davis, BP ;
Brooks, JE ;
Garrels, JI .
NUCLEIC ACIDS RESEARCH, 2002, 30 (01) :137-141