A Microarray search for genes predominantly expressed in human omental adipocytes:: Adipose tissue as a major production site of serum amyloid A

被引:130
作者
Sjöholm, K
Palming, J
Olofsson, LE
Gummesson, A
Svensson, PA
Lystig, TC
Jennische, E
Brandberg, J
Torgerson, JS
Carlsson, B
Carlsson, LMS
机构
[1] Sahlgrens Univ Hosp, Res Ctr Endocrinol & Metab, Div Body Composit & Metab, Dept Internal Med, SE-41345 Gothenburg, Sweden
[2] Sahlgrens Univ Hosp, Res Ctr Endocrinol & Metab, Div Body Composit & Metab, Dept Radiol, SE-41345 Gothenburg, Sweden
[3] Univ Gothenburg, Sahlgrenska Acad, SE-41345 Gothenburg, Sweden
关键词
D O I
10.1210/jc.2004-1830
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
To identify genes predominantly expressed in omental adipocytes, microarray expression profiles from 33 human tissues or cell types were analyzed, using an algorithm developed for identification of transcripts predominantly expressed in a certain tissue. Both known adipocyte-specific and more unexpected genes were among the 28 genes identified. To validate the approach, adipocyte expression of three of these genes, acute-phase serum amyloid A (A-SAA), aquaporin 7, and transport secretion protein-2.2, was compared with 17 other human tissues by real-time PCR. The unexpectedly high expression of A-SAA in adipocytes was further verified by Northern blot and immunohistochemistry. The liver, reported to be the main production site for A-SAA, displayed the second highest expression using microarray and real-time PCR. In obese subjects, adipose tissue mRNA and serum A-SAA levels were down-regulated during an 18-wk diet regime (P < 0.05 and P < 0.0001, respectively). A-SAA serum levels were highly correlated to adipose tissue mRNA levels (P < 0.001) and to the total (P < 0.0001) and sc (P < 0.0001) adipose tissue areas, as analyzed by computed tomography. We show that adipose tissue is a major expression site of A-SAA during the nonacute-phase reaction condition. This provides a direct link between adipose tissue mass and a marker for low-grade inflammation and cardiovascular risk.
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页码:2233 / 2239
页数:7
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