Acute-Phase Serum Amyloid A as a Marker of Insulin Resistance in Mice

Metabolic;代谢免疫分析;MSD;代谢/内分泌
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Scheja, L., Hesse, B., Heike, Z., Michael, M.D., Siesky, A.M., Pospisil, H, Beisiegel, U., Seedorf, K.

  • Experimental Diabetes Research.
  • 2008
  • 2008:230837.
  • Canine,Human,Mouse,Non-Human Primate,Rat
  • MSD
  • Plasma
  • 免疫/内分泌
  • 胰岛素抵抗
  • Insulin

相关货号

LXMC04-1LXMH02-1LXMH03-4LXMH04-7LXMH07-3LXMH07-5LXMH07-7LXMH07-8LXMH10-9LXMH111-1LXMH22-1LXMH87-1LXMM02-2LXMM02-3LXMM03-2LXMM03-3LXMM06-2LXMM06-3LXMM06-4LXMM08-1LXMM10-3LXMM13-1LXMM58-1LXMN06-2LXMR02-2LXMR02-3LXMR03-3LXMR03-4LXMR06-1LXMR06-2LXMR07-1LXMR12-1

Abstract

Acute-phase serum amyloid A (A-SAA) was shown recently to correlate with obesity and insulin resistance in humans. However, the mechanisms linking obesity-associated inflammation and elevated plasma A-SAA to insulin resistance are poorly understood. Using high-fat diet- (HFD-) fed mice, we found that plasma A-SAA was increased early upon HFD feeding and was tightly associated with systemic insulin resistance. Plasma A-SAA elevation was due to induction of Saa1 and Saa2 expression in liver but not in adipose tissue. In adipose tissue Saa3 was the predominant isoform and the earliest inflammatory marker induced, suggesting it is important for initiation of adipose tissue inflammation. To assess the potential impact of A-SAA on adipose tissue insulin resistance, we treated 3T3-L1 adipocytes with recombinant A-SAA. Intriguingly, physiological levels of A-SAA caused alterations in gene expression closely resembling those observed in HFD-fed mice. Proinflammatory genes (Ccl2, Saa3) were induced while genes critical for insulin sensitivity (Irs1, Adipoq, Glut4) were down-regulated. Our data identify HFD-fed mice as a suitable model to study A-SAA as a biomarker and a novel possible mediator of insulin resistance.
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