Literature DB >> 12716739

Adipose tissue is a major source of interleukin-1 receptor antagonist: upregulation in obesity and inflammation.

Cristiana E Juge-Aubry1, Emmanuel Somm, Vittorio Giusti, Agnès Pernin, Rachel Chicheportiche, Chantal Verdumo, Françoise Rohner-Jeanrenaud, Danielle Burger, Jean-Michel Dayer, Christoph A Meier.   

Abstract

The secreted form of the interleukin-1 receptor antagonist (IL-1Ra) is an acute-phase protein intervening in the counterregulation of inflammatory processes. We previously showed that this cytokine antagonist is upregulated in the serum of obese patients, correlating with BMI and insulin resistance. In this study, we examined the expression pattern of IL-1Ra and showed that it is highly expressed not only in liver and spleen, but also in white adipose tissue (WAT), where it is upregulated in obesity. In WAT of obese humans, IL-1Ra was also markedly increased. Moreover, human WAT explants secreted IL-1Ra into the medium, a process that could be stimulated fivefold by interferon-beta. Finally, lipopolysaccharide administration induced a long-lasting expression of IL-1Ra in mouse WAT, suggesting that adipose tissue is an important source of IL-1Ra in both obesity and inflammation. In summary, we demonstrated that WAT is one of the most important sources of IL-1Ra quantitatively, suggesting that this tissue could represent a novel target for anti-inflammatory treatment. Moreover, it can be speculated that IL-1Ra, whose production is markedly increased in WAT in obese individuals, contributes further to weight gain because of its endocrine and paracrine effects on the hypothalamus and adipocytes, respectively.

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Year:  2003        PMID: 12716739     DOI: 10.2337/diabetes.52.5.1104

Source DB:  PubMed          Journal:  Diabetes        ISSN: 0012-1797            Impact factor:   9.461


  88 in total

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Journal:  Diabetes       Date:  2010-02-25       Impact factor: 9.461

10.  Elevated levels of the anti-inflammatory interleukin-1 receptor antagonist precede the onset of type 2 diabetes: the Whitehall II study.

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