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

Détails

ID Serval
serval:BIB_D5A74A71DEC0
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Adipose tissue is a major source of interleukin-1 receptor antagonist: upregulation in obesity and inflammation
Périodique
Diabetes
Auteur⸱e⸱s
Juge-Aubry  C. E., Somm  E., Giusti  V., Pernin  A., Chicheportiche  R., Verdumo  C., Rohner-Jeanrenaud  F., Burger  D., Dayer  J. M., Meier  C. A.
ISSN
0012-1797 (Print)
Statut éditorial
Publié
Date de publication
05/2003
Volume
52
Numéro
5
Pages
1104-10
Notes
Journal Article
Research Support, Non-U.S. Gov't --- Old month value: May
Résumé
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.
Mots-clé
Adipose Tissue/drug effects/*physiopathology Animals *Gene Expression Regulation Humans Inflammation/genetics/immunology Interferon-beta/pharmacology Interleukin 1 Receptor Antagonist Protein Mice Mice, Inbred C57BL Mice, Obese Obesity/genetics/*immunology Organ Culture Techniques RNA, Messenger/genetics Reference Values Sialoglycoproteins/drug effects/*genetics/secretion Tumor Necrosis Factor-alpha/genetics/physiology
Pubmed
Web of science
Open Access
Oui
Création de la notice
25/01/2008 16:22
Dernière modification de la notice
20/08/2019 15:55
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