8 research outputs found

    The inflammasome-mediated caspase-1 activation controls adipocyte differentiation and insulin sensitivity.

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    Contains fulltext : 87798.pdf (publisher's version ) (Closed access)Obesity-induced inflammation originating from expanding adipose tissue interferes with insulin sensitivity. Important metabolic effects have been recently attributed to IL-1beta and IL-18, two members of the IL-1 family of cytokines. Processing of IL-1beta and IL-18 requires cleavage by caspase-1, a cysteine protease regulated by a protein complex called the inflammasome. We demonstrate that the inflammasome/caspase-1 governs adipocyte differentiation and insulin sensitivity. Caspase-1 is upregulated during adipocyte differentiation and directs adipocytes toward a more insulin-resistant phenotype. Treatment of differentiating adipocytes with recombinant IL-1beta and IL-18, or blocking their effects by inhibitors, reveals that the effects of caspase-1 on adipocyte differentiation are largely conveyed by IL-1beta. Caspase-1 and IL-1beta activity in adipose tissue is increased both in diet-induced and genetically induced obese animal models. Conversely, mice deficient in caspase-1 are more insulin sensitive as compared to wild-type animals. In addition, differentiation of preadipocytes isolated from caspase-1(-/-) or NLRP3(-/-) mice resulted in more metabolically active fat cells. In vivo, treatment of obese mice with a caspase-1 inhibitor significantly increases their insulin sensitivity. Indirect calorimetry analysis revealed higher fat oxidation rates in caspase-1(-/-) animals. In conclusion, the inflammasome is an important regulator of adipocyte function and insulin sensitivity, and caspase-1 inhibition may represent a novel therapeutic target in clinical conditions associated with obesity and insulin resistance

    Annuaire du Collège de France 2013-2014

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    L’Annuaire du Collège de France 2013-2014. Résumé des cours et travaux 114e année est le reflet de l’activité scientifique de l’institution pour l’année académique 2013-2014. Il contient notamment les résumés détaillés des enseignements et une présentation des recherches menées par les professeurs du Collège de France, leurs laboratoires et équipes de recherche

    PDE4 inhibitors as new anti-inflammatory drugs: Effects on cell trafficking and cell adhesion molecules expression

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