HVEM-deficient mice fed a high-fat diet are protected from adipose tissue inflammation and glucose intolerance
pmid: 21679708
HVEM-deficient mice fed a high-fat diet are protected from adipose tissue inflammation and glucose intolerance
HVEM is a member of the TNF receptor superfamily that plays a role in the development of various inflammatory diseases. In this study, we show that HVEM deficiency attenuates adipose tissue inflammatory responses and glucose intolerance in diet-induced obesity. Feeding a high-fat diet (HFD) to HVEM-deficient mice elicited a reduction in the number of macrophages and T cells infiltrated into adipose tissue. Proinflammatory cytokine levels in the adipose tissue decreased in HFD-fed HVEM-deficient mice, while levels of the anti-inflammatory cytokine IL-10 increased. Moreover, glucose intolerance and insulin sensitivity were markedly improved in the HFD-fed HVEM-deficient mice. These findings indicate that HVEM may be a useful target for combating obesity-induced inflammatory responses and insulin resistance.
- University of Ulsan Korea (Republic of)
- Kyoto University Japan
- University of Ulsan Korea (Republic of)
Blood Glucose, Inflammation, Adipose tissue, Insulin resistance, Dietary Fats, Mice, Adipose Tissue, Glucose Intolerance, Adipocytes, Animals, Cytokines, Insulin, Obesity, Insulin Resistance, Receptors, Tumor Necrosis Factor, Member 14
Blood Glucose, Inflammation, Adipose tissue, Insulin resistance, Dietary Fats, Mice, Adipose Tissue, Glucose Intolerance, Adipocytes, Animals, Cytokines, Insulin, Obesity, Insulin Resistance, Receptors, Tumor Necrosis Factor, Member 14
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