Myeloid Sirtuin 6 Deficiency Causes Insulin Resistance in High-Fat Diet–Fed Mice by Eliciting Macrophage Polarization Toward an M1 Phenotype
Autor: | Byung-Hyun Park, Youngyi Lee, So-Young Park, Sun-O Ka, Yu-Na Chae, Eun Ju Bae, Mi-Kyung Kim, Hye-Na Cha |
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Rok vydání: | 2017 |
Předmět: |
0301 basic medicine
medicine.medical_specialty Endocrinology Diabetes and Metabolism Insulin medicine.medical_treatment Adipose tissue macrophages Macrophage polarization Adipose tissue Inflammation Biology medicine.disease Proinflammatory cytokine 03 medical and health sciences 030104 developmental biology Endocrinology Cytokine Insulin resistance Internal medicine Internal Medicine medicine medicine.symptom |
Zdroj: | Diabetes. 66:2659-2668 |
ISSN: | 1939-327X 0012-1797 |
DOI: | 10.2337/db16-1446 |
Popis: | Obesity-related insulin resistance is closely associated with macrophage accumulation and subsequent cytokine release in local tissues. Sirtuin 6 (Sirt6) is known to exert an anti-inflammatory function, but its role in macrophages in the context of obesity has not been investigated. We generated myeloid-specific Sirt6 knockout (mS6KO) mice and investigated the metabolic characteristics after high-fat diet (HFD) feeding for 16 weeks. Compared with their wild-type littermates, HFD-fed mS6KO mice exhibited greater increases in body weight, fasting blood glucose and insulin levels, hepatic steatosis, glucose intolerance, and insulin resistance. Gene expression, histology, and flow cytometric analyses demonstrated that liver and adipose tissue inflammation were elevated in HFD-fed mS6KO mice relative to wild type, with a greater accumulation of F4/80+CD11b+CD11c+ adipose tissue macrophages. Myeloid Sirt6 deletion facilitated proinflammatory M1 polarization of bone marrow macrophages and augmented the migration potential of macrophages toward adipose-derived chemoattractants. Mechanistically, Sirt6 deletion in macrophages promoted the activation of nuclear factor-κB (NF-κB) and endogenous production of interleukin-6, which led to STAT3 activation and the positive feedback circuits for NF-κB stimulation; this cross talk expedited an M1 polarization. We conclude that Sirt6 in macrophages is required for the prevention of obesity-associated tissue inflammation and insulin resistance. |
Databáze: | OpenAIRE |
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