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10.1038/ncomms14803

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suck abstract from ncbi


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pmid28466852
      Nat+Commun 2017 ; 8 (ä): 14803
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  • Temporal and tissue-specific requirements for T-lymphocyte IL-6 signalling in obesity-associated inflammation and insulin resistance #MMPMID28466852
  • Xu E ; Pereira MMA ; Karakasilioti I ; Theurich S ; Al-Maarri M ; Rappl G ; Waisman A ; Wunderlich FT ; Brüning JC
  • Nat Commun 2017[May]; 8 (ä): 14803 PMID28466852 show ga
  • Low-grade inflammation links obesity to insulin resistance through the activation of tissue-infiltrating immune cells. Interleukin-6 (IL-6) is a crucial regulator of T cells and is increased in obesity. Here we report that classical IL-6 signalling in T cells promotes inflammation and insulin resistance during the first 8 weeks on a high-fat diet (HFD), but becomes dispensable at later stages (after 16 weeks). Mice with T cell-specific deficiency of IL-6 receptor-? (IL-6R?(T-KO)) exposed to a HFD display improved glucose tolerance, insulin sensitivity and inflammation in liver and EWAT after 8 weeks. However, after 16 weeks, insulin resistance in IL-6R?(T-KO) epididymal white adipose tissue (EWAT) is comparable to that of controls, whereas the inflammatory profile is significantly worse. This coincided with a shift from classical T cell IL-6 signalling at 8 weeks, to enhanced IL-6 trans-signalling at 16 weeks. Collectively, our studies reveal that IL-6 action in T cells through classical IL-6 signalling promotes inflammation and insulin resistance early during obesity development, which can be compensated for by enhanced IL-6 trans-signalling at later stages.
  • |*Insulin Resistance [MESH]
  • |*Signal Transduction [MESH]
  • |Animals [MESH]
  • |Blood Glucose/metabolism [MESH]
  • |Diet, High-Fat [MESH]
  • |Homeostasis [MESH]
  • |Inflammation/*metabolism [MESH]
  • |Interleukin-6/genetics/*metabolism [MESH]
  • |Lipid Metabolism [MESH]
  • |Male [MESH]
  • |Mice [MESH]
  • |Mice, Knockout [MESH]
  • |Obesity/*metabolism [MESH]
  • |Receptors, Interleukin-6/genetics [MESH]
  • |T-Lymphocytes/*metabolism [MESH]


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