Temporal and tissue-specific requirements for T-lymphocyte IL-6 signalling in obesity-associated inflammation and insulin resistance

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作者
Elaine Xu
Mafalda M. A. Pereira
Ismene Karakasilioti
Sebastian Theurich
Mona Al-Maarri
Gunter Rappl
Ari Waisman
F. Thomas Wunderlich
Jens C. Brüning
机构
[1] Max Planck Institute for Metabolism Research,Department of Neuronal Control of Metabolism
[2] Center for Endocrinology,Center for Molecular Medicine Cologne (CMMC) and Department of Internal Medicine I
[3] Diabetes and Preventive Medicine (CEDP),undefined
[4] University Hospital,undefined
[5] Excellence Cluster on Cellular Stress Responses in Aging Associated Diseases (CECAD) and Center of Molecular Medicine Cologne (CMMC),undefined
[6] University of Cologne,undefined
[7] University of Cologne,undefined
[8] Institute for Molecular Medicine,undefined
[9] University of Medical Centre of the Johannes Gutenberg University of Mainz,undefined
[10] National Center for Diabetes Research (DZD),undefined
来源
Nature Communications | / 8卷
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摘要
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-α (IL-6RαT-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-6RαT-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.
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