共 74 条
Temporal and tissue-specific requirements for T-lymphocyte IL-6 signalling in obesity-associated inflammation and insulin resistance
被引:67
作者:

Xu, Elaine
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机构:
Max Planck Inst Metab Res, Dept Neuronal Control Metab, D-50931 Cologne, Germany
Univ Hosp, Ctr Endocrinol Diabet & Prevent Med CEDP, D-50924 Cologne, Germany
Univ Cologne, Excellence Cluster Cellular Stress Responses Agin, D-50931 Cologne, Germany
Univ Cologne, Ctr Mol Med Cologne, D-50931 Cologne, Germany Max Planck Inst Metab Res, Dept Neuronal Control Metab, D-50931 Cologne, Germany

Pereira, Mafalda M. A.
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h-index: 0
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Max Planck Inst Metab Res, Dept Neuronal Control Metab, D-50931 Cologne, Germany
Univ Hosp, Ctr Endocrinol Diabet & Prevent Med CEDP, D-50924 Cologne, Germany
Univ Cologne, Excellence Cluster Cellular Stress Responses Agin, D-50931 Cologne, Germany
Univ Cologne, Ctr Mol Med Cologne, D-50931 Cologne, Germany Max Planck Inst Metab Res, Dept Neuronal Control Metab, D-50931 Cologne, Germany

Karakasilioti, Ismene
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Max Planck Inst Metab Res, Dept Neuronal Control Metab, D-50931 Cologne, Germany
Univ Hosp, Ctr Endocrinol Diabet & Prevent Med CEDP, D-50924 Cologne, Germany
Univ Cologne, Excellence Cluster Cellular Stress Responses Agin, D-50931 Cologne, Germany
Univ Cologne, Ctr Mol Med Cologne, D-50931 Cologne, Germany Max Planck Inst Metab Res, Dept Neuronal Control Metab, D-50931 Cologne, Germany

Theurich, Sebastian
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Max Planck Inst Metab Res, Dept Neuronal Control Metab, D-50931 Cologne, Germany
Univ Hosp, Ctr Endocrinol Diabet & Prevent Med CEDP, D-50924 Cologne, Germany
Univ Cologne, Excellence Cluster Cellular Stress Responses Agin, D-50931 Cologne, Germany
Univ Cologne, Ctr Mol Med Cologne, D-50931 Cologne, Germany Max Planck Inst Metab Res, Dept Neuronal Control Metab, D-50931 Cologne, Germany

Al-Maarri, Mona
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Max Planck Inst Metab Res, Dept Neuronal Control Metab, D-50931 Cologne, Germany
Univ Hosp, Ctr Endocrinol Diabet & Prevent Med CEDP, D-50924 Cologne, Germany
Univ Cologne, Excellence Cluster Cellular Stress Responses Agin, D-50931 Cologne, Germany
Univ Cologne, Ctr Mol Med Cologne, D-50931 Cologne, Germany Max Planck Inst Metab Res, Dept Neuronal Control Metab, D-50931 Cologne, Germany

Rappl, Gunter
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Univ Cologne, Ctr Mol Med Cologne, D-50931 Cologne, Germany
Univ Cologne, Dept Internal Med 1, D-50931 Cologne, Germany Max Planck Inst Metab Res, Dept Neuronal Control Metab, D-50931 Cologne, Germany

Waisman, Ari
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Johannes Gutenberg Univ Mainz, Univ Med Ctr, Inst Mol Med, D-55131 Mainz, Germany Max Planck Inst Metab Res, Dept Neuronal Control Metab, D-50931 Cologne, Germany

Wunderlich, F. Thomas
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Max Planck Inst Metab Res, Dept Neuronal Control Metab, D-50931 Cologne, Germany
Univ Hosp, Ctr Endocrinol Diabet & Prevent Med CEDP, D-50924 Cologne, Germany
Univ Cologne, Excellence Cluster Cellular Stress Responses Agin, D-50931 Cologne, Germany
Univ Cologne, Ctr Mol Med Cologne, D-50931 Cologne, Germany Max Planck Inst Metab Res, Dept Neuronal Control Metab, D-50931 Cologne, Germany

Bruening, Jens C.
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h-index: 0
机构:
Max Planck Inst Metab Res, Dept Neuronal Control Metab, D-50931 Cologne, Germany
Univ Hosp, Ctr Endocrinol Diabet & Prevent Med CEDP, D-50924 Cologne, Germany
Univ Cologne, Excellence Cluster Cellular Stress Responses Agin, D-50931 Cologne, Germany
Univ Cologne, Ctr Mol Med Cologne, D-50931 Cologne, Germany
Natl Ctr Diabet Res DZD, D-85764 Neuherberg, Germany Max Planck Inst Metab Res, Dept Neuronal Control Metab, D-50931 Cologne, Germany
机构:
[1] Max Planck Inst Metab Res, Dept Neuronal Control Metab, D-50931 Cologne, Germany
[2] Univ Hosp, Ctr Endocrinol Diabet & Prevent Med CEDP, D-50924 Cologne, Germany
[3] Univ Cologne, Excellence Cluster Cellular Stress Responses Agin, D-50931 Cologne, Germany
[4] Univ Cologne, Ctr Mol Med Cologne, D-50931 Cologne, Germany
[5] Univ Cologne, Dept Internal Med 1, D-50931 Cologne, Germany
[6] Johannes Gutenberg Univ Mainz, Univ Med Ctr, Inst Mol Med, D-55131 Mainz, Germany
[7] Natl Ctr Diabet Res DZD, D-85764 Neuherberg, Germany
关键词:
SOLUBLE INTERLEUKIN-6 RECEPTOR;
FATTY LIVER-DISEASE;
ADIPOSE-TISSUE;
IN-VIVO;
METABOLIC DISEASE;
INTERFERON-GAMMA;
CELLS;
MICE;
MACROPHAGES;
ACTIVATION;
D O I:
10.1038/ncomms14803
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
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-alpha (IL-6R alpha(T-KO)) exposed to a HFD display improved glucose tolerance, insulin sensitivity and inflammation in liver and EWATafter 8 weeks. However, after 16 weeks, insulin resistance in IL-6R alpha(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.
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机构: IST RIC BIOL MOLEC P ANGELETTI, I-00040 POMEZIA, ROME, ITALY

Poli, V
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Rose-John, Stefan
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机构:
Univ Kiel, Dept Biochem, Biochem, D-24098 Kiel, Germany Univ Kiel, Dept Biochem, Biochem, D-24098 Kiel, Germany