The PGC-1 coactivators promote an anti-inflammatory environment in skeletal muscle in vivo

被引:77
作者
Eisele, Petra Sabine [1 ,2 ]
Furrer, Regula [1 ]
Beer, Markus [1 ]
Handschin, Christoph [1 ,2 ]
机构
[1] Univ Basel, Biozentrum, Div Pharmacol Neurobiol, CH-4056 Basel, Switzerland
[2] Univ Zurich, Zurich Ctr Integrat Human Physiol, CH-8057 Zurich, Switzerland
基金
瑞士国家科学基金会;
关键词
Inflammation; PGC-1; Skeletal muscle; Metabolism; Mitochondria; NF-KAPPA-B; PGC-1-ALPHA; MACROPHAGES; INFLAMMATION; ACTIVATION; EXERCISE; OBESITY; MICE; EXPRESSION; REDUCTION;
D O I
10.1016/j.bbrc.2015.06.166
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
The peroxisome proliferator-activated receptor gamma coactivator 1 alpha (PGC-1 alpha) is abundantly expressed in trained muscles and regulates muscle adaptation to endurance exercise. Inversely, mice lacking a functional PGC-1 alpha allele in muscle exhibit reduced muscle functionality and increased inflammation. In isolated muscle cells, PGC-1 alpha and the related FCC-1 beta counteract the induction of inflammation by reducing the activity of the nuclear factor kappa B (NE kappa B). We now tested the effects of these metabolic regulators on inflammatory reactions in muscle tissue of control and muscle-specific PGC-1 alpha/-1 beta transgenic mice in vivo in the basal state as well as after an acute inflammatory insult. Surprisingly, we observed a PGC-1-dependent alteration of the cytokine profile characterized by an increase in anti-inflammatory factors and a strong suppression of the pro-inflammatory interleukin 12 (IL-12). In conclusion, the anti-inflammatory environment in muscle that is promoted by the PGC-1 s might contribute to the beneficial effects of these coactivators on muscle function and provides a molecular link underlying the tight mutual regulation of metabolism and inflammation. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:692 / 697
页数:6
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