Zhu Xiaopeng, Yao Ting, Wang Ru, Guo Shanshan, Wang Xin, Zhou Zhenqi, Zhang Yan, Zhuo Xiaozhen, Wang Ruitao, Li John Zhong, Liu Tiemin, Kong Xingxing
Division of Pediatric Endocrinology Department of Pediatrics UCLA Children's Discovery and Innovation Institute David Geffen School of Medicine at UCLA Los Angeles CA 90095 USA.
Department of Endocrinology and Metabolism Zhongshan Hospital Fudan University Shanghai 200032 P. R. China.
Adv Sci (Weinh). 2020 Aug 1;7(19):2001502. doi: 10.1002/advs.202001502. eCollection 2020 Oct.
Exercise-induced fatigue and exhaustion are interesting areas for many researchers. Muscle glycogen is critical for physical performance. However, how glycogen metabolism is manipulated during exercise is not very clear. The aim here is to assess the impact of interferon regulatory factor 4 (IRF4) on skeletal muscle glycogen and subsequent regulation of exercise capacity. Skeletal muscle-specific IRF4 knockout mice show normal body weight and insulin sensitivity, but better exercise capacity and increased glycogen content with unaltered triglyceride levels compared to control mice on chow diet. In contrast, mice overexpression of IRF4 displays decreased exercise capacity and lower glycogen content. Mechanistically, IRF4 regulates glycogen-associated regulatory subunit protein targeting to glycogen (PTG) to manipulate glucose metabolism in skeletal muscle. Knockdown of PTG can reverse the effects imposed by the absence of IRF4 in vivo. These studies reveal a regulatory pathway including IRF4/PTG/glycogen synthesis on controlling exercise capacity.
运动诱导的疲劳和疲惫是许多研究人员感兴趣的领域。肌肉糖原对身体机能至关重要。然而,运动期间糖原代谢是如何被调控的尚不清楚。本文的目的是评估干扰素调节因子4(IRF4)对骨骼肌糖原的影响以及随后对运动能力的调节。与正常饮食的对照小鼠相比,骨骼肌特异性IRF4基因敲除小鼠体重和胰岛素敏感性正常,但运动能力更强,糖原含量增加,甘油三酯水平未改变。相反,IRF4过表达的小鼠运动能力下降,糖原含量降低。从机制上讲,IRF4通过调节糖原相关调节亚基靶向糖原蛋白(PTG)来调控骨骼肌中的葡萄糖代谢。在体内敲低PTG可逆转因缺乏IRF4所产生的影响。这些研究揭示了一条包括IRF4/PTG/糖原合成在内的控制运动能力的调控途径。