Su Yajuan, Sun Jingyu, Li Xiaobo, Huang Feier, Kong Yunhui, Chen Zian, Zhang Jingzhi, Qin Duran, Chen Xiangyi, Wang Zhaoyue, Pei Yu, Gong Mengting, Yang Kaijiang, Xu Minglu, Dong Yu, He Qing, Zhang Zhen-Ning, Sheng Zhejin, Deng Qiaolin, Wang Hong, Wang Gaowei, Hu Ping, Le Rongrong, Gao Shaorong, Li Weida
Institute for Regenerative Medicine, State Key Laboratory of Cardiology and Medical Innovation Center, Shanghai East Hospital, Frontier Science Center for Stem Cell Research, Shanghai Key Laboratory of Signaling and Disease Research, School of Life Sciences and Technology, Sports and Health Research Center, Tongji University Department of Physical Education, Tongji University, Shanghai 200092, China; Tsingtao Advanced Research Institute, Tongji University, Qingdao 266071, China.
Institute for Regenerative Medicine, State Key Laboratory of Cardiology and Medical Innovation Center, Shanghai East Hospital, Frontier Science Center for Stem Cell Research, Shanghai Key Laboratory of Signaling and Disease Research, School of Life Sciences and Technology, Sports and Health Research Center, Tongji University Department of Physical Education, Tongji University, Shanghai 200092, China.
Cell Rep Med. 2025 May 20;6(5):102089. doi: 10.1016/j.xcrm.2025.102089. Epub 2025 Apr 22.
CD47-blocking antibody is a well-known potential antibody drug for tumor immunotherapy. However, it is unclear whether CD47-blocking antibody can protect against metabolic disorders. We report that high-fat diet (HFD)-induced obesity increases CD47 expression, while exercise downregulates it in skeletal muscle. Administration of CD47-blocking antibody in mice prevents HFD-induced weight gain and glucose intolerance, enhances exercise capacity, and improves body composition and skeletal muscle mitochondrial function. Mechanistically, the protective effects conferred by CD47-blocking antibody are mediated through activation of AMP-activated protein kinase (AMPK) in skeletal muscle. Consistently, muscle-specific CD47-knockout mice show similar metabolic improvements, indicating a direct muscle-specific role of CD47 in regulating AMPK activation in vivo. Furthermore, the CD47-blocking antibody reduces the phosphorylation of heat shock protein 90α (HSP90α) to activate AMPK in skeletal muscle. In conclusion, CD47-blocking antibody confers metabolic benefits by activating the AMPK pathway in skeletal muscle.
CD47阻断抗体是一种众所周知的用于肿瘤免疫治疗的潜在抗体药物。然而,目前尚不清楚CD47阻断抗体是否能预防代谢紊乱。我们报告称,高脂饮食(HFD)诱导的肥胖会增加CD47的表达,而运动则会下调骨骼肌中的CD47表达。给小鼠注射CD47阻断抗体可预防HFD诱导的体重增加和葡萄糖不耐受,增强运动能力,并改善身体组成和骨骼肌线粒体功能。从机制上讲,CD47阻断抗体的保护作用是通过激活骨骼肌中的AMP激活蛋白激酶(AMPK)介导的。一致的是,肌肉特异性CD47基因敲除小鼠表现出类似的代谢改善,表明CD47在体内调节AMPK激活中具有直接的肌肉特异性作用。此外,CD47阻断抗体可降低热休克蛋白90α(HSP90α)的磷酸化,从而激活骨骼肌中的AMPK。总之,CD47阻断抗体通过激活骨骼肌中的AMPK途径带来代谢益处。