Department of Oral and Cranio-maxillofacial Surgery, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine; College of Stomatology, Shanghai Jiao Tong University; National Center for Stomatology; National Clinical Research Center for Oral Diseases; Shanghai Key Laboratory of Stomatology; Shanghai Research Institute of Stomatology; Research Unit of Oral and Maxillofacial Regenerative Medicine, Chinese Academy of Medical Sciences, Shanghai, China.
Obstetrics Department, Shanghai First Maternity and Infant Hospital, School of Medicine, Tongji University, Shanghai, China.
Sci Adv. 2024 Apr 12;10(15):eadl0372. doi: 10.1126/sciadv.adl0372.
Aging skin, vulnerable to age-related defects, is poor in wound repair. Metabolic regulation in accumulated senescent cells (SnCs) with aging is essential for tissue homeostasis, and adequate ATP is important in cell activation for aged tissue repair. Strategies for ATP metabolism intervention hold prospects for therapeutic advances. Here, we found energy metabolic changes in aging skin from patients and mice. Our data show that metformin engineered EV (Met-EV) can enhance aged mouse skin repair, as well as ameliorate cellular senescence and restore cell dysfunctions. Notably, ATP metabolism was remodeled as reduced glycolysis and enhanced OXPHOS after Met-EV treatment. We show Met-EV rescue senescence-induced mitochondria dysfunctions and mitophagy suppressions, indicating the role of Met-EV in remodeling mitochondrial functions via mitophagy for adequate ATP production in aged tissue repair. Our results reveal the mechanism for SnCs rejuvenation by EV and suggest the disturbed energy metabolism, essential in age-related defects, to be a potential therapeutic target for facilitating aged tissue repair.
衰老的皮肤容易出现与年龄相关的缺陷,伤口愈合能力差。衰老过程中积累的衰老细胞 (SnCs) 的代谢调节对于组织稳态至关重要,而充足的 ATP 对于衰老组织修复中的细胞激活也很重要。干预 ATP 代谢的策略有望推动治疗进展。在这里,我们发现了来自患者和小鼠的衰老皮肤中的能量代谢变化。我们的数据表明,二甲双胍工程化的 EV(Met-EV)可以增强老年小鼠皮肤的修复能力,改善细胞衰老并恢复细胞功能障碍。值得注意的是,Met-EV 处理后,糖酵解减少,OXPHOS 增强,导致 ATP 代谢重塑。我们表明 Met-EV 可挽救衰老诱导的线粒体功能障碍和自噬抑制,表明 Met-EV 通过自噬重塑线粒体功能以在衰老组织修复中产生足够的 ATP,从而发挥作用。我们的结果揭示了 EV 使 SnCs 年轻化的机制,并表明与年龄相关缺陷相关的能量代谢紊乱可能是促进衰老组织修复的潜在治疗靶点。