Mendelsohn Daniel H, Walter Nike, Cheung Wing-Hoi, Wong Ronald Man Yeung, Schönmehl Rebecca, Winter Lina, El Khassawna Thaqif, Heiss Christian, Brochhausen Christoph, Rupp Markus
Institute of Pathology, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany; Friedrich-Baur-Institute, Department of Neurology, LMU Clinic Munich, Germany.
Department of Psychosomatic Medicine, University Medical Center Regensburg, Regensburg, Germany.
Redox Biol. 2025 Jun;83:103667. doi: 10.1016/j.redox.2025.103667. Epub 2025 May 7.
Mitochondria are essential regulators of bone health, controlling cell differentiation, cellular energy production, immune function, osteogenesis, and osteoclast activity. Their dysfunction is linked to orthopedic disorders such as osteoporosis, osteoarthritis, and osteomyelitis, contributing to impaired bone homeostasis and increased fracture risk. While mitochondrial research has been more advanced in fields such as cardiology and neurology, emerging therapeutic strategies from these areas are beginning to show potential for translation into orthopedics. These include mitochondrial biogenesis stimulation, mitochondrial fission inhibition, antioxidant therapies, mitochondrial transplantation, and photobiomodulation, which have demonstrated success in enhancing tissue repair, reducing oxidative stress, and improving overall cellular function in non-orthopedic applications. The novel inhibitor of mitochondrial fission and accumulation of reactive oxygen species Mdivi-1 offers potential to improve clinical outcomes of bone diseases by alleviating cellular dysfunction and preventing bone loss. While these treatments are still in the developmental phase, they present innovative approaches to address mitochondrial dysfunction in orthopedic conditions, potentially transforming bone disease management and enhancing patient outcomes. This report explores research regarding the involvement of mitochondrial health in bone and joint function and discusses possible future treatment strategies targeting mitochondria in orthopedic conditions.
线粒体是骨骼健康的重要调节因子,控制着细胞分化、细胞能量产生、免疫功能、骨生成和破骨细胞活性。它们的功能障碍与骨质疏松症、骨关节炎和骨髓炎等骨科疾病有关,导致骨稳态受损和骨折风险增加。虽然线粒体研究在心脏病学和神经学等领域更为先进,但这些领域新兴的治疗策略已开始显示出转化应用于骨科的潜力。这些策略包括刺激线粒体生物合成、抑制线粒体分裂、抗氧化疗法、线粒体移植和光生物调节,这些在非骨科应用中已证明在促进组织修复、减少氧化应激和改善整体细胞功能方面取得了成功。线粒体分裂和活性氧积累的新型抑制剂Mdivi-1有望通过减轻细胞功能障碍和预防骨质流失来改善骨疾病的临床结果。虽然这些治疗仍处于开发阶段,但它们为解决骨科疾病中的线粒体功能障碍提供了创新方法,有可能改变骨疾病的管理并改善患者预后。本报告探讨了关于线粒体健康在骨骼和关节功能中的作用的研究,并讨论了未来针对骨科疾病中线粒体的可能治疗策略。