软骨
线粒体
叙述性评论
叙述的
生物
医学
细胞生物学
病理
解剖
重症监护医学
艺术
文学类
作者
Daniel H. Mendelsohn,Nike Walter,Wing‐Hoi Cheung,Ronald Man Yeung Wong,Rebecca Schönmehl,Lina Winter,Thaqif El Khassawna,Christian Heiß,Christoph Brochhausen,Markus Rupp
出处
期刊:Redox biology
[Elsevier BV]
日期:2025-05-08
卷期号:83: 103667-103667
标识
DOI:10.1016/j.redox.2025.103667
摘要
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.
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