Institute for Biomechanics, ETH Zurich, Zurich, Switzerland.
Institute for Biomechanics, ETH Zurich, Zurich, Switzerland; AO Research Institute Davos, Davos Platz, Switzerland.
Ageing Res Rev. 2024 Jan;93:102118. doi: 10.1016/j.arr.2023.102118. Epub 2023 Nov 5.
Musculoskeletal aging encompasses the decline in bone and muscle function, leading to conditions such as frailty, osteoporosis, and sarcopenia. Unraveling the underlying molecular mechanisms and developing effective treatments are crucial for improving the quality of life for those affected. In this context, accelerated aging models offer valuable insights into these conditions by displaying the hallmarks of human aging. Herein, this review focuses on relevant mouse models of musculoskeletal aging with particular emphasis on frailty, osteoporosis, and sarcopenia. Among the discussed models, PolgA mice in particular exhibit hallmarks of musculoskeletal aging, presenting early-onset frailty, as well as reduced bone and muscle mass that closely resemble human musculoskeletal aging. Ultimately, findings from these models hold promise for advancing interventions targeted at age-related musculoskeletal disorders, effectively addressing the challenges posed by musculoskeletal aging and associated conditions in humans.
肌肉骨骼衰老包括骨骼和肌肉功能的下降,导致脆弱、骨质疏松症和肌肉减少症等疾病。揭示潜在的分子机制并开发有效的治疗方法对于改善受影响人群的生活质量至关重要。在这种情况下,加速衰老模型通过显示人类衰老的特征,为这些疾病提供了有价值的见解。在此,本综述重点介绍了与肌肉骨骼衰老相关的特定小鼠模型,特别是脆弱、骨质疏松症和肌肉减少症。在所讨论的模型中,PolgA 小鼠特别表现出肌肉骨骼衰老的特征,表现为早发性脆弱,以及与人类肌肉骨骼衰老非常相似的减少的骨骼和肌肉质量。最终,这些模型的研究结果有望促进针对与年龄相关的肌肉骨骼疾病的干预措施,有效地应对人类肌肉骨骼衰老和相关疾病带来的挑战。