Interventional Strategies to Delay Aging-Related Dysfunctions of the Musculoskeletal System

医学 自噬 骨关节炎 衰老 骨质疏松症 PI3K/AKT/mTOR通路 间充质干细胞 肌萎缩 生物信息学 干细胞 软骨 软骨细胞 再生医学 病理 生物 信号转导 内科学 细胞生物学 解剖 细胞凋亡 替代医学 生物化学
作者
Naomasa Fukase,Ingrid K. Stake,Yoichi Murata,William S. Hambright,Sudheer Ravuri,Marc J. Philippon,Johnny Huard
出处
期刊:IntechOpen eBooks [IntechOpen]
被引量:1
标识
DOI:10.5772/intechopen.97311
摘要

Aging affects bones, cartilage, muscles, and other connective tissue in the musculoskeletal system, leading to numerous age-related pathologies including osteoporosis, osteoarthritis, and sarcopenia. Understanding healthy aging may therefore open new therapeutic targets, thereby leading to the development of novel approaches to prevent several age-related orthopaedic diseases. It is well recognized that aging-related stem cell depletion and dysfunction leads to reduced regenerative capacity in various musculoskeletal tissues. However, more recent evidence suggests that dysregulated autophagy and cellular senescence might be fundamental mechanisms associated with aging-related musculoskeletal decline. The mammalian/mechanical target of Rapamycin (mTOR) is known to be an essential negative regulator of autophagy, and its inhibition has been demonstrated to promote longevity in numerous species. Besides, several reports demonstrate that selective elimination of senescent cells and their cognate Senescence-Associated Secretory Phenotype (SASP) can mitigate musculoskeletal tissue decline. Therefore, senolytic drugs/agents that can specifically target senescent cells, may offer a novel therapeutic strategy to treat a litany of age-related orthopaedic conditions. This chapter focuses on osteoarthritis and osteoporosis, very common debilitating orthopaedic conditions, and reviews current concepts highlighting new therapeutic strategies, including the mTOR inhibitors, senolytic agents, and mesenchymal stem cell (MSC)-based therapies.

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