Tang Jiandong, Wang Xiangyu, Lin Xu, Wu Chao
Orthopaedics Center, Zigong Fourth People's Hospital, Tan mu lin Street 19#, Zigong, 643099, Sichuan Province, China.
Cell Death Discov. 2024 May 2;10(1):212. doi: 10.1038/s41420-024-01973-w.
The escalating threat of bone-related diseases poses a significant challenge to human health. Mesenchymal stem cell (MSC)-derived extracellular vesicles (MSC-EVs), as inherent cell-secreted natural products, have emerged as promising treatments for bone-related diseases. Leveraging outstanding features such as high biocompatibility, low immunogenicity, superior biological barrier penetration, and extended circulating half-life, MSC-EVs serve as potent carriers for microRNAs (miRNAs), long no-code RNAs (lncRNAs), and other biomolecules. These cargo molecules play pivotal roles in orchestrating bone metabolism and vascularity through diverse mechanisms, thereby contributing to the amelioration of bone diseases. Additionally, engineering modifications enhance the bone-targeting ability of MSC-EVs, mitigating systemic side effects and bolstering their clinical translational potential. This review comprehensively explores the mechanisms through which MSC-EVs regulate bone-related disease progression. It delves into the therapeutic potential of MSC-EVs as adept drug carriers, augmented by engineered modification strategies tailored for osteoarthritis (OA), rheumatoid arthritis (RA), osteoporosis, and osteosarcoma. In conclusion, the exceptional promise exhibited by MSC-EVs positions them as an excellent solution with considerable translational applications in clinical orthopedics.
骨相关疾病不断升级的威胁对人类健康构成了重大挑战。间充质干细胞(MSC)衍生的细胞外囊泡(MSC-EV)作为细胞分泌的天然产物,已成为骨相关疾病的有前景的治疗方法。凭借高生物相容性、低免疫原性、卓越的生物屏障穿透性和延长的循环半衰期等突出特性,MSC-EV作为微小RNA(miRNA)、长链非编码RNA(lncRNA)和其他生物分子的有效载体。这些货物分子通过多种机制在协调骨代谢和血管生成中发挥关键作用,从而有助于改善骨疾病。此外,工程修饰增强了MSC-EV的骨靶向能力,减轻全身副作用并增强其临床转化潜力。本综述全面探讨了MSC-EV调节骨相关疾病进展的机制。它深入研究了MSC-EV作为熟练药物载体的治疗潜力,并通过针对骨关节炎(OA)、类风湿性关节炎(RA)、骨质疏松症和骨肉瘤的工程修饰策略得到增强。总之,MSC-EV展现出的非凡前景使其成为临床骨科中具有相当大转化应用价值的优秀解决方案。