Jones Mitch, Jones Elena, Kouroupis Dimitrios
Department of Chemistry, Loughborough University, Loughborough LE11 3TU, UK.
Leeds Institute of Rheumatic and Musculoskeletal Disease, University of Leeds, Leeds LS2 9JT, UK.
Bioengineering (Basel). 2024 Sep 26;11(10):961. doi: 10.3390/bioengineering11100961.
Osteoarthritis (OA) is a prominent cause of disability, and has severe social and economic ramifications across the globe. The main driver of OA's pervasiveness is the fact that no current medical interventions exist to reverse or even attenuate the degeneration of cartilage within the articular joint. Crucial for cell-to-cell communication, extracellular vesicles (EVs) contribute to OA progression through the delivery of bioactive molecules in the inflammatory microenvironment. By repurposing this acellular means of signal transmission, therapeutic drugs may be administered to degenerated cartilage tissue in the hopes of encouraging regeneration. Positive outcomes are apparent in in vivo studies on this subject; however, for this therapy to prove itself in the clinical world, efforts towards standardizing the characterization, application, biological contents, and dosage are essential.
骨关节炎(OA)是导致残疾的一个主要原因,在全球范围内产生了严重的社会和经济影响。OA普遍存在的主要原因是目前没有任何医学干预措施能够逆转甚至减缓关节内软骨的退化。细胞外囊泡(EVs)对细胞间通讯至关重要,通过在炎症微环境中传递生物活性分子促进OA的进展。通过重新利用这种无细胞信号传递方式,可以将治疗药物施用于退化的软骨组织,以期促进再生。关于这一主题的体内研究有明显的积极结果;然而,要使这种疗法在临床中得到验证,必须努力规范其表征、应用、生物成分和剂量。
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