骨关节炎
医学
软骨
病理
髁突
微泡
颞下颌关节
化学
外科
解剖
小RNA
生物化学
替代医学
基因
作者
Jianping Zhou,Si‐Si Peng,Jie Xu,Xingwang Cheng,X.D. Wang,Jiachun Tao,Hongwei Dai,Xin Cao
标识
DOI:10.1096/fj.202400448rr
摘要
Abstract Temporomandibular joint osteoarthritis (TMJOA) is a degenerative ailment that causes slow cartilage degeneration, aberrant bone remodeling, and persistent discomfort, leading to a considerable reduction in the patient's life quality. Current treatment options for TMJOA have limited efficacy. This investigation aimed to explore a potential strategy for halting or reversing the progression of TMJOA through the utilization of exosomes (EXOs) derived from urine‐derived stem cells (USCs). The USC‐EXOs were obtained through microfiltration and ultrafiltration techniques, followed by their characterization using particle size analysis, electron microscopy, and immunoblotting. Subsequently, an in vivo model of TMJOA induced by mechanical force was established. To assess the changes in the cartilage of TMJOA treated with USC‐EXOs, we performed histology analysis using hematoxylin–eosin staining, immunohistochemistry, and histological scoring. Our findings indicate that the utilization of USC‐EXOs yields substantial reductions in TMJOA, while concurrently enhancing the structural integrity and smoothness of the compromised condylar cartilage surface. Additionally, USC‐EXOs exhibit inhibitory effects on osteoclastogenic activity within the subchondral bone layer of the condylar cartilage, as well as attenuated apoptosis in the rat TMJ in response to mechanical injury. In conclusion, USC‐EXOs hold considerable promise as a potential therapeutic intervention for TMJOA.
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