Targeting ROS in osteoclasts within the OA environment: A novel therapeutic strategy for osteoarthritis management

被引:0
|
作者
Jeon, Seungho [1 ]
Kim, Tae Min [2 ]
Kwon, Gitae [1 ,3 ]
Park, Junyoung [1 ]
Park, Sung Young [2 ,4 ]
Lee, Seoung Hoon [3 ,5 ]
Jin, Eun-Jung [1 ,5 ]
机构
[1] Wonkwang Univ, Dept Biol Sci, Rm 431, Iksan 54538, Jeonbuk, South Korea
[2] Korea Natl Univ Transportat, Dept IT Energy Convergence BK21 FOUR, Chungju, South Korea
[3] Wonkwang Univ, Coll Dent, Dept Oral Microbiol & Immunol, Iksan 54538, Jeonbuk, South Korea
[4] Korea Natl Univ Transportat, Dept Chem & Biol Engn, Chungju 27469, Chungcheongbuk, South Korea
[5] Wonkwang Univ, Integrated Om Inst, Iksan, Jeonbuk, South Korea
来源
基金
新加坡国家研究基金会;
关键词
M-PD hydrogel; osteoarthritis; osteoclast; ROS; joint microenvironment;
D O I
10.1177/20417314241279935
中图分类号
Q813 [细胞工程];
学科分类号
摘要
This study investigated the therapeutic potential of a manganese dioxide-polymer dot (MnO2-PD)-incorporated hydrogel, designated as M-PD hydrogel, for modulating reactive oxygen species (ROS) within the osteoarthritis (OA) environment. Our research highlights the ability of the hydrogel to scavenge ROS, thereby influencing the differentiation of osteoclasts and protecting chondrocytes, offering a novel approach to osteoarthritis (OA) management. Our results indicated that the M-PD hydrogel increased electrical resistance and fluorescence recovery in the presence of osteoclasts, correlating with decreased ROS levels and suppressed expression of osteoclast differentiation markers. Coculture experiments revealed the protective effects of the hydrogel on chondrocytes by reducing the expression of matrix-degrading enzymes. In vivo application in burr holes and/or OA-induced mice revealed a significant reduction in osteoclast formation and cartilage destruction, suggesting the dual therapeutic action of the hydrogel in altering the joint microenvironment. These findings highlight the potential of targeting ROS in osteoclasts as a comprehensive therapeutic approach, offering not only symptomatic relief but also targeting the underlying mechanisms of disease progression in OA.
引用
收藏
页数:15
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