材料科学
树枝状大分子
PEG比率
聚酰胺
胺气处理
吸附
骨关节炎
化学工程
高分子化学
有机化学
医学
化学
替代医学
财务
病理
工程类
经济
作者
Yuzhuo Hei,Jingyi Du,Zhizhao Deng,Yifan Deng,Yu Guan,Jing Yang,Sufang Chen,Ziyi Zhang,Siqing Jiang,Qingbin Zhang
标识
DOI:10.1021/acsami.4c08569
摘要
Temporomandibular joint osteoarthritis (TMJ OA) is characterized by the degeneration of cartilage and subchondral bone. In this study, we observed a significant increase in cell-free DNA (cfDNA) levels during the progression of TMJ OA. Bioinformatics analysis identified TLR9 as a pivotal molecule in TMJ OA pathogenesis. The polyamidoamine (PAMAM) dendrimer characterized by a well-structured, highly branched, and reactive nature, exhibits robust binding and clearance capabilities for cfDNA. However, the abundant amino groups on the surface of PAMAM lead to its inherent toxicity. To mitigate this, PEG-5000 was conjugated to the surface of PAMAM dendrimers, enhancing safety. Our results indicate that PEG-PAMAM effectively inhibits the upregulation of the TLR9 protein in TMJ OA, significantly suppressing the activation of the p-IκBα/p-NF-κB signaling pathway and subsequently decreasing chondrocyte inflammation and apoptosis, as evidenced by both in vivo and in vitro experiments. We conclude that PEG-PAMAM is a safe and effective material for in vivo applications, offering a promising therapeutic strategy for TMJ OA by targeting cfDNA clearance.
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