| Autor: |
Dai, Bingyang, Zhu, Yuwei, Li, Xu, Liang, Zuru, Xu, Shunxiang, Zhang, Shian, Zhang, Zhe, Bai, Shanshan, Tong, Wenxue, Cao, Mingde, Li, Ye, Zhu, Xiaobo, Liu, Wei, Zhang, Yuantao, Chang, Liang, Yung, Patrick Shu‐hang, Ki‐wai Ho, Kevin, Xu, Jiankun, Ngai, To, Qin, Ling |
| Předmět: |
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| Zdroj: |
Advanced Science; 8/4/2023, Vol. 10 Issue 22, p1-18, 18p |
| Abstrakt: |
The knowledge of osteoarthritis (OA) has nowadays been extended from a focalized cartilage disorder to a multifactorial disease. Although recent investigations have reported that infrapatellar fat pad (IPFP) can trigger inflammation in the knee joint, the mechanisms behind the role of IPFP on knee OA progression remain to be defined. Here, dysregulated osteopontin (OPN) and integrin β3 signaling are found in the OA specimens of both human and mice. It is further demonstrated that IPFP‐derived OPN participates in OA progression, including activated matrix metallopeptidase 9 in chondrocyte hypertrophy and integrin β3 in IPFP fibrosis. Motivated by these findings, an injectable nanogel is fabricated to provide sustained release of siRNA Cd61 (RGD−Nanogel/siRNA Cd61) that targets integrins. The RGD−Nanogel possesses excellent biocompatibility and desired targeting abilities both in vitro and in vivo. Local injection of RGD−Nanogel/siRNA Cd61 robustly alleviates the cartilage degeneration, suppresses the advancement of tidemark, and reduces the subchondral trabecular bone mass in OA mice. Taken together, this study provides an avenue for developing RGD−Nanogel/siRNA Cd61 therapy to mitigate OA progression via blocking OPN‐integrin β3 signaling in IPFP. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
| Externí odkaz: |
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