破骨细胞
化学
再生(生物学)
核化学
生物医学工程
材料科学
化学工程
生物化学
医学
细胞生物学
生物
体外
工程类
作者
Zhengrong Chen,Wen-Xin Yang,Yong Tang,Qianqian Dong,Kui Huang,Jiulin Tan,Jie Zhang,Juan Cai,Qiushan Yu,Qijie Dai,Jianzhong Xu,Shuquan Guo,Ce Dou,Fei Luo
出处
期刊:PubMed
日期:2025-03-26
卷期号:: e2415895-e2415895
标识
DOI:10.1002/advs.202415895
摘要
Osteoporotic bone defects are challenging to repair due to imbalances in bone resorption and formation, coupled with insufficient vascularization. To address these issues, it develops a trifunctional hydrogel (SF-ZIF@NA) designed to selectively inhibit osteoclast activity and enhance vascularized bone regeneration. By enzymatically removing sialic acid, SF-ZIF@NA prevents precursor osteoclasts (pOCs) from fusing into bone-resorbing mature osteoclasts (mOCs), thereby preserving pOCs and their anabolic functions. Additionally, the hydrogel releases Zinc ion (Zn2⁺) in response to acidic conditions, promoting osteogenesis and angiogenesis. In vitro results confirmed that SF-ZIF@NA impedes osteoclast fusion, enhances platelet-derived growth factor-BB (PDGF-BB secretion from pOCs, and activates the FAK (focal adhesion kinase) signaling pathway to stimulate vascularized bone formation. In osteoporotic bone defect models, SF-ZIF@NA accelerated bone repair with increased bone density and vascularization. These findings demonstrate that SF-ZIF@NA offers a targeted and multifunctional strategy for osteoporotic bone regeneration by concurrently modulating osteoclast activity and promoting angiogenesis.
科研通智能强力驱动
Strongly Powered by AbleSci AI