下调和上调
再生(生物学)
免疫印迹
牙槽
细胞生物学
碱性磷酸酶
间充质干细胞
间质细胞
癌症研究
免疫组织化学
祖细胞
共域化
病理
化学
骨重建
免疫学
骨髓
骨愈合
免疫系统
炎症
生物
NADPH氧化酶
骨吸收
作者
Junyu Liu,Yurou Chen,Xinyao Zhang,Yingge Yue,Yukun Shi,Yuping Ren,Guanhua Lyu,Peiwen Li,Ruxia Hou,Xiangyu Wang
标识
DOI:10.1021/acsami.5c20378
摘要
) at 2 weeks. Critically, immunofluorescence colocalization analysis provided direct spatial evidence that the hydrogel disrupted the pathogenic interaction between IL-17 and phosphorylated STAT3 within the defect microenvironment. By 8 weeks, micro-CT and histology revealed robust bone regeneration, characterized by mature collagen deposition and trabecular reconstruction. Immunohistochemistry confirmed persistent expression of osteogenic proteins (OPG, COL1A1). Major organs showed no pathological changes, confirming systemic biosafety. This glucose-responsive system integrates immunomodulation with osteogenic promotion, offering a promising strategy for diabetic bone repair by addressing the dual challenges of hyperglycemia and IL-17-mediated inflammation, thus presenting a targeted alternative to conventional growth factor-based therapies.
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