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祝贺韩智慧的论文发表在National Science Review上!
发布时间:2024-06-20

Autocatalytic bifunctional supramolecular hydrogels for osteoporotic bone repair

Schematic illustration of osteogenic enhancement and osteoclastic inhibition by the Ce–Aln gel. The Ce–Aln gel was autocatalysed to enhance the antioxidant capacity in response to ROS in the bone defect environment, cleared ROS to produce oxygen and maintained redox homeostasis in osteoblasts to avoid apoptosis. It inhibited the production of pro-inflammatory macrophages and pro-inflammatory factors to improve the inflammatory microenvironment and promote bone formation, further enhancing the ability of alendronate to inhibit osteoclasts and reverse the in vivo imbalance of bone metabolism (created with BioRender.com).


Abstract:Conventional bone scaffolds, which are mainly composed of highly active osteoclasts and an inflammatory microenvironment with high levels of reactive oxygen species and pro-inflammatory factors, barely satisfy osteoporotic defect repair. Herein, multifunctional self-assembled supramolecular fiber hydrogels (Ce-Aln gel) consisting of alendronate (Aln) and cerium (Ce) ions were constructed for osteoporotic bone defect repair. Based on the reversible interaction and polyvalent cerium ions, the Ce-Aln gel, which was mainly composed of ionic coordination and hydrogen bonds, displayed good injectability and autocatalytic amplification of the antioxidant effect. In vitro studies showed that the Ce-Aln gel effectively maintained the biological function of osteoblasts by regulating redox homeostasis and improved the inflammatory microenvironment to enhance the inhibitory effect on osteoclasts. RNA sequencing further revealed significant down-regulation of various metabolic pathways, including apoptosis signaling, hypoxia metabolism, and TNFa signaling via the NF-κB pathway after treatment with the Ce-Aln gel. In vivo experiments showed that the clinical drug-based Ce-Aln gel effectively promoted the tissue repair of osteoporotic bone defects by improving inflammation and inhibiting osteoclast formation at the defect. Notably, in vivo systemic osteoporosis was significantly ameliorated, highlighting the strong potential of clinical translation for precise therapy of bone defects.


链接https://academic.oup.com/nsr/advance-article/doi/10.1093/nsr/nwae209/7696750?login=true