An antioxidant, injectable hydrogel with mitochondrial fusion effect promotes inflamed dental pulp repair via immunomodulation and reactive oxygen species scavenging

活性氧 化学 生物相容性 牙髓干细胞 抗氧化剂 炎症 巨噬细胞极化 氧化应激 牙髓(牙) 细胞生物学 线粒体 线粒体ROS 生物化学 自愈水凝胶 促炎细胞因子 壳聚糖 材料科学 伤口愈合 肝保护 药理学
作者
Dan Wang,Yongle Lv,Fei Xie,Yanqiang Zhao,Bowen Ren,Shanshan Jin,Ningxin Zhu,Man Qin,Zhiqiang Lin,Lei Wang,Yuanyuan Wang
出处
期刊:Biomaterials [Elsevier BV]
卷期号:329: 123985-123985 被引量:2
标识
DOI:10.1016/j.biomaterials.2026.123985
摘要

Vital dental pulp is crucial for the self-repair and long-term retention of teeth with pulpitis; pulp capping materials used for vital pulp therapy must involve controlling inflammatory cascade and regulating inflammatory microenvironment at the same time. Here, we designed a dual-effect hydrogel with immunoregulatory and antioxidant properties to achieve inflamed pulp tissue repair. MASM7, a “mitochondrial glue” promoting mitochondrial fusion, could modulate THP-1-derived macrophages (THP-1-M) polarization to the M2 type under LPS-stimulated inflammatory conditions. Seahorse assay and metabolic-flux analysis (MFA) revealed that mitochondrial fusion modulated metabolic reprogramming of THP-1-M under inflammation from glycolysis to OXPHOS. Moreover, MASM7-treated THP-1-M cells enhanced the repair ability of DPSCs under inflammatory conditions. To realize the application of MASM7 and antioxidant property, chitosan (CS) and methacrylic anhydride (MA) were used to synthesize a methacrylated CS (CSMA) hydrogel, which was then modified with gallic acid (GA) to form a CSMAGA hydrogel. We next confirmed the biocompatibility of this hydrogel. The CSMAGA hydrogel also demonstrated antioxidant properties by scavenging reactive oxygen species. We then confirmed the dual effects of MASM7@CSMAGA hydrogel in rats with LPS-stimulated pulpitis. In conclusion, MASM7@CSMAGA hydrogel can promote pulp tissue repair under inflammatory conditions by modulating macrophage polarization and oxidative stress. • MASM7 promotes mitochondrial fusion and M2 polarization under inflammation. • •MASM7 shifts macrophage metabolism from glycolysis to oxidative phosphorylation. • •MASM7-treated macrophages enhance reparative function of DPSCs in vitro. • •CSMAGA hydrogel is injectable, biocompatible and shows antioxidant properties. • •MASM7@CSMAGA hydrogel promotes inflamed pulp repair in a rat pulpitis model.
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