再生(生物学)
细胞生物学
线粒体
化学
旁分泌信号
炎症
免疫系统
生物物理学
生物
免疫学
生物化学
受体
作者
Xinzhao Jiang,Wei Wang,Jincheng Tang,Meng Han,Yichang Xu,Lichen Zhang,Jie Wu,Yiyang Huang,Zhouye Ding,Huiwen Sun,Kun Xi,Yong Gu,Liang Chen
标识
DOI:10.1002/advs.202306780
摘要
Although mitochondria are crucial for recovery after spinal cord injury (SCI), therapeutic strategies to modulate mitochondrial metabolic energy to coordinate the immune response and nerve regeneration are lacking. Here, a ligand-screened cerium-based metal-organic framework (MOF) with better ROS scavenging and drug-loading abilities is encapsulated with polydopamine after loading creatine to obtain microcapsules (Cr/Ce@PDA nanoparticles), which reverse the energy deficits in both macrophages and neuronal cells by combining ROS scavenging and energy supplementation. It reprogrames inflammatory macrophages to the proregenerative phenotype via the succinate/HIF-1α/IL-1β signaling axis. It also promotes the regeneration and differentiation of neural cells by activating the mTOR pathway and paracrine function of macrophages. In vivo experiments further confirm the effect of the microcapsules in regulating early ROS-inflammation positive-feedback chain reactions and continuously promoting nerve regeneration. This study provides a new strategy for correcting mitochondrial energy deficiency in the immune response and nerve regeneration following SCI.
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