微球
细胞生物学
巨噬细胞极化
再生(生物学)
免疫系统
化学
生物物理学
巨噬细胞
生物医学工程
联轴节(管道)
骨愈合
材料科学
炎症
免疫学
作者
Lingjun Wang,Zhengxia Ni,Yiyang Huang,Jiannan Mao,Jie Wu (10038),Wei Wang (17594),Xinzhao Jiang,Liang Zhou,Jincheng Tang,Kun Xi,Yong Gu,Liang Chen
摘要
The skeletal immune microenvironment plays a critical role in the repair of bone defects; however, current strategies focusing on macrophage M2 polarization and their application in bone regeneration remain limited. To address this, we developed a methacrylated gelatin (GelMA) microsphere system using microfluidic technology, co-loading IL-4 and chitosan-BSA nanoparticles (CNP) encapsulating calcitonin gene-related peptide (CGRP) to achieve temporally controlled release and immuno-osteogenic synergistic regulation. In the early stage, IL-4 secretion promotes macrophage polarization toward the M2 phenotype, improving the inflammatory microenvironment, while the sustained release of CGRP subsequently enhances angiogenesis and osteogenic differentiation, establishing a microenvironment favorable for bone regeneration. In a femoral condyle defect model, these composite microspheres significantly accelerated new bone formation and defect healing, exhibiting an osteogenic pattern centered around the microspheres. This study provides a novel temporally controlled release strategy for promoting bone regeneration through immune microenvironment modulation, offering potential translational value in bone tissue engineering.
科研通智能强力驱动
Strongly Powered by AbleSci AI