静电纺丝
巨噬细胞极化
材料科学
血管生成
己内酯
巨噬细胞
M2巨噬细胞
巨噬细胞炎性蛋白
细胞生物学
化学
体外
癌症研究
复合材料
聚合物
聚合
医学
生物
生物化学
作者
Can Cheng,Heng Li,Jingwen Liu,Liang Wu,Zhengdong Fang,Geliang Xu
标识
DOI:10.1021/acsbiomaterials.3c00476
摘要
Tissue engineering approaches such as the electrospinning technique can fabricate nanofibrous scaffolds which are widely used for small-diameter vascular grafting. However, foreign body reaction (FBR) and lack of endothelial coverage are still the main cause of graft failure after the implantation of nanofibrous scaffolds. Macrophage-targeting therapeutic strategies have the potential to address these issues. Here, we fabricate a monocyte chemotactic protein-1 (MCP-1)-loaded coaxial fibrous film with poly(l-lactide-co-ε-caprolactone) (PLCL/MCP-1). The PLCL/MCP-1 fibrous film can polarize macrophages toward anti-inflammatory M2 macrophages through the sustained release of MCP-1. Meanwhile, these specific functional polarization macrophages can mitigate FBR and promote angiogenesis during the remodeling of implanted fibrous films. These studies indicate that MCP-1-loaded PLCL fibers have a higher potential to modulate macrophage polarity, which provides a new strategy for small-diameter vascular graft designing.
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