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载单核细胞趋化蛋白-1 的聚(L-丙交酯-己内酯)纤维膜调节巨噬细胞向抗炎表型极化并促进血管生成。

MCP-1-Loaded Poly(l-lactide--caprolactone) Fibrous Films Modulate Macrophage Polarization toward an Anti-inflammatory Phenotype and Improve Angiogenesis.

机构信息

Cheeloo College of Medicine, Shandong University, Jinan, Shandong 250012, P. R. China.

Department of General Surgery, The First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, Anhui 230001, P. R. China.

出版信息

ACS Biomater Sci Eng. 2023 Jul 10;9(7):4356-4367. doi: 10.1021/acsbiomaterials.3c00476. Epub 2023 Jun 27.

Abstract

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--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.

摘要

组织工程方法,如电纺技术,可以制造出广泛用于小直径血管移植的纳米纤维支架。然而,异物反应(FBR)和缺乏内皮细胞覆盖仍然是纳米纤维支架植入后移植失败的主要原因。针对巨噬细胞的治疗策略有可能解决这些问题。在这里,我们制备了一种载有单核细胞趋化蛋白-1(MCP-1)的聚(L-丙交酯-ε-己内酯)(PLCL/MCP-1)同轴纤维膜。PLCL/MCP-1 纤维膜通过持续释放 MCP-1 使巨噬细胞向抗炎 M2 型极化。同时,这些特定功能的极化巨噬细胞可以减轻 FBR 并促进植入纤维膜重塑过程中的血管生成。这些研究表明,载有 MCP-1 的 PLCL 纤维具有更高的调节巨噬细胞极性的潜力,为小直径血管移植设计提供了新的策略。

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