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基质金属蛋白酶响应性基因递释表面增强原位内皮化。

Matrix-Metalloproteinase-Responsive Gene Delivery Surface for Enhanced in Situ Endothelialization.

机构信息

School of Chemical Engineering and Technology, Tianjin University, Yaguan Road 135, Tianjin 300350, China.

Collaborative Innovation Center of Chemical Science and Chemical Engineering (Tianjin), Tianjin 300350, China.

出版信息

ACS Appl Mater Interfaces. 2020 Sep 9;12(36):40121-40132. doi: 10.1021/acsami.0c11971. Epub 2020 Aug 25.

Abstract

Although blood-contacting medical devices have been widely used in the biomedical field, their low endothelialization seriously limits their treatment success. Gene transfection can enhance the proliferation and migration of endothelial cells (ECs) in culture, yet using this technology to realize surface endothelialization still faces great challenges. Herein, we developed a matrix metalloproteinase (MMP) responsive gene delivery surface for in situ smart release of genes from the biomaterial surface upon EC attachment and adhesion. The released genes induced by ECs can, in turn, effectively transfect ECs and enhance the surface endothelialization. An MMP-responsive gene delivery surface (Au-MCP@NPs) was constructed by immobilizing gene complex nanoparticles (NPs) onto a Au surface with MMP-cleavable peptide (MCP) grafted via biotin-avidin interaction. The Au-MCP@NP surface was demonstrated to responsively release NPs under the action of MMPs. More importantly, ECs were effectively transfected on this surface, leading to enhanced proliferation/migration in vitro. The in situ surface endothelialization was evaluated via implanting Au-MCP@NPs into rat aortas. The in vivo results demonstrated that this smart Au-MCP@NP surface could lead to the localized upregulation of ZNF580 protein and accelerate in situ endothelialization. This smart MMP-responsive gene delivery surface provided a promising and powerful strategy for enhanced in situ endothelialization of blood-contacting medical devices.

摘要

虽然血液接触型医疗器械已在生物医学领域得到广泛应用,但它们的低内皮化严重限制了其治疗效果。基因转染可以增强培养中的内皮细胞(ECs)的增殖和迁移,然而,使用这种技术来实现表面内皮化仍然面临巨大挑战。在这里,我们开发了一种基质金属蛋白酶(MMP)响应性基因传递表面,用于在 EC 附着和黏附时从生物材料表面原位智能释放基因。EC 诱导的释放基因可以反过来有效转染 ECs 并增强表面内皮化。通过将基因复合物纳米颗粒(NPs)固定到通过生物素-亲和素相互作用接枝 MMP 可切割肽(MCP)的 Au 表面上,构建了 MMP 响应性基因传递表面(Au-MCP@NPs)。Au-MCP@NP 表面在 MMP 的作用下被证明可以响应性地释放 NPs。更重要的是,ECs 在该表面上得到了有效的转染,导致体外增殖/迁移增强。通过将 Au-MCP@NPs 植入大鼠主动脉来评估原位表面内皮化。体内结果表明,这种智能 Au-MCP@NP 表面可以导致局部上调 ZNF580 蛋白并加速原位内皮化。这种智能 MMP 响应性基因传递表面为增强血液接触型医疗器械的原位内皮化提供了一种有前途和强大的策略。

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