Department of Biomedical Engineering, University of Alabama at Birmingham, Birmingham, Alabama, 35294, United States.
Department of Medicine and Division of Cardiovascular Disease, University of Alabama at Birmingham, Birmingham, Alabama, 35233, United States.
ACS Appl Mater Interfaces. 2022 Nov 23;14(46):51728-51743. doi: 10.1021/acsami.2c15554. Epub 2022 Nov 8.
Cardiovascular stent technologies have significantly improved over time. However, their optimal performance remains limited by restenosis, thrombosis, inflammation, and delayed re-endothelialization. Current stent designs primarily target inhibition of neointimal proliferation but do not promote functional arterial healing (pro-healing) in order to restore normal vascular reactivity. The endothelial lining that does develop with current stents appears to have loose intracellular junctions. We have developed a pro-healing nanomatrix coating for stents that enhances healing while limiting neointimal proliferation. This builds on our prior work evaluating the effects of the pro-healing nanomatrix coating on cultures of vascular endothelial cells (ECs), smooth muscle cells (SMCs), monocytes, and platelets. However, when a stent is deployed in an artery, multiple vascular cell types interact, and their interactions affect stent performance. Thus, in our current study, an vascular double-layer (VDL) system was used to observe stent effects on communication between different vascular cell types. Additionally, we assessed the pro-healing ability and vascular cell interactions after stent deployment in the VDL system and in a rabbit model, evaluating the nanomatrix-coated stent compared to a commercial bare metal stent (BMS) and a drug eluting stent (DES). results indicated that, in a layered vascular structure, the pro-healing nanomatrix-coated stent could (1) improve endothelialization and endothelial functions, (2) regulate SMC phenotype to reduce SMC proliferation and migration, (3) suppress inflammation through a multifactorial manner, and (4) reduce foam cell formation, extracellular matrix remodeling, and calcification. Consistent with this, results demonstrated that, compared with commercial BMS and DES, this pro-healing nanomatrix-coated stent enhanced re-endothelialization with negligible restenosis, inflammation, or thrombosis. Thus, these findings indicate the unique pro-healing features of this nanomatrix stent coating with superior efficacy over commercial BMS and DES.
心血管支架技术随着时间的推移有了显著的改进。然而,它们的最佳性能仍然受到再狭窄、血栓形成、炎症和内皮延迟再形成的限制。目前的支架设计主要针对抑制新生内膜增殖,但不促进功能性动脉愈合(促进愈合)以恢复正常的血管反应性。目前支架形成的内皮衬里似乎具有松散的细胞内连接。我们开发了一种促进愈合的纳米基质支架涂层,它可以促进愈合,同时限制新生内膜增殖。这是基于我们之前评估促进愈合的纳米基质涂层对血管内皮细胞(ECs)、平滑肌细胞(SMCs)、单核细胞和血小板培养物的影响的工作。然而,当支架在动脉中部署时,多种血管细胞类型相互作用,它们的相互作用会影响支架的性能。因此,在我们目前的研究中,使用血管双层(VDL)系统来观察支架对不同血管细胞类型之间相互作用的影响。此外,我们还在 VDL 系统和兔模型中评估了支架部署后的促进愈合能力和血管细胞相互作用,评估了纳米基质涂层支架与商业裸金属支架(BMS)和药物洗脱支架(DES)的比较。结果表明,在分层血管结构中,促进愈合的纳米基质涂层支架可以(1)改善内皮化和内皮功能,(2)调节平滑肌细胞表型以减少平滑肌细胞增殖和迁移,(3)通过多因素方式抑制炎症,(4)减少泡沫细胞形成、细胞外基质重塑和钙化。与此一致的是,结果表明,与商业 BMS 和 DES 相比,这种促进愈合的纳米基质涂层支架增强了再内皮化,再狭窄、炎症或血栓形成可忽略不计。因此,这些发现表明这种纳米基质支架涂层具有独特的促进愈合特性,其疗效优于商业 BMS 和 DES。