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心血管器械的内皮化。

Endothelialization of cardiovascular devices.

机构信息

Department of Bioengineering, University of Missouri, Columbia, MO 65211, USA.

出版信息

Acta Biomater. 2019 Nov;99:53-71. doi: 10.1016/j.actbio.2019.08.042. Epub 2019 Aug 24.

Abstract

Blood-contacting surfaces of cardiovascular devices are not biocompatible for creating an endothelial layer on them. Numerous research studies have mainly sought to modify these surfaces through physical, chemical and biological means to ease early endothelial cell (EC) adhesion, migration and proliferation, and eventually to build an endothelial layer on the surfaces. The first priority for surface modification is inhibition of protein adsorption that leads to inhibition of platelet adhesion to the device surfaces, which may favor EC adhesion. Surface modification through surface texturing, if applicable, can bring some hopeful outcomes in this regard. Surface modifications through chemical and/or biological means may play a significant role in easy endothelialization of cardiovascular devices and inhibit smooth muscle cell proliferation. Cellular engineering of cells relevant to endothelialization can boost the positive outcomes obtained through surface engineering. This review briefly summarizes recent developments and research in early endothelialization of cardiovascular devices. STATEMENT OF SIGNIFICANCE: Endothelialization of cardiovascular implants, including heart valves, vascular stents and vascular grafts is crucial to solve many problems in our health care system. Numerous research efforts have been made to improve endothelialization on the surfaces of cardiovascular implants, mainly through surface modifications in three ways - physically, chemically and biologically. This review is intended to highlight comprehensive research studies to date on surface modifications aiming for early endothelialization on the blood-contacting surfaces of cardiovascular implants. It also discusses future perspectives to help guide endothelialization strategies and inspire further innovations.

摘要

心血管设备的血液接触表面在创造内皮层方面是不兼容的。许多研究主要试图通过物理、化学和生物学手段来修饰这些表面,以促进早期内皮细胞(EC)的黏附、迁移和增殖,并最终在表面上形成内皮层。表面修饰的首要任务是抑制蛋白质吸附,从而抑制血小板黏附到设备表面,这可能有利于 EC 的黏附。如果适用,通过表面织构化进行的表面修饰在这方面可能会带来一些有希望的结果。通过化学和/或生物学手段进行的表面修饰可能在心血管设备的易于内皮化和抑制平滑肌细胞增殖方面发挥重要作用。与内皮化相关的细胞的细胞工程可以增强通过表面工程获得的积极结果。这篇综述简要总结了心血管设备早期内皮化的最新进展和研究。

意义声明

心血管植入物(包括心脏瓣膜、血管支架和血管移植物)的内皮化对于解决我们医疗保健系统中的许多问题至关重要。已经做出了大量的研究努力来改善心血管植入物表面的内皮化,主要通过三种方式——物理、化学和生物学方式来进行表面修饰。这篇综述旨在强调迄今为止针对心血管植入物血液接触表面早期内皮化的全面研究,讨论未来的展望以帮助指导内皮化策略并激发进一步的创新。

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