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利用猪内皮祖细胞在静电纺丝支架上构建抗血小板黏附层。

Engineering an antiplatelet adhesion layer on an electrospun scaffold using porcine endothelial progenitor cells.

机构信息

Department of Biomedical Engineering, University of Alabama at Birmingham, Birmingham, Alabama, USA.

出版信息

J Biomed Mater Res A. 2011 May;97(2):145-51. doi: 10.1002/jbm.a.33040. Epub 2011 Mar 2.

Abstract

In coronary artery bypass graft interventions, luminal thrombosis is one of the greatest challenges for polymeric grafts with a luminal diameter less than 4 mm. Previously, we reported the fabrication of a highly porous micro/nanofibrous electrospun scaffold and demonstrated the excellent biocompatibility of the scaffolding materials with human endothelial cells. In this study, we explored the engineering of an antithrombotic layer on the scaffold's lumen within 48 h, using peripheral blood-derived porcine endothelial progentior cells (EPC). Flow cytometric results showed that they were CD31(-) but highly CD34(+) and CD105(+) , suggesting the primitive nature of these freshly isolated EPC. The vast majority of EPC readily took up low density lipoprotein, confirming their endothelial phenotype. These EPC also exhibited a strong proliferation capacity on the scaffold for up to 11 days. A confluent layer could be easily engineered within 24 h, which successfully prevented platelet adhesion, a critical step in the cascade of thrombotic events. We concluded that this scaffold could afford a convenient means for the regeneration of a functional cardiovascular endothelium shortly after implantation. © 2011 Wiley Periodicals, Inc. J Biomed Mater Res Part A:, 2011.

摘要

在冠状动脉旁路移植术干预中,对于管腔直径小于 4 毫米的聚合物移植物,管腔内血栓形成是最大的挑战之一。以前,我们报道了一种高度多孔的微/纳米纤维电纺支架的制造,并证明了支架材料与人内皮细胞具有优异的生物相容性。在这项研究中,我们在 48 小时内探索了在支架管腔内工程化抗血栓层,使用外周血衍生的猪内皮前体细胞(EPC)。流式细胞术结果表明,它们是 CD31(-),但高度 CD34(+)和 CD105(+),表明这些新分离的 EPC 具有原始特性。绝大多数 EPC 很容易摄取低密度脂蛋白,证实了它们的内皮表型。这些 EPC 在支架上的增殖能力也很强,最长可达 11 天。在 24 小时内可以很容易地构建出一个密集的层,这成功地阻止了血小板的黏附,而血小板黏附是血栓形成级联反应中的关键步骤。我们得出结论,这种支架可以为植入后短时间内功能性心血管内皮的再生提供一种方便的方法。©2011 Wiley 期刊,Inc. J Biomed Mater Res Part A:,2011 年。

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