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J R Soc Interface. 2016 Dec;13(125). doi: 10.1098/rsif.2016.0834.
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本文引用的文献

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Human Vascular Microphysiological System for in vitro Drug Screening.用于体外药物筛选的人体血管微生理系统。
Sci Rep. 2016 Feb 18;6:21579. doi: 10.1038/srep21579.
2
Scaffold-free, Human Mesenchymal Stem Cell-Based Tissue Engineered Blood Vessels.无支架、基于人间充质干细胞的组织工程血管
Sci Rep. 2015 Oct 12;5:15116. doi: 10.1038/srep15116.
3
A multilayered microfluidic blood vessel-like structure.一种多层微流控血管样结构。
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4
Hydrogels for Engineering of Perfusable Vascular Networks.用于可灌注血管网络工程的水凝胶
Int J Mol Sci. 2015 Jul 14;16(7):15997-6016. doi: 10.3390/ijms160715997.
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Tunable collagen I hydrogels for engineered physiological tissue micro-environments.用于构建生理性组织微环境的可调谐I型胶原蛋白水凝胶。
PLoS One. 2015 Mar 30;10(3):e0122500. doi: 10.1371/journal.pone.0122500. eCollection 2015.
6
Engineered in vitro disease models.体外构建疾病模型。
Annu Rev Pathol. 2015;10:195-262. doi: 10.1146/annurev-pathol-012414-040418.
7
Microfluidic perfusion culture system for multilayer artery tissue models.用于多层动脉组织模型的微流控灌注培养系统。
Biomicrofluidics. 2014 Dec 3;8(6):064113. doi: 10.1063/1.4903210. eCollection 2014 Nov.
8
Microfluidic organs-on-chips.微流控器官芯片。
Nat Biotechnol. 2014 Aug;32(8):760-72. doi: 10.1038/nbt.2989.
9
Review of collagen I hydrogels for bioengineered tissue microenvironments: characterization of mechanics, structure, and transport.用于生物工程组织微环境的I型胶原蛋白水凝胶综述:力学、结构和传输特性
Tissue Eng Part B Rev. 2014 Dec;20(6):683-96. doi: 10.1089/ten.TEB.2014.0086. Epub 2014 Jul 22.
10
Endothelial repair process and its relevance to longitudinal neointimal tissue patterns: comparing histology with in silico modelling.内皮修复过程及其与纵向新生内膜组织模式的相关性:组织学与计算机模拟比较。
J R Soc Interface. 2014 Mar 12;11(94):20140022. doi: 10.1098/rsif.2014.0022. Print 2014 May 6.

可植入体外动脉:用于血管内装置开发与优化的仪器化平台。

The stentable in vitro artery: an instrumented platform for endovascular device development and optimization.

作者信息

Antoine Elizabeth E, Cornat François P, Barakat Abdul I

机构信息

Hydrodynamics Laboratory (LadHyX), Ecole Polytechnique, Route de Saclay, 91128 Palaiseau, France.

Hydrodynamics Laboratory (LadHyX), Ecole Polytechnique, Route de Saclay, 91128 Palaiseau, France

出版信息

J R Soc Interface. 2016 Dec;13(125). doi: 10.1098/rsif.2016.0834.

DOI:10.1098/rsif.2016.0834
PMID:28003530
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5221533/
Abstract

Although vascular disease is a leading cause of mortality, in vitro tools for controlled, quantitative studies of vascular biological processes in an environment that reflects physiological complexity remain limited. We developed a novel in vitro artery that exhibits a number of unique features distinguishing it from tissue-engineered or organ-on-a-chip constructs, most notably that it allows deployment of endovascular devices including stents, quantitative real-time tracking of cellular responses and detailed measurement of flow velocity and lumenal shear stress using particle image velocimetry. The wall of the stentable in vitro artery consists of an annular collagen hydrogel containing smooth muscle cells (SMCs) and whose lumenal surface is lined with a monolayer of endothelial cells (ECs). The system has in vivo dimensions and physiological flow conditions and allows automated high-resolution live imaging of both SMCs and ECs. To demonstrate proof-of-concept, we imaged and quantified EC wound healing, SMC motility and altered shear stresses on the endothelium after deployment of a coronary stent. The stentable in vitro artery provides a unique platform suited for a broad array of research applications. Wide-scale adoption of this system promises to enhance our understanding of important biological events affecting endovascular device performance and to reduce dependence on animal studies.

摘要

尽管血管疾病是导致死亡的主要原因,但在反映生理复杂性的环境中用于血管生物学过程的可控定量研究的体外工具仍然有限。我们开发了一种新型体外动脉,它具有许多独特特征,使其有别于组织工程或芯片器官构建体,最显著的是它允许部署包括支架在内的血管内装置,能够使用粒子图像测速技术对细胞反应进行定量实时跟踪以及对流速和管腔剪切应力进行详细测量。可植入支架的体外动脉壁由含有平滑肌细胞(SMC)的环形胶原水凝胶组成,其管腔表面衬有单层内皮细胞(EC)。该系统具有体内尺寸和生理流动条件,并允许对SMC和EC进行自动高分辨率实时成像。为了证明概念验证,我们对冠状动脉支架植入后内皮细胞伤口愈合、SMC运动以及内皮上改变的剪切应力进行了成像和量化。可植入支架的体外动脉提供了一个适用于广泛研究应用的独特平台。该系统的广泛采用有望增进我们对影响血管内装置性能的重要生物学事件的理解,并减少对动物研究的依赖。