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用于研究凝血生物学的微流控装置。

Microfluidic devices for studying coagulation biology.

机构信息

Wake Forest Institute for Regenerative Medicine, Fetal Research and Therapy Program Wake Forest School of Medicine, Winston-Salem, NC 27157, USA.

Wake Forest Institute for Regenerative Medicine, Fetal Research and Therapy Program Wake Forest School of Medicine, Winston-Salem, NC 27157, USA.

出版信息

Semin Cell Dev Biol. 2021 Apr;112:1-7. doi: 10.1016/j.semcdb.2020.06.002. Epub 2020 Jun 18.

DOI:10.1016/j.semcdb.2020.06.002
PMID:32563678
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7744328/
Abstract

The ability to study the behavior of cells, proteins, and cell-cell or cell-protein interactions under dynamic forces such as shear stress under fluid flow, provides a more accurate understanding of the physiopathology of hemostasis. This review touches upon the traditional methods for studying blood coagulation and platelet aggregation and provides an overview on cellular and protein response to shear stress. We also elaborate on the biological aspects of how cells recognize mechanical forces and convert them into biochemical signals that can drive various signaling pathways. We give a detailed description of the various types of microfluidic devices that are employed to study the complex processes of platelet aggregation and blood coagulation under flow conditions as well as to investigate endothelial shear-response. We also highlight works mimicking artificial vessels as platforms to study the mechanisms of coagulation, and finish our review by describing anticipated clinical uses of microfluidics devices and their standardization.

摘要

在血流剪切力等动态力下研究细胞、蛋白质以及细胞-细胞或细胞-蛋白质相互作用的行为,能够更准确地理解止血的病理生理学。本文回顾了传统的血液凝固和血小板聚集研究方法,并概述了细胞和蛋白质对剪切力的反应。我们还详细阐述了细胞如何识别机械力并将其转化为生化信号,从而驱动各种信号通路的生物学方面。我们详细描述了各种类型的微流控装置,这些装置用于研究流动条件下血小板聚集和血液凝固的复杂过程,以及研究内皮剪切反应。我们还强调了模拟人工血管的工作,将其作为研究凝血机制的平台,并通过描述微流控装置的预期临床用途及其标准化来完成我们的综述。

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Microfluidic devices for studying coagulation biology.用于研究凝血生物学的微流控装置。
Semin Cell Dev Biol. 2021 Apr;112:1-7. doi: 10.1016/j.semcdb.2020.06.002. Epub 2020 Jun 18.
2
Use of microfluidics to assess the platelet-based control of coagulation.使用微流控技术评估基于血小板的凝血控制。
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Microfluidic technology as an emerging clinical tool to evaluate thrombosis and hemostasis.微流控技术作为一种评估血栓形成和止血的新兴临床工具。
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本文引用的文献

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Microvasculature-on-a-chip for the long-term study of endothelial barrier dysfunction and microvascular obstruction in disease.用于疾病中内皮屏障功能障碍和微血管阻塞长期研究的芯片上微血管系统
Nat Biomed Eng. 2018;2:453-463. doi: 10.1038/s41551-018-0224-z. Epub 2018 Apr 23.
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Quantification of Platelet Contractile Movements during Thrombus Formation.血小板在血栓形成过程中的收缩运动定量。
Thromb Haemost. 2018 Sep;118(9):1600-1611. doi: 10.1055/s-0038-1668151. Epub 2018 Aug 15.
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Piezo1 channels are mechanosensors in human fetoplacental endothelial cells.
J Extracell Vesicles. 2023 Dec;12(12):e12368. doi: 10.1002/jev2.12368.
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A Systematic Analysis of Recent Technology Trends of Microfluidic Medical Devices in the United States.美国微流控医疗设备近期技术趋势的系统分析
Micromachines (Basel). 2023 Jun 24;14(7):1293. doi: 10.3390/mi14071293.
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Predicting the In Vivo Performance of Cardiovascular Biomaterials: Current Approaches In Vitro Evaluation of Blood-Biomaterial Interactions.预测心血管生物材料的体内性能:目前的体外血液-生物材料相互作用评估方法。
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Effects of Shear Stress on Production of FVIII and vWF in a Cell-Based Therapeutic for Hemophilia A.剪切应力对基于细胞的甲型血友病治疗中FVIII和vWF产生的影响。
Front Bioeng Biotechnol. 2021 Mar 1;9:639070. doi: 10.3389/fbioe.2021.639070. eCollection 2021.
7
Mesenchymal stromal cell delivery via an ex vivo bioreactor preclinical test system attenuates clot formation for intravascular application.通过体外生物反应器前临床测试系统递送间充质基质细胞可减少血管内应用中的血栓形成。
Stem Cells Transl Med. 2021 Jun;10(6):883-894. doi: 10.1002/sctm.20-0454. Epub 2021 Feb 1.
Piezo1 通道是人类胎盘中皮细胞的机械感受器。
Mol Hum Reprod. 2018 Oct 1;24(10):510-520. doi: 10.1093/molehr/gay033.
4
Endothelial cell culture in microfluidic devices for investigating microvascular processes.用于研究微血管过程的微流控装置中的内皮细胞培养。
Biomicrofluidics. 2018 May 15;12(4):042203. doi: 10.1063/1.5024901. eCollection 2018 Jul.
5
Structure and mechanogating mechanism of the Piezo1 channel.Piezo1 通道的结构和机械门控机制。
Nature. 2018 Feb 22;554(7693):487-492. doi: 10.1038/nature25743. Epub 2018 Jan 22.
6
The physical spacing between the von Willebrand factor D'D3 and A1 domains regulates platelet adhesion in vitro and in vivo.血管性血友病因子 D'D3 结构域与 A1 结构域之间的物理间距调节血小板在体外和体内的黏附。
J Thromb Haemost. 2018 Mar;16(3):571-582. doi: 10.1111/jth.13927. Epub 2018 Jan 22.
7
Margination and stretching of von Willebrand factor in the blood stream enable adhesion.血管中 von Willebrand 因子的边缘和伸展使黏附得以发生。
Sci Rep. 2017 Oct 27;7(1):14278. doi: 10.1038/s41598-017-14346-4.
8
Evaluation of a microfluidic flow assay to screen for von Willebrand disease and low von Willebrand factor levels.评价一种微流控流动分析检测方法,用于筛选血管性血友病和低血管性血友病因子水平。
J Thromb Haemost. 2018 Jan;16(1):104-115. doi: 10.1111/jth.13881. Epub 2017 Nov 23.
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Flow-induced elongation of von Willebrand factor precedes tension-dependent activation.血流诱导的血管性血友病因子伸长先于张力依赖性激活。
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Modeling thrombus formation and growth.模拟血栓形成与生长。
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