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一种整合了止血主要成分的微工程化血管化出血模型。

A microengineered vascularized bleeding model that integrates the principal components of hemostasis.

作者信息

Sakurai Yumiko, Hardy Elaissa T, Ahn Byungwook, Tran Reginald, Fay Meredith E, Ciciliano Jordan C, Mannino Robert G, Myers David R, Qiu Yongzhi, Carden Marcus A, Baldwin W Hunter, Meeks Shannon L, Gilbert Gary E, Jobe Shawn M, Lam Wilbur A

机构信息

Wallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology and Emory University, 345 Ferst Drive, Atlanta, GA, 30332, USA.

Department of Pediatrics, Divisoin of Pediatric Hematology/Oncology, Aflac Cancer Center and Blood Disorders Center of Children's Healthcare of Atlanta, Emory University School of Medicine, 2015 Uppergate Drive, Atlanta, GA, 30322, USA.

出版信息

Nat Commun. 2018 Feb 6;9(1):509. doi: 10.1038/s41467-018-02990-x.

Abstract

Hemostasis encompasses an ensemble of interactions among platelets, coagulation factors, blood cells, endothelium, and hemodynamic forces, but current assays assess only isolated aspects of this complex process. Accordingly, here we develop a comprehensive in vitro mechanical injury bleeding model comprising an "endothelialized" microfluidic system coupled with a microengineered pneumatic valve that induces a vascular "injury". With perfusion of whole blood, hemostatic plug formation is visualized and "in vitro bleeding time" is measured. We investigate the interaction of different components of hemostasis, gaining insight into several unresolved hematologic issues. Specifically, we visualize and quantitatively demonstrate: the effect of anti-platelet agent on clot contraction and hemostatic plug formation, that von Willebrand factor is essential for hemostasis at high shear, that hemophilia A blood confers unstable hemostatic plug formation and altered fibrin architecture, and the importance of endothelial phosphatidylserine in hemostasis. These results establish the versatility and clinical utility of our microfluidic bleeding model.

摘要

止血过程涉及血小板、凝血因子、血细胞、内皮细胞和血流动力学力之间的一系列相互作用,但目前的检测方法仅评估了这一复杂过程的孤立方面。因此,我们在此开发了一种全面的体外机械损伤出血模型,该模型包括一个“内皮化”微流体系统以及一个可诱导血管“损伤”的微工程气动阀。通过全血灌注,可观察到止血栓的形成并测量“体外出血时间”。我们研究了止血不同组分之间的相互作用,深入了解了几个尚未解决的血液学问题。具体而言,我们可视化并定量证明了:抗血小板药物对凝块收缩和止血栓形成的影响;血管性血友病因子在高剪切力下对止血至关重要;甲型血友病血液导致止血栓形成不稳定且纤维蛋白结构改变;以及内皮磷脂酰丝氨酸在止血中的重要性。这些结果确立了我们微流体出血模型的多功能性和临床实用性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a57/5802762/0b544003f0c0/41467_2018_2990_Fig1_HTML.jpg

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