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用于血管应用的脱细胞基质的生物活性抗血栓修饰

Bioactive Anti-Thrombotic Modification of Decellularized Matrix for Vascular Applications.

作者信息

Glynn Jeremy J, Hinds Monica T

机构信息

Department of Biomedical Engineering, Oregon Health & Science University, Mail Code: CH13B 3303 SW Bond Ave, Portland, OR, 97239, USA.

出版信息

Adv Healthc Mater. 2016 Jun;5(12):1439-46. doi: 10.1002/adhm.201600020. Epub 2016 Apr 13.

DOI:10.1002/adhm.201600020
PMID:27072858
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5753589/
Abstract

The decellularized matrix derived from porcine small intestinal submucosa (SIS) is a widely used biomaterial being investigated for numerous applications. Currently, thrombus deposition and neointimal hyperplasia have limited the use of SIS in some vascular applications. To limit these detrimental processes, this work applies bioactive, endothelial-inspired properties to the material. SIS is modified with the endothelial cell membrane protein thrombomodulin and the glycosaminoglycan heparin to facilitate protein C activation and anticoagulant activity, respectively. Modifying SIS with thrombomodulin alone enables robust activated protein C (APC) generation, and thrombomodulin activity is maintained after prolonged exposure to fluid shear and blood plasma. Heparin-modified SIS has a potent anticoagulant activity. When both modifications are applied sequentially, SIS modified first with thrombomodulin then with heparin retains the full activity of each individual modification. Tubular SIS devices are connected to a baboon arteriovenous shunt to quantify thrombus deposition on these materials. After being exposed to flowing whole blood for 60 min, SIS devices modified first with thrombomodulin then with heparin have significantly less platelet accumulation compared to unmodified SIS devices. These studies demonstrate that modifying SIS with thrombomodulin and heparin confers APC generation and anticoagulant activity that results in reduced thrombogenesis.

摘要

源自猪小肠黏膜下层(SIS)的脱细胞基质是一种广泛应用的生物材料,正在被研究用于众多领域。目前,血栓沉积和新生内膜增生限制了SIS在某些血管应用中的使用。为了限制这些有害过程,本研究将具有生物活性的、受内皮细胞启发的特性应用于该材料。分别用内皮细胞膜蛋白血栓调节蛋白和糖胺聚糖肝素对SIS进行修饰,以促进蛋白C的活化和抗凝活性。单独用血栓调节蛋白修饰SIS能够产生大量活化蛋白C(APC),并且在长时间暴露于流体剪切力和血浆后,血栓调节蛋白的活性得以维持。肝素修饰的SIS具有强大的抗凝活性。当依次进行这两种修饰时,先经血栓调节蛋白修饰再经肝素修饰的SIS保留了每种单独修饰的全部活性。将管状SIS装置连接到狒狒动静脉分流处,以量化这些材料上的血栓沉积情况。在暴露于全血流动60分钟后,与未修饰的SIS装置相比,先经血栓调节蛋白修饰再经肝素修饰的SIS装置的血小板积聚明显减少。这些研究表明,用血栓调节蛋白和肝素修饰SIS可赋予其APC生成和抗凝活性,从而减少血栓形成。

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