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用于模块化组织工程的互穿藻酸盐-胶原蛋白聚合物网络微球

Interpenetrating Alginate-Collagen Polymer Network Microspheres for Modular Tissue Engineering.

作者信息

Mahou Redouan, Vlahos Alexander E, Shulman Avital, Sefton Michael V

机构信息

Institute of Biomaterials and Biomedical Engineering, University of Toronto, Toronto, Ontario M5S 3G9, Canada.

Department of Chemical Engineering and Applied Chemistry, University of Toronto, Toronto, Ontario M5S 3E5, Canada.

出版信息

ACS Biomater Sci Eng. 2018 Nov 12;4(11):3704-3712. doi: 10.1021/acsbiomaterials.7b00356. Epub 2017 Aug 9.

Abstract

The lack of vascularization limits the creation of engineered tissue constructs with clinically relevant sizes. We pioneered a bottom-up process (modular tissue engineering) in which constructs with intrinsic vasculature were assembled from endothelialized building blocks. In this study, we prepared an interpenetrating polymer network (IPN) hydrogel from a collagen-alginate blend and evaluated its use as microspheres in modular tissue engineering. Ionotropic gelation of alginate was combined with collagen fibrillogenesis, and the resulting hydrogel was stiffer and had greater resistance to enzymatic degradation relative to that of collagen alone; the viability of embedded mesenchymal stromal cells (adMSC) was unaltered. IPN microspheres were fabricated by a coaxial air-flow technique, and an additional step of collagen coating was required to have human umbilical vein endothelial cells (HUVEC) attach and proliferate. When implanted subcutaneously in SCID/bg mice, adMSC-HUVEC microspheres promoted more blood vessels at day 7 relative to microspheres without adMSC but coated with HUVEC. Perfusion studies confirmed that these vessels were connected to the host vasculature. Fewer vessels were detected in both groups at day 21, but in adMSC-HUVEC explants, more smooth muscle cells had wrapped around vessels, and CLARITY processing of whole explants revealed a restricted leakage of blood. The capacity for rapid gelation and high throughput production are promising features for the use of these microspheres in modular tissue engineering.

摘要

血管化的缺乏限制了具有临床相关尺寸的工程组织构建体的创建。我们开创了一种自下而上的方法(模块化组织工程),其中具有内在血管系统的构建体由内皮化的构建模块组装而成。在本研究中,我们由胶原蛋白 - 藻酸盐共混物制备了一种互穿聚合物网络(IPN)水凝胶,并评估了其作为模块化组织工程中的微球的用途。藻酸盐的离子凝胶化与胶原蛋白的原纤维形成相结合,所得水凝胶比单独的胶原蛋白更硬,对酶降解具有更大的抵抗力;包埋的间充质基质细胞(adMSC)的活力未改变。IPN微球通过同轴气流技术制造,并且需要额外的胶原蛋白包被步骤以使人类脐静脉内皮细胞(HUVEC)附着并增殖。当皮下植入SCID/bg小鼠时,与没有adMSC但包被有HUVEC的微球相比,adMSC - HUVEC微球在第7天促进了更多血管的形成。灌注研究证实这些血管与宿主血管系统相连。在第21天,两组中检测到的血管较少,但在adMSC - HUVEC外植体中,更多的平滑肌细胞围绕血管缠绕,并且整个外植体的CLARITY处理显示血液泄漏受限。快速凝胶化和高通量生产的能力是这些微球在模块化组织工程中应用的有前景的特性。

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