使用微流体制造方法在微结构上自动图案化人脑内皮细胞:一项体外研究

Saurabh S. Aykar, Lionel J. Ouedraogo, Isaac S. Petersen, Mychal J. Trznadel, Nima Alimoradi, Reza Montazami, Amanda L. Brockman, Nicole N. Hashemi
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引用次数: 0

摘要

血脑屏障(BBB)的屏障功能是由毛细血管周围的单层人脑内皮细胞(HBEC)形成的紧密连接提供的。为了在体外模拟这种屏障功能,复制血脑屏障的中空管状结构及其内表面的HBEC单层至关重要。在这里,我们开发了一种微流体制造技术,以在基于藻酸盐的微结构表面形成HBEC图案。使用定制的微流体装置将HBEC接种在这些中空微纤维的内表面上。对接种的HBEC进行了9次监测 并在维护介质中培养以在藻酸盐中空微纤维的内表面上形成单层。使用我们的微流体技术获得了217个细胞/mm长度的中空微纤维的更高的细胞接种密度。此外,在藻酸盐中空微纤维的内表面上接种细胞获得了约96%的高精度。本研究中说明的微流体方法可以推断为在具有细胞相容性ECM基质蛋白的藻酸盐中空微纤维内表面上获得不同细胞类型的单层。此外,它将使我们能够通过紧密复制天然结构的结构属性,在体外制造一系列微血管系统。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Automated patterning of human brain endothelial cells on microstructures using a microfluidic manufacturing approach: An in vitro study

Barrier functionality of the blood–brain barrier (BBB) is provided by the tight junctions formed by a monolayer of the human brain endothelial cells (HBECs) internally around the blood capillaries. To mimic such barrier functionality in vitro, replicating the hollow tubular structure of the BBB along with the HBECs monolayer on its inner surface is crucial. Here, we developed a microfluidic manufacturing technique to pattern the HBECs on the surface of alginate-based microstructures. The HBECs were seeded on the inner surface of these hollow microfibers using a custom-built microfluidic device. The seeded HBECs were monitored for 9 days after manufacturing and cultured to form a monolayer on the inner surface of the alginate hollow microfibers in the maintenance media. A higher cell seeding density of 217 cells/mm length of the hollow microfiber was obtained using our microfluidic technique. Moreover, high accuracy of around 96% was obtained in seeding cells on the inner surface of alginate hollow microfibers. The microfluidic method illustrated in this study could be extrapolated to obtain a monolayer of different cell types on the inner surface of alginate hollow microfibers with cell-compatible ECM matrix proteins. Furthermore, it will enable us to manufacture a range of microvascular systems in vitro by closely replicating the structural attributes of the native structure.

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