多种三维支架与生物反应器刺激对人体细胞反馈联合效应的计算与实验研究

Foteini K. Kozaniti, A. Manara, V. Kostopoulos, P. Mallis, E. Michalopoulos, D. Polyzos, D. Deligianni, D. Portan
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引用次数: 1

摘要

为了研究在生物反应器中动态刺激人类脐带干细胞对3D电纺丝和打印支架的反应,将计算方法与实验装置相结合。使用Comsol软件对与生物反应器工作条件相关的关键参数进行计算研究,以将输出用于计划的实验设置。在理论观察的基础上,分析了进气速度、细胞数、暴露时间等因素对生物反应器的影响,并进行了相应的体外参数调整。将不同数量的MSCs植入3D多孔支架中,并在生物反应器中进行刺激(持续时间0.5和2 h,进口速度3和6 mm/s)。制备了聚己内酯3D电纺丝支架、聚氨酯和聚乳酸3D打印支架并包被纤维连接蛋白。计算研究预测了细胞沉积和附着过程中的初始事件。研究支架内沉积细胞的总蛋白、骨桥蛋白和骨钙素水平;扫描电镜和共聚焦成像证实了生物标志物分析。骨髓间充质干细胞在PCL中增殖良好。聚亚安酯使极快增殖随后分化,而聚亚安酯诱导适度增殖和平行矿化。支架刚度是决定细胞反馈的关键使能参数。
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Computational and Experimental Investigation of the Combined Effect of Various 3D Scaffolds and Bioreactor Stimulation on Human Cells’ Feedback
Computational methods were combined with an experimental setup in order to investigate the response of human umbilical cord stem cells to 3D electrospun and printed scaffolds, when dynamically stimulated in a bioreactor. Key parameters associated to bioreactor working conditions were computationally investigated using Comsol software to use the output for the planned experimental setup. Based on the theoretical observations, the influence of the inlet velocity, cell number, and exposure time in the bioreactor were analyzed and the in vitro parameters were adjusted accordingly. MSCs were seeded in different numbers in the 3D porous scaffolds and stimulated in the bioreactor (0.5 and 2 h duration, 3 and 6 mm/s inlet velocity). Polycaprolactone 3D electrospun, and polyurethane and polylactic acid 3D-printed scaffolds were fabricated and fibronectin-coated. The computational study predicted initial events in the process of cells deposition and attachment. Total protein, osteopontin, and osteocalcin levels in cells deposited in scaffolds were investigated; SEM and confocal imaging confirmed the biomarker analysis. MSCs proliferated well in PCL. Polyurethane enabled extremely rapid proliferation followed by differentiation, while PLA induced a moderate proliferation and parallel mineralization. The scaffolds stiffness has been found as the key enabling parameter decisive for cells feedback.
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