旋转生物反应器中骨细胞外基质的形成:人间充质基质细胞在薄聚合物支架上的预播种

Q3 Biochemistry, Genetics and Molecular Biology
P. M. Larionov, N. A. Maslov, Vladimir Leonidovitch Ganymedov, V. Tereshchenko, A. Samokhin, E. Tsibulskaya
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引用次数: 0

摘要

背景:已知假体周围骨溶解是关节置换术或牙种植后无菌性不稳定的主要原因。使用流动或旋转生物反应器生产的组织工程支架,允许骨形成区域,似乎是治疗此类骨病变的一种有前途的方法。目的:评估在同轴旋转生物反应器中培养支架三周内的骨新细胞外基质形成,产生初步的数学模型FSS值,旨在开发用于预防假体周围骨溶解的组织工程支架,但反应器的关键特性如流体剪切应力(FSS)应进行微调,以获得良好的细胞密度并防止支架细胞损失。方法:采用静电纺丝法制备薄膜可生物降解聚合物载体,然后与人间充质基质细胞(hMSCs)一起在旋转生物反应器中培养3周,得到初步数学模型计算的FSS为4 ~ 8 mPa。结果用激光扫描共聚焦显微镜免疫荧光和电子扫描显微镜光谱学进行评估。结果:培养2周后,静态条件下培养的hMSC细胞密度与生物反应器培养的hMSC细胞密度无显著差异,但3周后,生物反应器中的细胞密度比静态条件下增加了35%(高达3.53×106±462 / 1 cm2, P < 0.001)。I型胶原在生物反应器中培养2周和3周后的免疫荧光强度分别提高了2.5倍(48.3±0.39 a.u, P < 0.001)和1.31倍(74.0±0.29 a.u, P < 0.001),而骨桥蛋白在静态条件下培养3周后的免疫荧光强度与生物反应器中相似。结论:利用数学模拟的FSS值对反应器特性进行优化,可在旋转生物反应器中3周内显著提高细胞的增殖、分化,并促进新细胞外基质的形成。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Formation of bone extracellular matrix in a rotational bioreactor: Preseeding of human mesenchymal stromal cells on a thin polymer scaffold
BACKGROUND: Periprosthetic osteolysis is known to be the main reason for aseptic instability after the arthroplasty or dental implantation. The use of tissue-engineered scaffolds that allow bone formation area, produced using flow or rotational bioreactor, seems to be a promising approach for such bone lesions treatment. OBJECTIVE: To evaluate the bone neo-extracellular matrix formation within the three-week culture of a scaffold in a coaxial rotational bioreactor generating the preliminary mathematically modelled FSS values with the aim to develop a tissue-engineered scaffold for periprosthetic osteolysis prevention, but reactor critical characteristics like fluid shear stress (FSS) should be fine-tuned to achieve good cell density and prevent cell loss by the scaffold. METHODS: Thin film biodegradable polymer carrier, produced with electrospun and then seeded with hMSCs (human mesenchymal stromal cell) and culture for three weeks in rotational bioreactor, which generates the preliminary math model-calculated FSS from 4 to 8 mPa. Results were assessed with laser scanning confocal microscopy with immunofluorescence, and electron scanning microscopy with spectroscopy. RESULTS: After two weeks of culture, there were no significant differences between the density of hMSC cultured in the static conditions and bioreactor but after 3 weeks the cell density in the bioreactor increased by 35% compared to the static conditions (up to 3.53×106±462 per 1 cm2, P < 0.001). The immunofluorescence intensity exhibited by type I collagen after two and three weeks of culture increased 2.5-fold (48.3±0.39 a.u., P < 0.001) and 1.31-fold (74.0±0.29 a.u., P < 0.001) in the bioreactor, but for osteopontin after 3 weeks of culture in the static conditions was similar to those in the bioreactor. CONCLUSIONS: Optimization of the reactor characteristics with the mathematically modelled FSS values could significantly improve cell proliferation, differentiation, and enhanced formation of the neo-extracellular matrix within 3 weeks in the rotational bioreactor.
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来源期刊
Journal of Cellular Biotechnology
Journal of Cellular Biotechnology Biochemistry, Genetics and Molecular Biology-Biotechnology
CiteScore
0.70
自引率
0.00%
发文量
13
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