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首页> 外文期刊>Colloids and Surfaces, B. Biointerfaces >Assessment of cartilage regeneration on 3D collagen-polycaprolactone scaffolds: Evaluation of growth media in static and in perfusion bioreactor dynamic culture
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Assessment of cartilage regeneration on 3D collagen-polycaprolactone scaffolds: Evaluation of growth media in static and in perfusion bioreactor dynamic culture

机译:评估3D胶原蛋白 - 聚己内酯支架上的软骨再生:静态和灌注生物反应器的生长培养基评价

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Efforts on bioengineering are directed towards the construction of biocompatible scaffolds and the determination of the most favorable microenvironment, which will better support cell proliferation and differentiation. Perfusion bioreactors are attracting growing attention as an effective, modern tool in tissue engineering. A natural biomaterial extensively used in regenerative medicine with outstanding biocompatibility, biodegradability and non-toxic characteristics, is collagen, a structural protein with undisputed beneficial characteristics. This is a study designed according to the above considerations. 3D printed polycaprolactone (PCL) scaffolds with rectangular pores were coated with collagen either as a coating on the scaffold's trabeculae, or as a gel-cell solution penetrating scaffolds' pores. We employed histological, molecular and imaging techniques to analyze colonization, proliferation and chondrogenic differentiation of Adipose Derived Mesenchymal Stem Cells (ADMSCs). Two different differentiation culture media were employed to test chondrogenic differentiation on gelated and non gelated PCL scaffolds in static and in perfusion bioreactors dynamic culture conditions. In dynamic culture, non gelated scaffolds combined with our in house TGF-beta(2) based medium, augmented chondrogenic differentiation performance, which overall was significantly less favorable compared to StemPro (TM) propriety medium. The beneficial mechanical stimulus of dynamic culture, appears to outgrow the disadvantage of the "weaker" TGF-beta(2) medium used for chondrogenic differentiation. Even though cells in static culture grew well on the scaffold, there was limited penetration inside the construct, so the purpose of the 3D culture was not fully served. In contrast dynamic culture achieved better penetration and uniform distribution of the cells within the scaffold.
机译:生物工程上的努力是针对生物相容性支架的构建和最有利的微环境的测定,这将更好地支持细胞增殖和分化。灌注生物反应器在组织工程中吸引了越来越多的现代工具。一种具有卓越的生物相容性,生物降解性和无毒特性的再生医学中的一种天然生物材料,是胶原蛋白,一种具有无可争议的有益特征的结构蛋白质。这是根据上述考虑设计的一项研究。 3D印刷的聚己内酯(PCL)带有矩形孔的支架用胶原蛋白涂覆作为支架的小梁的涂层,或作为穿透支架孔的凝胶细胞溶液。我们使用组织学,分子和成像技术来分析脂肪衍生的间充质干细胞(ACMSCs)的殖民化,增殖和软骨形成分化。使用两种不同的分化培养基在静态和灌注生物反应器中测试凝胶化和非凝胶化PCL支架上的软骨形成分化。在动态培养方面,非凝胶化支架与我们在House TGF-β(2)的培养基结合,增强软弱化分化性能,与Syppro(TM)适当介质相比,总体上显着不利。动态培养的有益机械刺激似乎长度过度用于软骨分化的“弱”TGF-β(2)培养基的缺点。尽管静态文化中的细胞在脚手架上生长得很好,但构造内部有限的渗透,因此3D培养的目的没有完全服务。相比之下,动态培养达到了脚手架内细胞的更好的渗透和均匀分布。

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