基于软骨球的无支架方法制备体外关节软骨模型。

Tissue Engineering Part A Pub Date : 2022-01-01 Epub Date: 2021-08-25 DOI:10.1089/ten.TEA.2021.0061
Annachiara Scalzone, Xiao N Wang, Kenny Dalgarno, Ana M Ferreira, Piergiorgio Gentile
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引用次数: 5

摘要

人体关节软骨的体外工程是再生医学的一个挑战。本研究的主要目的是建立一种可重复的无支架软骨细胞球体治疗软骨缺损的体外模型,以便对这类治疗进行系统研究和进一步优化。将人关节软骨细胞(HC)和软骨细胞分化的永生化间充质细胞(Y201-Cs)培养在圆底96孔板上形成多细胞球体,观察其生长动力学,并在培养7 d后评估其活力。然后,按照临床批准的Chondrosphere®(CO.DON AG)技术,将球体组装并在明胶包被的聚(乳酸-羟基乙酸)静电纺丝膜(10个球体/cm2)上培养21天。培养7天后,HC和Y201-C细胞均形成致密且有活力的球体,直径分别从1300±150 μm减小到600±90 μm,从1250±60 μm减小到800±20 μm。根据基因表达和糖胺聚糖定量分析,当球体转移到支撑膜上时,它们粘附在膜上并融合,产生II型胶原蛋白(COL2A1)和聚集蛋白(ACAN)。我们在HC细胞中检测到COL2A1的高表达,而Y201-C构建体的特征是ACAN的表达增加。我们提出的方法允许标准化生产具有可预测几何形状的球体,并使用HC和Y201-C创建可重复的无支架体外ac样结构,显示高表达软骨标志物。此外,可利用的Y201-C电池为球体方法的实验提供了有效的基础模型,以进一步增强该过程。这是基于最近临床批准的软骨球®(CO.DON AG)技术的优化方案开发可重复的无支架体外模型的第一项工作。此外,我们证明了一种可移植的细胞类型(Y201-C)可以产生工程化的软骨样结构,提供了一个可重复的模型,作为在异质细胞群体研究之前进行治疗性治疗实验的关键工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Chondrosphere-Based Scaffold Free Approach to Manufacture an In Vitro Articular Cartilage Model.

In vitro engineering of human articular cartilage (AC) is a regenerative medicine challenge. The main objective of this study was the development of a repeatable scaffold-free in vitro model of chondrocyte spheroid-based treatments of cartilage defects, to allow for systematic study and further optimization of this type of treatment. Human articular chondrocytes (HC) and immortalized mesenchymal cells differentiated in chondrocytes (Y201-Cs) were cultured in round-bottom 96-well plates to produce multicellular spheroids and their growth kinetics, and viability was evaluated over 7 days of culture. Then, the spheroids were assembled and cultured for 21 days on a gelatin-coated poly(lactic-co-glycolic acid) electrospun membrane (10 spheroids/cm2), following a protocol in line with the clinically approved Chondrosphere® (CO.DON AG) technique. Both HC and Y201-C cells formed compact and viable spheroids after 7 days of culture with a reduction of diameter over the 7 days from 1300 ± 150 μm to 600 ± 90 μm and from 1250 ± 60 μm to 800 ± 20 μm for HC and Y201-C, respectively. When the spheroids were transferred onto the support membrane, these adhered on the membrane itself and fused themselves, producing collagen type II (COL2A1) and aggrecan (ACAN), according to gene expression and glycosaminoglycans quantification analyses. We detected higher expression of COL2A1 in HC cells, while the Y201-C constructs were characterized by an increased ACAN expression. The approach we presented allows a standardizable production of spheroids with predictable geometry and the creation of a reproducible scaffold-free in vitro AC-like construct showing high expression of chondrogenic markers, using both HC and Y201-C. In addition, the bankable Y201-C cells provide an effective base model for experimentation with the spheroid approach to further enhance the process. Impact statement This is first work on the development of a repeatable scaffold-free in vitro model based on an optimized protocol in line with a recent clinically approved Chondrosphere® (CO.DON AG) technique. In addition, we demonstrated that a bankable cell type (Y201-C) could produce an engineered cartilage-like construct, giving a repeatable model as a key tool for experimentation of therapeutic treatment ahead of studies with heterogeneous cell populations.

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Tissue Engineering Part A
Tissue Engineering Part A CELL & TISSUE ENGINEERING-BIOTECHNOLOGY & APPLIED MICROBIOLOGY
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