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基于软骨球的无支架方法制造关节软骨模型。

A Chondrosphere-Based Scaffold Free Approach to Manufacture an Articular Cartilage Model.

机构信息

School of Engineering, Newcastle University, Newcastle Upon Tyne, United Kingdom.

Translational and Clinical Research Institute, Newcastle University, Newcastle Upon Tyne, United Kingdom.

出版信息

Tissue Eng Part A. 2022 Jan;28(1-2):84-93. doi: 10.1089/ten.TEA.2021.0061. Epub 2021 Aug 25.

Abstract

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 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/cm), 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 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 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.

摘要

人关节软骨(AC)的工程是再生医学的一个挑战。本研究的主要目的是开发一种可重复的无支架模型,用于基于软骨细胞球体的软骨缺陷治疗,以允许对这种类型的治疗进行系统研究和进一步优化。培养人关节软骨细胞(HC)和永生化间充质细胞分化为软骨细胞(Y201-Cs),在平底 96 孔板中生成细胞球体,并在 7 天的培养过程中评估其生长动力学和活力。然后,根据与临床批准的软骨球(CO.DON AG)技术一致的方案,将球体组装并在明胶包被的聚乳酸-共-羟基乙酸(PLGA)电纺膜上培养 21 天(每平方厘米 10 个球体)。HC 和 Y201-C 细胞在培养 7 天后形成了紧凑且有活力的球体,直径在 7 天内从 1300±150μm 减小到 600±90μm 和从 1250±60μm 减小到 800±20μm。当球体转移到支撑膜上时,它们会粘附在膜本身并融合,根据基因表达和糖胺聚糖定量分析,产生 II 型胶原(COL2A1)和聚集蛋白聚糖(ACAN)。我们检测到 HC 细胞中 COL2A1 的表达更高,而 Y201-C 构建物的特征是 ACAN 表达增加。我们提出的方法允许使用可预测几何形状的标准化球体生产,并使用 HC 和 Y201-C 构建具有高表达软骨形成标志物的可重复无支架 AC 样构建体。此外,可储存的 Y201-C 细胞为使用球体方法进一步增强该过程的实验提供了有效的基础模型。 影响声明 这是第一项关于开发基于与最近临床批准的软骨球(CO.DON AG)技术一致的优化方案的可重复无支架模型的工作。此外,我们证明了一种可储存的细胞类型(Y201-C)可以产生工程软骨样构建体,提供了一种可重复的模型,作为实验治疗的关键工具,为使用异质细胞群体进行研究之前。

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