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体外构建的骨软骨模型作为研究骨关节炎环境的工具。

An In Vitro Engineered Osteochondral Model as Tool to Study Osteoarthritis Environment.

机构信息

School of Engineering, Newcastle University, Newcastle upon Tyne, NE1 7RU, UK.

Department of Clinical and Molecular Sciences (DISCLIMO), Università Politecnica delle Marche, Ancona, 60126, Italy.

出版信息

Adv Healthc Mater. 2023 Jan;12(2):e2202030. doi: 10.1002/adhm.202202030. Epub 2022 Oct 27.

Abstract

Osteoarthritis (OA) is a joint degenerative pathology characterized by mechanical and inflammatory damages affecting synovium, articular cartilage (AC), and subchondral bone (SB). Several in vitro, in vivo, and ex vivo models are developed to study OA, but to date the identification of specific pharmacological targets seems to be hindered by the lack of models with predictive capabilities. This study reports the development of a biomimetic in vitro model of AC and SB interface. Gellan gum methacrylated and chondroitin sulfate/dopamine hydrogels are used for the AC portion, whereas polylactic acid functionalized with gelatin and nanohydroxyapatite for the SB. The physiological behavior of immortalized stem cells (Y201s) and Y201s differentiated in chondrocytes (Y201-Cs), respectively, for the SB and AC, is demonstrated over 21 days of culture in vitro in healthy and pathological conditions, whilst modeling the onset of cytokines-induced OA. The key metrics are: lower glycosaminoglycans production and increased calcification given by a higher Collagen X content, in the AC deep layer; higher expression of pro-angiogenic factor (vegf) and decreased expression of osteogenic markers (coll1, spp1, runx2) in the SB. This novel approach provides a new tool for studying the development and progression of OA.

摘要

骨关节炎(OA)是一种关节退行性病变,其特征为影响滑膜、关节软骨(AC)和软骨下骨(SB)的机械和炎症损伤。已经开发了几种体外、体内和离体模型来研究 OA,但迄今为止,由于缺乏具有预测能力的模型,特定的药物靶点似乎难以确定。本研究报告了一种仿生 AC 和 SB 界面的体外模型的开发。甲基化的葡聚糖胶和硫酸软骨素/多巴胺水凝胶用于 AC 部分,而用明胶和纳米羟基磷灰石功能化的聚乳酸用于 SB。在体外健康和病理条件下培养 21 天,分别对 SB 和 AC 中的永生化干细胞(Y201s)和分化为软骨细胞的 Y201s(Y201-Cs)进行了生理行为研究,同时模拟了细胞因子诱导的 OA 的发病。关键指标是:在 AC 深层,糖胺聚糖产量降低,Collagen X 含量增加,导致钙化增加;SB 中的促血管生成因子(vegf)表达增加,成骨标志物(coll1、spp1、runx2)表达降低。这种新方法为研究 OA 的发展和进展提供了一种新工具。

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