Effects of Compression on Extracellular Matrix Synthesis by Chondrocytes and Chondrosarcoma Cells.

IF 2.6 4区 医学 Q1 ORTHOPEDICS
Carlo Alberto Paggi, Isa Porsul, Séverine Le Gac, Marcel Karperien
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Abstract

ObjectiveMechanical loading is critical for chondrocyte function and cartilage matrix production, yet its effects on clustered chondrocytes in end-stage osteoarthritis and on chondrosarcoma cells remain poorly understood. This study investigated how cyclic compression influences chondrocytes and chondrosarcoma cells cultured either as single cells or as micromasses.MethodsAn organ-on-chip platform was used to apply cyclic compression to chondrocytes and chondrosarcoma cells embedded in agarose as single cells or micromasses mimicking chondrocyte clusters. Deformation during loading was assessed, and after four days of stimulation, gene and protein expression of cartilage markers and extracellular matrix components were analyzed.ResultsChondrocyte micromasses deformed less than single cells and showed behavior resembling chondrosarcoma cells and their micromasses. All four culture models exhibited distinct mechanobiological responses after four days of compression. Mechanical loading promoted collagen I reorganization in micromasses and increased ACAN and COL2A1 expression, with enhanced matrix deposition aligned with the loading direction in one chondrocyte donor and one chondrosarcoma cell line. Semi-quantitative imaging suggested trends toward ECM deposition along the loading axis in some micromass conditions.ConclusionIn this agarose-based organ-on-chip proof-of-concept model, cellular organization was associated with distinct responses to cyclic compression. These findings should be interpreted as model-specific observations from one OA donor and one chondrosarcoma cell line, and require validation in additional donors, cell lines, matrices, and loading conditions before broader conclusions can be drawn.

压缩对软骨细胞和软骨肉瘤细胞合成细胞外基质的影响。
力学载荷对软骨细胞功能和软骨基质的生成至关重要,但其对终末期骨关节炎和软骨肉瘤细胞聚集性软骨细胞的影响尚不清楚。本研究探讨了循环压缩对单细胞或微团培养的软骨细胞和软骨肉瘤细胞的影响。方法采用器官芯片平台对琼脂糖包埋的软骨细胞和软骨肉瘤细胞作为单细胞或模拟软骨细胞簇的微团进行循环压缩。评估加载过程中的变形,并在刺激4天后分析软骨标志物和细胞外基质成分的基因和蛋白质表达。结果软骨细胞微团的变形小于单个细胞,表现出与软骨肉瘤细胞及其微团相似的行为。经过4天的压缩,所有4种培养模型都表现出明显的机械生物学反应。在一个软骨细胞供体和一个软骨肉瘤细胞系中,机械负荷促进了胶原I在微团中的重组,增加了ACAN和COL2A1的表达,基质沉积增强,与负荷方向一致。半定量成像显示,在某些微质量条件下,ECM有沿加载轴沉积的趋势。在这个基于琼脂糖的器官芯片概念验证模型中,细胞组织与循环压缩的不同反应有关。这些发现应该被解释为来自一个OA供体和一个软骨肉瘤细胞系的模型特异性观察结果,并且需要在其他供体、细胞系、基质和加载条件中进行验证,才能得出更广泛的结论。
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来源期刊
CARTILAGE
CARTILAGE ORTHOPEDICS-
CiteScore
6.90
自引率
7.10%
发文量
80
期刊介绍: CARTILAGE publishes articles related to the musculoskeletal system with particular attention to cartilage repair, development, function, degeneration, transplantation, and rehabilitation. The journal is a forum for the exchange of ideas for the many types of researchers and clinicians involved in cartilage biology and repair. A primary objective of CARTILAGE is to foster the cross-fertilization of the findings between clinical and basic sciences throughout the various disciplines involved in cartilage repair. The journal publishes full length original manuscripts on all types of cartilage including articular, nasal, auricular, tracheal/bronchial, and intervertebral disc fibrocartilage. Manuscripts on clinical and laboratory research are welcome. Review articles, editorials, and letters are also encouraged. The ICRS envisages CARTILAGE as a forum for the exchange of knowledge among clinicians, scientists, patients, and researchers. The International Cartilage Repair Society (ICRS) is dedicated to promotion, encouragement, and distribution of fundamental and applied research of cartilage in order to permit a better knowledge of function and dysfunction of articular cartilage and its repair.
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