Carlo Alberto Paggi, Isa Porsul, Séverine Le Gac, Marcel Karperien
{"title":"Effects of Compression on Extracellular Matrix Synthesis by Chondrocytes and Chondrosarcoma Cells.","authors":"Carlo Alberto Paggi, Isa Porsul, Séverine Le Gac, Marcel Karperien","doi":"10.1177/19476035261460455","DOIUrl":null,"url":null,"abstract":"<p><p>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 <b>ACAN</b> and <b>COL2A1</b> 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.</p>","PeriodicalId":9626,"journal":{"name":"CARTILAGE","volume":" ","pages":"19476035261460455"},"PeriodicalIF":2.6000,"publicationDate":"2026-07-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13379520/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"CARTILAGE","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1177/19476035261460455","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ORTHOPEDICS","Score":null,"Total":0}
引用次数: 0
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.
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.