<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>4(1)</volume><submitter>Timmermans RGM</submitter><pubmed_abstract>&lt;h4>Objective&lt;/h4>Due to the complexity and heterogeneity of osteoarthritis (OA) pathophysiology, studying the interaction between intrinsic molecular changes in chondrocytes after hyper-physiological mechanical stress (MS) and aberrant signalling of OA risk genes remains a challenge. In this study we set out to set up an &lt;i>in vitro&lt;/i> 3D neo cartilage pellet model that enables us to explore the responses of OA risk genes to hyper-physiological MS.&lt;h4>Design&lt;/h4>Human primary chondrocyte neo-cartilage pellets were exposed for 2 days to 2 ​× ​10 ​min of hyper-physiological dynamic MS attained by a 20% strain and a frequency of 5 ​Hz. In order to assess cartilage damage, sulphated glycosaminoglycan (sGAG) content in the neo-cartilage was quantified using Alcian blue staining and a dimethyl</pubmed_abstract><journal>Osteoarthritis and cartilage open</journal><pagination>100231</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9718246</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>A human &lt;i>in vitro&lt;/i> 3D neo-cartilage model to explore the response of OA risk genes to hyper-physiological mechanical stress.</pubmed_title><pmcid>PMC9718246</pmcid><pubmed_authors>Tuerlings M</pubmed_authors><pubmed_authors>Ramos YFM</pubmed_authors><pubmed_authors>Timmermans RGM</pubmed_authors><pubmed_authors>Bloks NGC</pubmed_authors><pubmed_authors>Meulenbelt I</pubmed_authors><pubmed_authors>van Hoolwerff M</pubmed_authors><pubmed_authors>van der Wal RJP</pubmed_authors><pubmed_authors>van den Bosch MHJ</pubmed_authors><pubmed_authors>Nelissen RGHH</pubmed_authors><pubmed_authors>Blom AB</pubmed_authors><pubmed_authors>van der Kraan PM</pubmed_authors></additional><is_claimable>false</is_claimable><name>A human &lt;i>in vitro&lt;/i> 3D neo-cartilage model to explore the response of OA risk genes to hyper-physiological mechanical stress.</name><description>&lt;h4>Objective&lt;/h4>Due to the complexity and heterogeneity of osteoarthritis (OA) pathophysiology, studying the interaction between intrinsic molecular changes in chondrocytes after hyper-physiological mechanical stress (MS) and aberrant signalling of OA risk genes remains a challenge. In this study we set out to set up an &lt;i>in vitro&lt;/i> 3D neo cartilage pellet model that enables us to explore the responses of OA risk genes to hyper-physiological MS.&lt;h4>Design&lt;/h4>Human primary chondrocyte neo-cartilage pellets were exposed for 2 days to 2 ​× ​10 ​min of hyper-physiological dynamic MS attained by a 20% strain and a frequency of 5 ​Hz. In order to assess cartilage damage, sulphated glycosaminoglycan (sGAG) content in the neo-cartilage was quantified using Alcian blue staining and a dimethyl</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Mar</publication><modification>2026-05-29T04:34:49.395Z</modification><creation>2025-04-06T14:07:24.781Z</creation></dates><accession>S-EPMC9718246</accession><cross_references><pubmed>36474468</pubmed><doi>10.1016/j.ocarto.2021.100231</doi></cross_references></HashMap>