A multiscale framework for evaluating three-dimensional cell mechanics in fibril-reinforced poroelastic tissues with anatomical cell distribution – Analysis of chondrocyte deformation behavior in mechanically loaded articular cartilage

dc.contributor.authorTanska P
dc.contributor.authorVenäläinen MS
dc.contributor.authorErdemir A
dc.contributor.authorKorhonen RK
dc.contributor.organizationfi=Turun biotiedekeskus|en=Turku Bioscience Centre|
dc.contributor.organization-code1.2.246.10.2458963.20.18586209670
dc.converis.publication-id46142252
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/46142252
dc.date.accessioned2022-10-27T12:16:44Z
dc.date.available2022-10-27T12:16:44Z
dc.description.abstractCharacterization of the mechanical environment of cells in collagenous biological tissues during different daily activities is crucial for understanding the role of mechanics on cell biosynthesis and tissue health. However, current imaging methods are limited in characterizing very fast deformations of cells. This could be achieved with computational multiscale modeling, but current models accommodating collagen fibril networks and poroelastic ground matrix have included only a single cell. In this study, a workflow was developed for generating a three-dimensional multiscale model with imaging-based anatomical cell distributions and their micro-environment (pericellular and extracellular matrix). Fibril-reinforced poroelastic material models with (FRPES) and without (FRPE) swelling were implemented into the model and simulations were performed for evaluating cell deformations before and after experimental loading conducted for rabbit knee joint cartilage. We observed that the cells experienced considerably different deformation based on their location in all models. Both FRPE and FRPES models were able to predict the trends in the changes in cell deformations, although the average and median magnitudes differed between the model predictions and experiments. However, the FRPES model results were generally closer to the experimental results. Current findings suggest that morphological properties of cells are affected by the variations in the tissue properties between the samples and variations within the sample caused by the measurement geometry, local structure and composition. Thus, it would be important to consider the anatomical distribution and location of multiple cells along with the structure of fibril networks if cell deformation metrics are evaluated in collagenous tissues. (C) 2020 The Author(s). Published by Elsevier Ltd.
dc.identifier.jour-issn0021-9290
dc.identifier.olddbid174406
dc.identifier.oldhandle10024/157500
dc.identifier.urihttps://www.utupub.fi/handle/11111/34227
dc.identifier.urnURN:NBN:fi-fe2021042822919
dc.language.isoen
dc.okm.affiliatedauthorVenäläinen, Mikko
dc.okm.discipline318 Medical biotechnologyen_GB
dc.okm.discipline318 Lääketieteen bioteknologiafi_FI
dc.okm.internationalcopublicationinternational co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherELSEVIER SCI LTD
dc.publisher.countryUnited Kingdomen_GB
dc.publisher.countryBritanniafi_FI
dc.publisher.country-codeGB
dc.relation.articlenumberUNSP 109648
dc.relation.doi10.1016/j.jbiomech.2020.109648
dc.relation.ispartofjournalJournal of Biomechanics
dc.relation.volume101
dc.source.identifierhttps://www.utupub.fi/handle/10024/157500
dc.titleA multiscale framework for evaluating three-dimensional cell mechanics in fibril-reinforced poroelastic tissues with anatomical cell distribution – Analysis of chondrocyte deformation behavior in mechanically loaded articular cartilage
dc.year.issued2020

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