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dc.creatorMacBarb, R. F.en
dc.creatorPaschos, N. K.en
dc.creatorAbeug, R.en
dc.creatorMakris, E. A.en
dc.creatorHu, J. C.en
dc.creatorAthanasiou, K. A.en
dc.date.accessioned2015-11-23T10:38:18Z
dc.date.available2015-11-23T10:38:18Z
dc.date.issued2014
dc.identifier10.1089/ten.tea.2013.0694
dc.identifier.issn19373341
dc.identifier.urihttp://hdl.handle.net/11615/30467
dc.description.abstractTissue-engineered musculoskeletal soft tissues typically lack the appropriate mechanical robustness of their native counterparts, hindering their clinical applicability. With structure and function being intimately linked, efforts to capture the anatomical shape and matrix organization of native tissues are imperative to engineer functionally robust and anisotropic tissues capable of withstanding the biomechanically complex in vivo joint environment. The present study sought to tailor the use of passive axial compressive loading to drive matrix synthesis and reorganization within self-assembled, shape-specific fibrocartilaginous constructs, with the goal of developing functionally anisotropic neotissues. Specifically, shape-specific fibrocartilaginous neotissues were subjected to 0, 0.01, 0.05, or 0.1N axial loads early during tissue culture. Results found the 0.1-N load to significantly increase both collagen and glycosaminoglycan synthesis by 27% and 67%, respectively, and to concurrently reorganize the matrix by promoting greater matrix alignment, compaction, and collagen crosslinking compared with all other loading levels. These structural enhancements translated into improved functional properties, with the 0.1-N load significantly increasing both the relaxation modulus and Young's modulus by 96% and 255%, respectively, over controls. Finite element analysis further revealed the 0.1-N uniaxial load to induce multiaxial tensile and compressive strain gradients within the shape-specific neotissues, with maxima of 10.1%, 18.3%, and-21.8% in the XX-, YY-, and ZZ-directions, respectively. This indicates that strains created in different directions in response to a single axis load drove the observed anisotropic functional properties. Together, results of this study suggest that strain thresholds exist within each axis to promote matrix synthesis, alignment, and compaction within the shape-specific neotissues. Tailoring of passive axial loading, thus, presents as a simple, yet effective way to drive in vitro matrix development in shape-specific neotissues toward more closely achieving native structural and functional properties. © 2014 Mary Ann Liebert, Inc.en
dc.source.urihttp://www.scopus.com/inward/record.url?eid=2-s2.0-84915747165&partnerID=40&md5=009e581964877dcea164b18a808731c1
dc.subjectAlignmenten
dc.subjectAnisotropyen
dc.subjectAxial loadsen
dc.subjectCollagenen
dc.subjectCompactionen
dc.subjectElastic modulien
dc.subjectFinite element methoden
dc.subjectHistologyen
dc.subjectStrainen
dc.subjectTissue cultureen
dc.subjectAxial compressive loadingen
dc.subjectCollagen crosslinkingen
dc.subjectCompressive strainen
dc.subjectFunctional propertiesen
dc.subjectGlycosaminoglycansen
dc.subjectMatrix organizationsen
dc.subjectMechanical robustnessen
dc.subjectStructural enhancementsen
dc.subjectTissueen
dc.subjectcollagen type 1en
dc.subjectcollagen type 2en
dc.subjectglycosaminoglycanen
dc.subjectanimal cellen
dc.subjectanimal tissueen
dc.subjectArticleen
dc.subjectcartilaginous tissueen
dc.subjectcollagen synthesisen
dc.subjectcompressive strengthen
dc.subjectcontrolled studyen
dc.subjectfinite element analysisen
dc.subjectfractional anisotropyen
dc.subjectglycosaminoglycan metabolismen
dc.subjectin vitro studyen
dc.subjectin vivo studyen
dc.subjectnonhumanen
dc.subjectprotein cross linkingen
dc.subjectstructure activity relationen
dc.subjecttensile strengthen
dc.subjecttissue engineeringen
dc.subjecttissue structureen
dc.subjectYoung modulusen
dc.titlePassive strain-induced matrix synthesis and organization in shape-specific, cartilaginous neotissuesen
dc.typejournalArticleen


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