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dc.contributor.authorLuo, Len_US
dc.contributor.authorO'Reilly, ARen_US
dc.contributor.authorThorpe, SDen_US
dc.contributor.authorBuckley, CTen_US
dc.contributor.authorKelly, DJen_US
dc.date.accessioned2016-12-12T12:36:53Z
dc.date.available2016-01-29en_US
dc.date.issued2017-09en_US
dc.date.submitted2016-12-07T15:18:32.751Z
dc.identifier.urihttp://qmro.qmul.ac.uk/xmlui/handle/123456789/18194
dc.description.abstractEngineering tissues with a structure and spatial composition mimicking those of native articular cartilage (AC) remains a challenge. This study examined if infrapatellar fat pad-derived stem cells (FPSCs) can be used to engineer cartilage grafts with a bulk composition and a spatial distribution of matrix similar to the native tissue. In an attempt to mimic the oxygen gradients and mechanical environment within AC, FPSC-laden hydrogels (either 2 mm or 4 mm in height) were confined to half of their thickness and/or subjected to dynamic compression (DC). Confining FPSC-laden hydrogels was predicted to accentuate the gradient in oxygen tension through the depth of the constructs (higher in the top and lower in the bottom), leading to enhanced glycosaminoglycan (GAG) and collagen synthesis in 2 mm high tissues. When subjected to DC alone, both GAG and collagen accumulation increased within 2 mm high unconfined constructs. Furthermore, the dynamic modulus of constructs increased from 0.96 MPa to 1.45 MPa following the application of DC. There was no synergistic benefit of coupling confinement and DC on overall levels of matrix accumulation; however in all constructs, irrespective of their height, the combination of these boundary conditions led to the development of engineered tissues that spatially best resembled native AC. The superficial region of these constructs mimicked that of native tissue, staining weakly for GAG, strongly for type II collagen, and in 4 mm high tissues more intensely for proteoglycan 4 (lubricin). This study demonstrated that FPSCs respond to joint-like environmental conditions by producing cartilage tissues mimicking native AC. Copyright © 2016 John Wiley & Sons, Ltd.en_US
dc.description.sponsorshipEuropean Research Council Starter Grant. Grant Number: 258463en_US
dc.format.extent2613 - 2628en_US
dc.languageengen_US
dc.relation.ispartofJ Tissue Eng Regen Meden_US
dc.rightsThis is a pre-copyedited, author-produced PDF of an article accepted for publication in Journal of Tissue Engineering and Regenerative Medicine following peer review. The version of record is available http://onlinelibrary.wiley.com/doi/10.1002/term.2162/full
dc.subjectcartilage tissue engineeringen_US
dc.subjectconfinementen_US
dc.subjectdynamic compressionen_US
dc.subjectmechanical environmenten_US
dc.subjectoxygenen_US
dc.subjectproteoglycan 4en_US
dc.subjectAdipose Tissueen_US
dc.subjectAnimalsen_US
dc.subjectCartilageen_US
dc.subjectCompressive Strengthen_US
dc.subjectHydrogelsen_US
dc.subjectOxygenen_US
dc.subjectStem Cellsen_US
dc.subjectStress, Mechanicalen_US
dc.subjectSwineen_US
dc.subjectTissue Engineeringen_US
dc.titleEngineering zonal cartilaginous tissue by modulating oxygen levels and mechanical cues through the depth of infrapatellar fat pad stem cell laden hydrogels.en_US
dc.typeArticle
dc.rights.holderCopyright © 2016 John Wiley & Sons, Ltd.
dc.identifier.doi10.1002/term.2162en_US
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/27138274en_US
pubs.issue9en_US
pubs.notesNo embargoen_US
pubs.publication-statusPublisheden_US
pubs.volume11en_US
dcterms.dateAccepted2016-01-29en_US


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