Meniscus-Derived Matrix Bioscaffolds: Effects of Concentration and Cross-Linking on Meniscus Cellular Responses and Tissue Repair.

dc.contributor.authorLyons, Lucas P
dc.contributor.authorHidalgo Perea, Sofia
dc.contributor.authorWeinberg, J Brice
dc.contributor.authorWittstein, Jocelyn R
dc.contributor.authorMcNulty, Amy L
dc.date.accessioned2020-01-01T15:31:17Z
dc.date.available2020-01-01T15:31:17Z
dc.date.issued2019-12-19
dc.date.updated2020-01-01T15:31:15Z
dc.description.abstractMeniscal injuries, particularly in the avascular zone, have a low propensity for healing and are associated with the development of osteoarthritis. Current meniscal repair techniques are limited to specific tear types and have significant risk for failure. In previous work, we demonstrated the ability of meniscus-derived matrix (MDM) scaffolds to augment the integration and repair of an in vitro meniscus defect. The objective of this study was to determine the effects of percent composition and dehydrothermal (DHT) or genipin cross-linking of MDM bioscaffolds on primary meniscus cellular responses and integrative meniscus repair. In all scaffolds, the porous microenvironment allowed for exogenous cell infiltration and proliferation, as well as endogenous meniscus cell migration. The genipin cross-linked scaffolds promoted extracellular matrix (ECM) deposition and/or retention. The shear strength of integrative meniscus repair was improved with increasing percentages of MDM and genipin cross-linking. Overall, the 16% genipin cross-linked scaffolds were most effective at enhancing integrative meniscus repair. The ability of the genipin cross-linked scaffolds to attract endogenous meniscus cells, promote glycosaminoglycan and collagen deposition, and enhance integrative meniscus repair reveals that these MDM scaffolds are promising tools to augment meniscus healing.
dc.identifierijms21010044
dc.identifier.issn1422-0067
dc.identifier.issn1422-0067
dc.identifier.urihttps://hdl.handle.net/10161/19673
dc.languageeng
dc.publisherMDPI AG
dc.relation.ispartofInternational journal of molecular sciences
dc.relation.isversionof10.3390/ijms21010044
dc.subjectbiomechanical
dc.subjectcartilage
dc.subjectfibrochondrocyte
dc.subjectjoint
dc.subjectknee
dc.subjectproteoglycan
dc.subjectregeneration
dc.subjecttissue engineering
dc.titleMeniscus-Derived Matrix Bioscaffolds: Effects of Concentration and Cross-Linking on Meniscus Cellular Responses and Tissue Repair.
dc.typeJournal article
duke.contributor.idWeinberg, J Brice|0115187
duke.contributor.idWittstein, Jocelyn R|0312234
duke.contributor.idMcNulty, Amy L|0226708
duke.contributor.orcidWeinberg, J Brice|0000-0003-4052-5576
duke.contributor.orcidMcNulty, Amy L|0000-0003-0556-0106
pubs.begin-page44
pubs.end-page44
pubs.issue1
pubs.organisational-groupSchool of Medicine
pubs.organisational-groupDuke
pubs.organisational-groupDuke Cancer Institute
pubs.organisational-groupInstitutes and Centers
pubs.organisational-groupImmunology
pubs.organisational-groupBasic Science Departments
pubs.organisational-groupDuke Global Health Institute
pubs.organisational-groupUniversity Institutes and Centers
pubs.organisational-groupInstitutes and Provost's Academic Units
pubs.organisational-groupObstetrics and Gynecology
pubs.organisational-groupClinical Science Departments
pubs.organisational-groupMedicine, Hematology
pubs.organisational-groupMedicine
pubs.publication-statusPublished
pubs.volume21

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