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

dc.contributor.author

Lyons, Lucas P

dc.contributor.author

Hidalgo Perea, Sofia

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Weinberg, J Brice

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Wittstein, Jocelyn R

dc.contributor.author

McNulty, Amy L

dc.date.accessioned

2020-01-01T15:31:17Z

dc.date.available

2020-01-01T15:31:17Z

dc.date.issued

2019-12-19

dc.date.updated

2020-01-01T15:31:15Z

dc.description.abstract

Meniscal 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.identifier

ijms21010044

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1422-0067

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1422-0067

dc.identifier.uri

https://hdl.handle.net/10161/19673

dc.language

eng

dc.publisher

MDPI AG

dc.relation.ispartof

International journal of molecular sciences

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10.3390/ijms21010044

dc.subject

biomechanical

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cartilage

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fibrochondrocyte

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joint

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knee

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proteoglycan

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regeneration

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tissue engineering

dc.title

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

dc.type

Journal article

duke.contributor.orcid

Weinberg, J Brice|0000-0003-4052-5576

duke.contributor.orcid

McNulty, Amy L|0000-0003-0556-0106

pubs.begin-page

44

pubs.end-page

44

pubs.issue

1

pubs.organisational-group

School of Medicine

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Duke

pubs.organisational-group

Duke Cancer Institute

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Institutes and Centers

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Immunology

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Basic Science Departments

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Duke Global Health Institute

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University Institutes and Centers

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Institutes and Provost's Academic Units

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Obstetrics and Gynecology

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Clinical Science Departments

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Medicine, Hematology

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Medicine

pubs.publication-status

Published

pubs.volume

21

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