Meniscus-Derived Matrix Scaffolds Promote the Integrative Repair of Meniscal Defects.
dc.contributor.author | Ruprecht, Jacob C | |
dc.contributor.author | Waanders, Taylor D | |
dc.contributor.author | Rowland, Christopher R | |
dc.contributor.author | Nishimuta, James F | |
dc.contributor.author | Glass, Katherine A | |
dc.contributor.author | Stencel, Jennifer | |
dc.contributor.author | DeFrate, Louis E | |
dc.contributor.author | Guilak, Farshid | |
dc.contributor.author | Weinberg, J Brice | |
dc.contributor.author | McNulty, Amy L | |
dc.date.accessioned | 2019-07-01T13:14:42Z | |
dc.date.available | 2019-07-01T13:14:42Z | |
dc.date.issued | 2019-06-18 | |
dc.date.updated | 2019-07-01T13:14:40Z | |
dc.description.abstract | Meniscal tears have a poor healing capacity, and damage to the meniscus is associated with significant pain, disability, and progressive degenerative changes in the knee joint that lead to osteoarthritis. Therefore, strategies to promote meniscus repair and improve meniscus function are needed. The objective of this study was to generate porcine meniscus-derived matrix (MDM) scaffolds and test their effectiveness in promoting meniscus repair via migration of endogenous meniscus cells from the surrounding meniscus or exogenously seeded human bone marrow-derived mesenchymal stem cells (MSCs). Both endogenous meniscal cells and MSCs infiltrated the MDM scaffolds. In the absence of exogenous cells, the 8% MDM scaffolds promoted the integrative repair of an in vitro meniscal defect. Dehydrothermal crosslinking and concentration of the MDM influenced the biochemical content and shear strength of repair, demonstrating that the MDM can be tailored to promote tissue repair. These findings indicate that native meniscus cells can enhance meniscus healing if a scaffold is provided that promotes cellular infiltration and tissue growth. The high affinity of cells for the MDM and the ability to remodel the scaffold reveals the potential of MDM to integrate with native meniscal tissue to promote long-term repair without necessarily requiring exogenous cells. | |
dc.identifier | 10.1038/s41598-019-44855-3 | |
dc.identifier.issn | 2045-2322 | |
dc.identifier.issn | 2045-2322 | |
dc.identifier.uri | ||
dc.language | eng | |
dc.publisher | Springer Science and Business Media LLC | |
dc.relation.ispartof | Scientific reports | |
dc.relation.isversionof | 10.1038/s41598-019-44855-3 | |
dc.title | Meniscus-Derived Matrix Scaffolds Promote the Integrative Repair of Meniscal Defects. | |
dc.type | Journal article | |
duke.contributor.orcid | DeFrate, Louis E|0000-0002-6982-349X | |
duke.contributor.orcid | Weinberg, J Brice|0000-0003-4052-5576 | |
duke.contributor.orcid | McNulty, Amy L|0000-0003-0556-0106 | |
pubs.begin-page | 8719 | |
pubs.issue | 1 | |
pubs.organisational-group | School of Medicine | |
pubs.organisational-group | Duke | |
pubs.organisational-group | Duke Cancer Institute | |
pubs.organisational-group | Institutes and Centers | |
pubs.organisational-group | Immunology | |
pubs.organisational-group | Basic Science Departments | |
pubs.organisational-group | Duke Global Health Institute | |
pubs.organisational-group | University Institutes and Centers | |
pubs.organisational-group | Institutes and Provost's Academic Units | |
pubs.organisational-group | Obstetrics and Gynecology | |
pubs.organisational-group | Clinical Science Departments | |
pubs.organisational-group | Medicine, Hematology | |
pubs.organisational-group | Medicine | |
pubs.publication-status | Published | |
pubs.volume | 9 |
Files
Original bundle
- Name:
- Sci Rep MenisMay2019.pdf
- Size:
- 1.64 MB
- Format:
- Adobe Portable Document Format
- Description:
- Accepted version