Meniscus-Derived Matrix Bioscaffolds: Effects of Concentration and Cross-Linking on Meniscus Cellular Responses and Tissue Repair.
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.
Type
Journal articlePermalink
https://hdl.handle.net/10161/19673Published Version (Please cite this version)
10.3390/ijms21010044Publication Info
Lyons, Lucas P; Hidalgo Perea, Sofia; Weinberg, J Brice; Wittstein, Jocelyn R; & McNulty,
Amy L (2019). Meniscus-Derived Matrix Bioscaffolds: Effects of Concentration and Cross-Linking on
Meniscus Cellular Responses and Tissue Repair. International journal of molecular sciences, 21(1). pp. 44-44. 10.3390/ijms21010044. Retrieved from https://hdl.handle.net/10161/19673.This is constructed from limited available data and may be imprecise. To cite this
article, please review & use the official citation provided by the journal.
Collections
More Info
Show full item recordScholars@Duke
Amy Lynn McNulty
Associate Professor in Orthopaedic Surgery
The McNulty Lab is working to develop strategies to prevent osteoarthritis and to
promote tissue repair and regeneration following joint injury. In order to accomplish
this, we are working in three main areas. 1) We are working to understand the pathways
that are activated by normal and injurious mechanical loading of cartilage and meniscus
and how these mechanotransduction pathways are altered during aging, injury, and tissue
degeneration. A greater understanding of alterations in mech
Joe Brice Weinberg
Professor of Medicine
Dr. Weinberg is a board-certified hematologist and medical oncologist who serves as
Professor of Medicine and Immunology and Associate Professor of Obstetrics and Gynecology
at the Duke University Medical Center, and staff physician in hematology-oncology
at the Durham V.A. Medical Center. His clinical interests are in hematology and oncology,
and his research focuses on blood cells, nitric oxide (NO), and leukemia. The work
includes studies of resistance to infection, pathways of inflamm
Jocelyn Ross Wittstein
Associate Professor of Orthopaedic Surgery
Alphabetical list of authors with Scholars@Duke profiles.

Articles written by Duke faculty are made available through the campus open access policy. For more information see: Duke Open Access Policy
Rights for Collection: Scholarly Articles
Works are deposited here by their authors, and represent their research and opinions, not that of Duke University. Some materials and descriptions may include offensive content. More info