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dc.contributor.authorSilva, J C.
dc.contributor.authorMoura, C.S.
dc.contributor.authorBorrecho, G.
dc.contributor.authorAlves de Matos, A.P.
dc.contributor.authorJoaquim, M.
dc.contributor.authorCabral, S.
dc.contributor.authorLinhardt, Robert J.
dc.contributor.authorFerreira, F.C.
dc.date2021
dc.date.accessioned2022-06-27T15:38:39Z
dc.date.available2022-06-27T15:38:39Z
dc.date.issued2021
dc.identifier.citationEffects of glycosaminoglycan supplementation in the chondrogenic differentiation of bone marrow- and synovial- derived mesenchymal stem/stromal cells on 3D-extruded poly (ε-caprolactone) scaffolds, J C. Silva, C. S. Moura, G. Borrecho, A. P. Alves de Matos, Joaquim M. S. Cabral, R. J. Linhardt, F. C. Ferreira, International Journal of Polymeric Materials and Polymeric Biomaterials,70, 207–222, 2021.
dc.identifier.urihttps://doi.org/10.1080/00914037.2019.1706511
dc.identifier.urihttps://hdl.handle.net/20.500.13015/5469
dc.descriptionInternational Journal of Polymeric Materials and Polymeric Biomaterials,70, 207–222
dc.descriptionNote : if this item contains full text it may be a preprint, author manuscript, or a Gold OA copy that permits redistribution with a license such as CC BY. The final version is available through the publisher’s platform.
dc.description.abstractThe lack of effective and long-term treatments for articular cartilage defects has increased the interest for innovative tissue engineering strategies. Such approaches, combining cells, biomaterial matrices and external biochemical/physical cues, hold promise for generating fully functional cartilage tissue. Herein, this study aims at exploring the use of the major cartilage glycosaminoglycans (GAGs), chondroitin sulfate (CS) and hyaluronic acid (HA), as external biochemical cues to promote the chondrogenic differentiation of human bone marrow- and synovium-derived mesenchymal stem/stromal cells (hBMSC/hSMSC) on custom-made 3 D porous poly (ε-caprolactone) (PCL) scaffolds. The culture conditions, namely the chondrogenic medium and hypoxic environment (5% O2 tension), were firstly optimized by culturing hBMSCs on PCL scaffolds without GAG supplementation. For both MSC sources, GAG supplemented media, particularly with HA, promoted significantly cartilage-like extracellular matrix (ECM) production (higher sulfated GAG amounts) and chondrogenic gene expression. Remarkably, in contrast to tissues generated using hBMSCs, the hSMSC-based constructs showed decreased expression of hypertrophic marker COL X. Histological, immunohistochemical and transmission electron microscopy (TEM) analysis confirmed the presence of typical articular cartilage ECM components (GAGs, aggrecan, collagen fibers) in all the tissue constructs produced. Overall, our results highlight the potential of integrating GAG supplementation, hSMSCs and customizable 3 D scaffolds toward the fabrication of bioengineered cartilage tissue substitutes with reduced hypertrophy.
dc.description.urihttps://login.libproxy.rpi.edu/login?url=https://doi.org/10.1080/00914037.2019.1706511
dc.languageen_US
dc.language.isoENG
dc.relation.ispartofThe Linhardt Research Labs Online Collection
dc.relation.ispartofRensselaer Polytechnic Institute, Troy, NY
dc.relation.urihttps://harc.rpi.edu/
dc.subjectBiology
dc.subjectChemistry and chemical biology
dc.subjectChemical and biological engineering
dc.subjectBiomedical engineering
dc.titleEffects of glycosaminoglycan supplementation in the chondrogenic differentiation of bone marrow- and synovial- derived mesenchymal stem/stromal cells on 3D-extruded poly (ε-caprolactone) scaffolds
dc.typeArticle
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dcterms.isVersionOfhttps://doi.org/10.1080/00914037.2019.1706511
dc.rights.holderIn Copyright : this Item is protected by copyright and/or related rights. You are free to use this Item in any way that is permitted by the copyright and related rights legislation that applies to your use. For other uses you need to obtain permission from the rights-holder(s). https://rightsstatements.org/page/InC/1.0/
dc.creator.identifierhttps://orcid.org/0000-0003-2219-5833
dc.relation.departmentThe Linhardt Research Labs.
dc.relation.departmentThe Shirley Ann Jackson, Ph.D. Center for Biotechnology and Interdisciplinary Studies (CBIS)


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