Title |
Chondroitin sulfate-tyramine-based hydrogels for cartilage tissue repair / |
Authors |
Uzielienė, Ilona ; Bironaitė, Daiva ; Pachaleva, Jolita ; Bagdonas, Edvardas ; Sobolev, Arkadij ; Tsai, Wei-Bor ; Kvedaras, Giedrius ; Bernotienė, Eiva |
DOI |
10.3390/ijms24043451 |
Full Text |
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Is Part of |
International journal of molecular sciences.. Basel : MDPI. 2023, vol. 24, iss. 4, art. no. 3451, p. 1-19.. ISSN 1661-6596. eISSN 1422-0067 |
Keywords [eng] |
bone marrow mesenchymal stem cells ; chondroitin sulfate tyramine hydrogels ; cartilage oligomeric matrix protein ; mechanical compression/load ; biointegration ; cartilage regeneration |
Abstract [eng] |
The degradation of cartilage, due to trauma, mechanical load or diseases, results in abundant loss of extracellular matrix (ECM) integrity and development of osteoarthritis (OA). Chondroitin sulfate (CS) is a member of the highly sulfated glycosaminoglycans (GAGs) and a primary component of cartilage tissue ECM. In this study, we aimed to investigate the effect of mechanical load on the chondrogenic differentiation of bone marrow mesenchymal stem cells (BM-MCSs) encapsulated into CS-tyramine-gelatin (CS-Tyr/Gel) hydrogel in order to evaluate the suitability of this composite for OA cartilage regeneration studies in vitro. The CS-Tyr/Gel/BM-MSCs composite showed excellent biointegration on cartilage explants. The applied mild mechanical load stimulated the chondrogenic differentiation of BM-MSCs in CS-Tyr/Gel hydrogel (immunohistochemical collagen II staining). However, the stronger mechanical load had a negative effect on the human OA cartilage explants evaluated by the higher release of ECM components, such as the cartilage oligomeric matrix protein (COMP) and GAGs, compared to the not-compressed explants. Finally, the application of the CS-Tyr/Gel/BM-MSCs composite on the top of the OA cartilage explants decreased the release of COMP and GAGs from the cartilage explants. Data suggest that the CS-Tyr/Gel/BM-MSCs composite can protect the OA cartilage explants from the damaging effects of external mechanical stimuli. Therefore, it can be used for investigation of OA cartilage regenerative potential and mechanisms under the mechanical load in vitro with further perspectives of therapeutic application in vivo. |
Published |
Basel : MDPI |
Type |
Journal article |
Language |
English |
Publication date |
2023 |
CC license |
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