Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/113656
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dc.contributorDepartment of Biomedical Engineeringen_US
dc.creatorKwan, KYCen_US
dc.creatorLi, Ken_US
dc.creatorWang, YYen_US
dc.creatorTse, WYen_US
dc.creatorTong, CYen_US
dc.creatorZhang, Xen_US
dc.creatorWang, DMen_US
dc.creatorKer, DFEen_US
dc.date.accessioned2025-06-17T01:33:59Z-
dc.date.available2025-06-17T01:33:59Z-
dc.identifier.urihttp://hdl.handle.net/10397/113656-
dc.language.isoenen_US
dc.publisherMDPI AGen_US
dc.rights© 2025 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).en_US
dc.rightsThe following publication Kwan, K.Y.C.; Li, K.; Wang, Y.Y.; Tse, W.Y.; Tong, C.Y.; Zhang, X.; Wang, D.M.; Ker, D.F.E. The Characterization of Serum-Free Media on Human Mesenchymal Stem Cell Fibrochondrogenesis. Bioengineering 2025, 12, 546 is available at https://doi.org/10.3390/bioengineering12050546.en_US
dc.subjectDexamethasoneen_US
dc.subjectFibrocartilage tissue engineeringen_US
dc.subjectGlucoseen_US
dc.subjectGrowth factorsen_US
dc.subjectHuman mesenchymal stem cellsen_US
dc.subjectSerum-free mediumen_US
dc.titleThe characterization of serum-free media on human mesenchymal stem cell fibrochondrogenesisen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.volume12en_US
dc.identifier.issue5en_US
dc.identifier.doi10.3390/bioengineering12050546en_US
dcterms.abstractDeveloping fibrochondrogenic serum-free media is important for regenerating diseased and injured fibrocartilage but no defined protocols exist. Towards this goal, we characterized the effect of four candidate fibrochondrogenic serum-free media containing transforming growth factor beta-3 (TGF-β3), insulin-like growth factor-1 (IGF-1), and fibroblast growth factor-2 (FGF-2) with high/low glucose and with/without dexamethasone on human mesenchymal stem cells (hMSCs) via proliferation and differentiation assays. In Ki67 proliferation assays, serum-free media containing low glucose and dexamethasone exhibited the highest growth. In gene expression assays, serum-free media containing low glucose and commercially available chondrogenic media (COM) induced high fibrochondrogenic transcription factor expression (scleraxis/SCX and SRY-Box Transcription Factor 9/SOX9) and extracellular matrix (ECM) protein levels (aggrecan/ACAN, collagen type I/COL1A1, and collagen type II/COL2A1), respectively. In immunofluorescence staining, serum-free media containing high glucose and COM induced high fibrochondrogenic transcription factor (SCX and SOX9) and ECM protein (COL1A1, COL2A1, and collagen type X/COL10A1) levels, respectively. In cytochemical staining, COM and serum-free media containing dexamethasone showed a high collagen content whereas serum-free media containing high glucose and dexamethasone exhibited high glycosaminoglycan (GAG) levels. Altogether, defined serum-free media containing high glucose exhibited the highest fibrochondrogenic potential. In summary, this work studied conditions conducive for fibrochondrogenesis, which may be further optimized for potential applications in fibrocartilage tissue engineering.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationBioengineering, May 2025, v. 12, no. 5, 546en_US
dcterms.isPartOfBioengineeringen_US
dcterms.issued2025-05-
dc.identifier.scopus2-s2.0-105006787804-
dc.identifier.eissn2306-5354en_US
dc.identifier.artn546en_US
dc.description.validate202506 bcwcen_US
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumbera3710-
dc.identifier.SubFormID50816-
dc.description.fundingSourceRGCen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextNational Natural Science Foundation of China/Research Grants Council Joint Research Scheme; Food and Health Bureau; InnoHK initiative of the Innovation and Technology Commission of the Hong Kong Special Administrative Region Government; Hong Kong Polytechnic Universityen_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
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