Please use this identifier to cite or link to this item:
http://hdl.handle.net/10397/113656
| DC Field | Value | Language |
|---|---|---|
| dc.contributor | Department of Biomedical Engineering | en_US |
| dc.creator | Kwan, KYC | en_US |
| dc.creator | Li, K | en_US |
| dc.creator | Wang, YY | en_US |
| dc.creator | Tse, WY | en_US |
| dc.creator | Tong, CY | en_US |
| dc.creator | Zhang, X | en_US |
| dc.creator | Wang, DM | en_US |
| dc.creator | Ker, DFE | en_US |
| dc.date.accessioned | 2025-06-17T01:33:59Z | - |
| dc.date.available | 2025-06-17T01:33:59Z | - |
| dc.identifier.uri | http://hdl.handle.net/10397/113656 | - |
| dc.language.iso | en | en_US |
| dc.publisher | MDPI AG | en_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.rights | The 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.subject | Dexamethasone | en_US |
| dc.subject | Fibrocartilage tissue engineering | en_US |
| dc.subject | Glucose | en_US |
| dc.subject | Growth factors | en_US |
| dc.subject | Human mesenchymal stem cells | en_US |
| dc.subject | Serum-free medium | en_US |
| dc.title | The characterization of serum-free media on human mesenchymal stem cell fibrochondrogenesis | en_US |
| dc.type | Journal/Magazine Article | en_US |
| dc.identifier.volume | 12 | en_US |
| dc.identifier.issue | 5 | en_US |
| dc.identifier.doi | 10.3390/bioengineering12050546 | en_US |
| dcterms.abstract | Developing 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.accessRights | open access | en_US |
| dcterms.bibliographicCitation | Bioengineering, May 2025, v. 12, no. 5, 546 | en_US |
| dcterms.isPartOf | Bioengineering | en_US |
| dcterms.issued | 2025-05 | - |
| dc.identifier.scopus | 2-s2.0-105006787804 | - |
| dc.identifier.eissn | 2306-5354 | en_US |
| dc.identifier.artn | 546 | en_US |
| dc.description.validate | 202506 bcwc | en_US |
| dc.description.oa | Version of Record | en_US |
| dc.identifier.FolderNumber | a3710 | - |
| dc.identifier.SubFormID | 50816 | - |
| dc.description.fundingSource | RGC | en_US |
| dc.description.fundingSource | Others | en_US |
| dc.description.fundingText | National 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 University | en_US |
| dc.description.pubStatus | Published | en_US |
| dc.description.oaCategory | CC | en_US |
| Appears in Collections: | Journal/Magazine Article | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| bioengineering-12-00546-v2.pdf | 1.91 MB | Adobe PDF | View/Open |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.



