Effects of the combination of dexamethasone and fibroblast growth factor-2 on differentiation of osteoprecursor cells
Open accessAbstract
Dexamethasone is a potent modulator of osteogenic differentiation and previous studies have shown that dexamethasone increases the bone formation capacity of osteoprogenitor cells in vitro. Fibroblast growth factor‑2 (FGF‑2) is reported to have numerous biological activities, including stimulation of cell growth, migration, angiogenesis, wound healing, tissue repair, differentiation and morphogenesis. In the present study, the dose‑dependent effect of dexamethasone and FGF‑2 on the differentiation of osteoprecursor cells was evaluated. The alkaline phosphatase (ALP) activity test was performed to assess differentiation and protein expression associated with bone formation was measured by western blot analysis. The results showed that the protein content of the cultures grown with the osteogenic differentiation media in the presence of 2 ng/ml FGF‑2 was increased compared with that of the untreated control. ALP activity was increased when cells were treated with dexamethasone, with the highest value at 100 nM. The addition of 20 ng/ml FGF‑2 to 100 nM dexamethasone showed an increase in ALP activity, however, this was not statistically significant. The combination of 100 nM dexamethasone and 20 ng/ml FGF‑2 produced the highest expression of bone morphogenetic protein receptor‑IA and bone morphogenetic protein receptor‑II, leading to the highest value of pSmad1/5/8 expression. Within the limits of this study, dexamethasone significantly enhanced osteoblast differentiation, however, the combined delivery of dexamethasone and FGF‑2 did not produce synergistic effects on osteoblast differentiation under the current experimental conditions.
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Literature reports effective Dex concentrations for MC3T3-E1 ALP induction range from 10 to 100 nM, with optimal at 50 nM.
“Literature reports effective Dex concentrations for MC3T3-E1 ALP induction range from 10 to 100 nM [25,48,49], with optimal at 50 nM [50].”
From Functional Surface Modification of Magnesium Implant by Drug-Loaded Biodegradable Polymer Coating (2026) · cites this paper as [48]
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Functional Surface Modification of Magnesium Implant by Drug-Loaded Biodegradable Polymer Coating
Park, J.-E., Jang, Y.-S., Ko, S.-O., & Lee, M.-H. (2026) · Applied Sciences · doi:10.3390/app16031542 · Cited by 2 · see citing works
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- Authors
- PARK, J.-B.
- Affiliations
- The Catholic University of Korea Seoul St. Mary's Hospital (KR)
- Corresponding author
- PARK, JUN-BEOM
- Venue
- Molecular Medicine Reports
- Publisher
- Spandidos Publications
- Published
- 2013-11-19
- Volume
- 9
- Issue
- 2
- Pages
- 659-662
- ISSN
- 1791-2997 (ISSN-L)
- 1791-3004
- OpenAlex
- W2063062118
- Semantic Scholar
- 314360c1c6f52e0bf6533852491ffb5fa276529d
- Cited by
- 15
- References
- 19
- Citations by year
- 2026: 1 · 2025: 1 · 2023: 1 · 2022: 2 · 2021: 1 · 2020: 1 · 2018: 3 · 2017: 1 · 2016: 2 · 2015: 1 · 2014: 1
- FWCI
- 0.60
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Molecular Medicine Reports (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Catholic University of Korea
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bone Metabolism and Diseases
- Physical Sciences › Engineering › Biomedical Engineering › Bone Tissue Engineering Materials
- Health Sciences › Medicine › Genetics › Mesenchymal stem cell research
- Keywords
- dexamethasone, fibroblast growth factor 2, osteogenic differentiation, osteoprogenitor cells, alkaline phosphatase activity, Smad1/5/8 phosphorylation, synergistic effect, glucocorticoids, bone formation
- MeSH terms
- Alkaline Phosphatase, Animals, Cell Differentiation, Cells, Cultured, Dexamethasone, Drug Combinations, Humans, Osteogenesis, Transforming Growth Factor beta, Fibroblast Growth Factor 2, Gene Expression Regulation, Developmental, Bone Morphogenetic Proteins, Cell Proliferation, Mice
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