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Defining the Most Potent Osteoinductive Culture Conditions for MC3T3-E1 Cells Reveals No Implication of Oxidative Stress or Energy Metabolism

Overview
Journal Int J Mol Sci
Publisher MDPI
Date 2024 Apr 27
PMID 38673767
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Abstract

The MC3T3-E1 preosteoblastic cell line is widely utilised as a reliable in vitro system to assess bone formation. However, the experimental growth conditions for these cells hugely diverge, and, particularly, the osteogenic medium (OSM)'s composition varies in research studies. Therefore, we aimed to define the ideal culture conditions for MC3T3-E1 subclone 4 cells with regard to their mineralization capacity and explore if oxidative stress or the cellular metabolism processes are implicated. Cells were treated with nine different combinations of long-lasting ascorbate (Asc) and β-glycerophosphate (βGP), and osteogenesis/calcification was evaluated at three different time-points by qPCR, Western blotting, and bone nodule staining. Key molecules of the oxidative and metabolic pathways were also assessed. It was found that sufficient mineral deposition was achieved only in the 150 μg.mL/2 mM Asc/βGP combination on day 21 in OSM, and this was supported by , , , and expression level increases. NOX2 and SOD2 as well as PGC1α and Tfam were also monitored as indicators of redox and metabolic processes, respectively, where no differences were observed. Elevation in OCN protein levels and ALP activity showed that mineralisation comes as a result of these differences. This work defines the most appropriate culture conditions for MC3T3-E1 cells and could be used by other research laboratories in this field.

References
1.
Mostafa N, Fitzsimmons R, Major P, Adesida A, Jomha N, Jiang H . Osteogenic differentiation of human mesenchymal stem cells cultured with dexamethasone, vitamin D3, basic fibroblast growth factor, and bone morphogenetic protein-2. Connect Tissue Res. 2011; 53(2):117-31. DOI: 10.3109/03008207.2011.611601. View

2.
Krause U, Seckinger A, Gregory C . Assays of osteogenic differentiation by cultured human mesenchymal stem cells. Methods Mol Biol. 2011; 698:215-30. DOI: 10.1007/978-1-60761-999-4_17. View

3.
Qiu C, Li Z, Peng P . Human umbilical cord mesenchymal stem cells protect MC3T3-E1 osteoblasts from dexamethasone-induced apoptosis via induction of the Nrf2-ARE signaling pathway. Regen Ther. 2024; 27:1-11. PMC: 10926296. DOI: 10.1016/j.reth.2024.02.009. View

4.
Pihlajaniemi T, Myllyla R, Kivirikko K . Prolyl 4-hydroxylase and its role in collagen synthesis. J Hepatol. 1991; 13 Suppl 3:S2-7. DOI: 10.1016/0168-8278(91)90002-s. View

5.
Wenstrup R, Fowlkes J, Witte D, Florer J . Discordant expression of osteoblast markers in MC3T3-E1 cells that synthesize a high turnover matrix. J Biol Chem. 1996; 271(17):10271-6. DOI: 10.1074/jbc.271.17.10271. View