Positive Regulation of Osteoblast Proliferation and Differentiation in MC3T3- E1 Cells by 7,3',4'-Trimethoxyflavone

Curr Mol Pharmacol. 2024:17:e18761429305367. doi: 10.2174/0118761429305367240725112731.

Abstract

Objectives: Increasing ratio of bone fragility, and susceptibility to fractures constitutes a major health problem worldwide. Therefore, we aimed to identify new compounds with a potential to increase proliferation and differentiation of osteoblasts.

Methods: Cellular and molecular assays, such as ALP activity, alizarin staining, and flow cytometry were employed to check the effect of TMF on osteogenesis. Moreover, gene expression analysis of certain important genes and transcriptional factors was also performed.

Results: Our findings report for the first time that 7,3',4'-trimethoxyflavone is capable of enhancing proliferation, and differentiation in osteoblast cells. Results from flow cytometry analysis also indicated that TMF increases the number of cells in S-phase. Furthermore, treatment with TMF altered the expression of osteogenic genes, OCN and Axin-2 indicating possible activation of Wnt signaling pathway.

Conclusion: Taken together, this study identified that 7,3',4'-trimethoxyflavone has the potential to enhance osteoblast proliferation and differentiation, possibly due to the activation of Wnt/β-catenin pathway. Thus, demonstrating TMF as naturally occurring agent to promote osteogenesis and prevention of bone fragility, and related disorders.

Keywords: 73′4′-Trimethoxyflavone; Bone fragility; MC3T3-E1; Osteoblast; Wnt/β-catenin..

MeSH terms

  • Animals
  • Axin Protein / metabolism
  • Cell Differentiation* / drug effects
  • Cell Line
  • Cell Proliferation* / drug effects
  • Flavones* / pharmacology
  • Flavonoids / pharmacology
  • Mice
  • Osteoblasts* / cytology
  • Osteoblasts* / drug effects
  • Osteoblasts* / metabolism
  • Osteogenesis* / drug effects
  • Wnt Signaling Pathway* / drug effects
  • beta Catenin / metabolism

Substances

  • Flavones
  • Axin Protein
  • Flavonoids
  • beta Catenin
  • Axin2 protein, mouse