The effect of citric acid on mineralisation and vascular endothelial growth factor secretion from apical papilla stem cells

Authors

  • Krasimir Hristov Department of Pediatric Dentistry, Faculty of Dental Medicine, Medical University of Sofia, Sofia, Bulgaria
  • Nikolay Ishkitiev Department of Chemistry and Biochemistry, Medical Faculty, Medical University of Sofia, Sofia, Bulgaria
  • Marina Miteva Department of Chemistry and Biochemistry, Medical Faculty, Medical University of Sofia, Sofia, Bulgaria
  • Violeta Dimitrova Department of Chemistry and Biochemistry, Medical Faculty, Medical University of Sofia, Sofia, Bulgaria
  • Ralitsa Gigova Department of Pediatric Dentistry, Faculty of Dental Medicine, Medical University of Sofia, Sofia, Bulgaria
  • Nataliya Gateva Department of Pediatric Dentistry, Faculty of Dental Medicine, Medical University of Sofia, Sofia, Bulgaria
  • Liliya Angelova Department of Dental Public Health, Faculty of Dental Medicine, Medical University of Sofia, Sofia, Bulgaria

DOI:

https://doi.org/10.2340/aos.v83.42026

Keywords:

Citric acid, VEGF, regenerative endodontics, stem cells from apical papilla, immature teeth

Abstract

Objective: To investigate the influence of citric acid on the osteogenic and angiogenic potential of stem cells from apical papillae (SCAPs).

Materials and methods: Stem cells from apical papillae were isolated from freshly extracted third permanent molars. These cells were treated with 20 and 100 μM citric acid. Alizarin red staining was used to evaluate mineral deposition. The secreted levels of vascular endothelial growth factor (VEGF) were assessed by ELISA on days 18, 24 and 28. Immunofluorescence analysis was performed to assess the expression of surface markers after exposure to 20 and 100 μM citric acid.

Results: Different mineralisation patterns were observed. Supplemented with citric acid, media showed more diffuse and less dense crystals. On day 18, most VEGF was secreted from the cells with no added citric acid. On day 24, there was a significant increase (p < 0.05) in the levels of VEGF secreted from cells treated with 20 μM citric acid. On day 28, cells from the control group did not secrete VEGF. There was a reduction in the levels of VEGF secreted by cells treated with 20 μM citric acid and a significant increase in the cells exposed to 100 μM citric acid (p < 0.05).

Conclusion: Citric acid can promote the differentiation of SCAPs and angiogenesis.

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References

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Published

2024-10-01