Osteoblastic differentiation and changes in the redox state in pulp stem cells by laser treatment

Lasers Med Sci. 2024 Mar 6;39(1):87. doi: 10.1007/s10103-024-04016-z.

Abstract

The aim of this study was to determine the effect of low-level laser therapy (LLLT) on cell proliferation, mitochondrial membrane potential changes (∆Ψm), reactive oxygen species (ROS), and osteoblast differentiation of human dental pulp stem cells (hDPSCs). These cells were irradiated with 660- and 940-nm lasers for 5 s, 50 s, and 180 s. Cell proliferation was assessed using the resazurin assay, cell differentiation by RUNX2 and BMP2 expression, and the presence of calcification nodules using alizarin-red S staining. ROS was determined by the dichlorofluorescein-diacetate technique and changes in ∆Ψm by the tetramethylrhodamine-ester assay. Data were analyzed by a Student's t-test and Mann-Whitney U test. The 940-nm wavelength for 5 and 50 s increased proliferation at 4 days postirradiation. After 8 days, a significant decrease in proliferation was observed in all groups. Calcification nodules were evident in all groups, with a greater staining intensity in cells treated with a 940-nm laser for 50 s, an effect that correlated with increased RUNX2 and BMP2 expression. ROS production and Δψm increased independently of irradiation time. In conclusion, photobiomodulation (PBM) with LLLT induced morphological changes and reduced cell proliferation rate, which was associated with osteoblastic differentiation and increased ROS and Δψm, independent of wavelength and time.

Keywords: Human dental pulp stem cells; Low-level laser therapy; Osteoblast differentiation; Photobiomodulation; Reactive oxygen species.

MeSH terms

  • Calcinosis*
  • Cell Differentiation
  • Core Binding Factor Alpha 1 Subunit*
  • Humans
  • Oxidation-Reduction
  • Reactive Oxygen Species
  • Stem Cells

Substances

  • Core Binding Factor Alpha 1 Subunit
  • Reactive Oxygen Species