Mitochondrial Oxygen Consumption and Immunocytochemistry of Human Dental Pulp Stem Cell Following 808 nm PBM Therapy: A 3D Cell Culture Study

J Biophotonics. 2025 Sep;18(9):e70051. doi: 10.1002/jbio.70051. Epub 2025 Apr 28.

Abstract

This study investigated the impact of 808 nm laser photobiomodulation (PBM) on mitochondrial respiration and osteogenic protein expression (OCN, OPN, ALP, RUNX2, COL-1, BMP-2) in human dental pulp stem cells (hDPSCs) within a 3D hydrogel model. hDPSCs were isolated from third molars and maintained under hypoxic conditions. Cells received PBM at 5 and 15 J/cm2 using an 808 nm diode laser. The study showed that 808 nm PBM can alter mitochondrial respiration, with 5 J/cm2 enhancing osteogenic protein expression (OCN, ALP, OPN, RUNX2) but failing to sustain BMP-2 at 24 h. In contrast, 15 J/cm2 induced stronger upregulation and prolonged BMP-2 expression, suggesting an optimal dose for sustained osteogenic activity. BMP-2 was later downregulated, and COL-1 remained unchanged post-PBM. Importantly, this study indicates the dose-specific PBM modulation of mitochondrial respiration and protein expression, but further research is required to optimize treatment protocols.

Keywords: human dental pulp stem cells; hypoxic microenvironment; mitochondrial oxygen consumption; photobiomodulation; seahorse extracellular flux analyzer.

MeSH terms

  • Cell Culture Techniques, Three Dimensional*
  • Dental Pulp* / cytology
  • Humans
  • Immunohistochemistry
  • Low-Level Light Therapy*
  • Mitochondria* / metabolism
  • Mitochondria* / radiation effects
  • Osteogenesis / radiation effects
  • Oxygen Consumption* / radiation effects
  • Stem Cells* / cytology
  • Stem Cells* / metabolism
  • Stem Cells* / radiation effects