Bioenergetics of photobiomodulated osteoblast mitochondrial cells derived from human pulp stem cells: systematic review

Lasers Med Sci. 2022 Apr;37(3):1843-1853. doi: 10.1007/s10103-021-03439-2. Epub 2021 Nov 22.

Abstract

Dental pulp cells are a source of multipotent mesenchymal stem cells with a high proliferation rate and multilineage differentiation potential. This study investigated the photobiomodulated bioenergetic effects of mitochondria in osteoblasts that differentiated from human pulp stem cells. The systematic review followed PRISMA guidelines. The PICO question was formulated. Criteria for inclusion and exclusion were established prior to searches being performed on the PubMed/MEDLINE, Embase, and Scopus. Articles were identified and included if published in English within last 10 years; photobiomodulation or low-level laser therapy were discussed; the delivery parameters for dose and time were included and the studies focused on bioenergetics of osteoblast mitochondria. Studies excluded were non-human dental pulp tissue and in vivo studies. A total number of 110 articles were collated, 106 were excluded leaving a total of 4 articles. These studies demonstrated that in vitro use of photobiomodulation was performed using different laser and LED types; InGaAlP; InGaN; and InGaAsP with average wavelengths of 630 to 940 nm. Primary human osteoblastic STRO-1 and mesenchymal stem cell lineages were studied. Three out of four articles confirmed positive bioenergetic effects of photobiomodulation on mitochondria of osteoblasts derived from human pulp cells. This systematic review demonstrated a lack of adequate reporting of bioenergetics of osteoblast mitochondria after photobiomodulation treatment.

Keywords: Bioenergetics; Bone regeneration; Dental pulp stem cells; Low-level laser therapy (LLLT); Mitochondria; Photobiomodulation (PBM).

Publication types

  • Systematic Review

MeSH terms

  • Cell Differentiation
  • Cell Proliferation
  • Dental Pulp
  • Energy Metabolism
  • Humans
  • Low-Level Light Therapy*
  • Mitochondria
  • Osteoblasts
  • Stem Cells*