4.6 Article

Effect of photobiomodulation therapy on TGF-13 release from dentin, migration and viability of dental pulp stem cells in regenerative endodontics treatment: An ex vivo study

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ELSEVIER SCIENCE SA
DOI: 10.1016/j.jphotobiol.2023.112817

Keywords

Transforming growth factor beta1; Tissue engineering; Low level laser therapy; Photobiology; Ethylenediaminetetraacetic acid; Dentin

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This study investigated the effect of photobiomodulation (PBM) therapy using an 808 nm diode laser on cellular modulation mechanisms in regenerative endodontic procedures (REPs). The results showed that PBM treatment significantly increased cell viability and migration, and enhanced the release of TGF-131 from dentin.
Background and aim: Regenerative endodontic procedures (REPs) are oriented by the principles of tissue engi-neering, incorporating dental pulp stem cells (DPSC), crucial growth factors like Transforming growth factor-13 (TGF-131), and scaffolds to facilitate the regeneration of dental pulp tissues. The present study aimed to inves-tigate the effect of photobiomodulation (PBM) therapy, using an 808 nm diode laser on cellular modulation mechanisms in REPs. Method and material: A total of 108 human dentin discs obtained from intact single root teeth were randomly assigned into six groups (n = 8): 1. Positive control (EDTA), 2. PBM-1 (3 J/cm2), 3. PBM-2 (5 J/cm2), 4. EDTA+PBM-1, 5. EDTA+PBM-2, and 6. Negative control (NaOCl). Then, an extract solution was prepared from each disc and the concentration of released TGF-131 from the discs was measured using enzyme-linked immu-nosorbent assay (ELISA). Moreover, the extract solution was added to DPSC culture medium to evaluate cell viability and migration through MTT assay and scratch test, respectively.Result: The group exposed to PBM-1 showed the highest cell viability, while treatment with EDTA and EDTA+PBM-2 decreased cellular viability. Also, the PBM-treated groups showed significantly higher release of TGF-131 compared to the negative control. EDTA and EDTA+PBM-1 showed the highest release among all the groups. No significant difference was found between EDTA and EDTA+PBM-1, as well as between PBM-1 and PBM-2. Moreover, the PBM-1 group exhibited the highest migration after 24 h, which was significantly greater than other groups, except for the PBM-2 group.Conclusion: According to the obtained data, 808 nm mediated-PBM (3 J/cm2), both independently and in conjunction with EDTA, enhanced the release of TGF-131 from dentin and improved cell viability and migration of DPSCs. It seems that, PBM under the specific parameters employed in this study, could be an effective adjunctive therapy in REPs.

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