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Effect of Photobiomodulation Therapy on Differentiation of Mesenchymal Stem Cells Derived From Impacted Third Molar Tooth Into Neuron-Like Cells Publisher Pubmed



Mohammadi F1, 2 ; Bahrami N1, 3 ; Nazariyan M4 ; Mohamadnia A5, 6 ; Hakimiha N7 ; Nazariyan A8
Authors
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Authors Affiliations
  1. 1. Craniomaxillofacial Research Center, Tehran University of Medical Sciences, Tehran, Iran
  2. 2. Oral and Maxillofacial Surgery Department, School of Dentistry, Tehran University of Medical Sciences, Tehran, Iran
  3. 3. Department of Tissue Engineering, School of Advanced Technologies in Medicine, Tehran University of Medical Sciences, Tehran, Iran
  4. 4. School of Dentistry, Tehran University of Medical Sciences, Tehran, Iran
  5. 5. Chronic Respiratory Diseases Research Center, National Research Institute of Tuberculosis and Lung Diseases (NRITLD), Shahid Beheshti University of Medical Sciences, Tehran, Iran
  6. 6. Department of Biotechnology, School of Advanced Technologies in Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran
  7. 7. Laser Application in Medical Sciences Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran
  8. 8. Clinical biochemistry Department, Faculty of Medicine, Zanjan University of Medical Sciences, Tehran, Iran

Source: Photochemistry and Photobiology Published:2022


Abstract

Peripheral nerve damages are among the most important consequences of dental and maxillofacial procedures. Tissue engineering using mesenchymal stem cells (MSCs) is a promising method to manage such injuries. Moreover, photobiomodulation therapy (PBMT) can enhance this treatment. The present study aimed to investigate the effect of PBMT on differentiation of MSCs derived from dental follicle (DF) into neurons. MSCs were isolated from an impacted tooth follicle by digestion method. The stem cells were cultured, and differentiated into neurons. The cells received two sessions of PBMT with 810 or 980 nm diode laser (100 mW, 4 J cm−2) in either DMEM or neural inductive medium. Phenotypic characterization of the cells was determined using flow cytometry. In addition, β-tubulin and MAP2 genes expression level changes were analyzed using RT-PCR and western blot technique. After 14 days, flow cytometry analysis confirmed the mesenchymal nature of cells. RT-PCR and western blot affirmed the expression of β-tubulin and MAP2 genes and proteins respectively. PBMT with both wavelengths significantly increased β-tubulin and MAP2 expression in neural inductive medium with highest expression mean in 980 nm group. PBMT with 810 and 980 nm lasers could be a promising adjunctive method in differentiation of DF-originated MSCs into neural cells. © 2022 American Society for Photobiology.
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