Low-Level Laser Irradiation Promotes Proliferation and Differentiation on Apical Papilla Stem Cells

Author:

Gutiérrez David1ORCID,Rouabhia Mahmoud2ORCID,Ortiz Javiera3ORCID,Gaviria Diego4,Alfonso Camilo5ORCID,Muñoz Ana67ORCID,Inostroza Carolina8ORCID

Affiliation:

1. Faculty of dentistry, Buccal Innovation research group, Antonio Nariño University, Bogotá, Colombia

2. Faculty of Dentistry, Laval University, Quebec, Canada

3. Centro de Investigación e Innovación Biomédica (CIIB), Faculty of Medicine, Universidad de los Andes, Santiago, Chile

4. Artek Laser Dentistry, Bogotá, Colombia

5. Faculty of Dentistry, Research Group of Oral Health, Antonio Nariño University, Bogotá, Colombia

6. Faculty of Science, Cellular and Functional Biology and Biomolecule Engineering Research Group, Antonio Nariño University, Bogotá, Colombia

7. Hemolife National Blood Bank Foundation

8. Center for Research and Biomedical Innovation (CIIB), Faculty of Medicine, Universidad de los Andes, Santiago, Chile

Abstract

Introduction: Low-level laser therapy (LLLT) has been reported to improve cell proliferation and differentiation. The stem cells derived from dental apical papilla (SCAPs) are a promising therapy because they are easily obtained from immature human teeth. The effect of LLLT over SCAPs is still unknown. This study aimed to evaluate the proliferation and osteogenic potential of the SCAPs stimulated with LLLT. Methods: SCAPs were isolated from the third molars of a healthy donor and characterized according to the minimum established criteria. SCAPs were cultured for 24 hours before being exposed to LLLT. Cells were exposed to different doses, energy, and wavelengths for selecting the irradiation parameters. SCAPs proliferation was evaluated with the MTT assay at 24 hours and 7-day post-laser exposure. VEGF and TGFβ2 expression were assessed with a specific enzyme-linked immunosorbent assay (ELISA). The osteogenic differentiation potential was analyzed with alizarin red staining, and the nodule quantification was performed by the relative optical density (ROD) analysis using ImageJ software. Results: The cells isolated from the apical papilla showed phenotype and stem cell properties. SCAPs irradiated with one dose at 6 J/m2 and 650 nm exhibited significantly higher proliferation (P>0.05) than the controls nonirradiated. LLLT stimulated SCAPs’ expression of factors VEGF and TGFβ2. Also, SCAPs irradiated showed higher osteogenic activity (P<0.05). Conclusion: LLLT promotes proliferation, osteogenic differentiation, and VEGF and TGFβ2 expression on SCAPs. LLLT is a practical approach for the preconditioning of SCAPs in vitro for future regenerative therapies. More studies are needed to determine the underlying molecular processes that determine the mechanism of the LLLT.

Publisher

Maad Rayan Publishing Company

Subject

Urology,Nephrology,Dermatology,Dentistry (miscellaneous),Orthopedics and Sports Medicine,Surgery

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