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Effects of Red LED Irradiation in Enhancing the Mineralization of Human Dental Pulp Cells In Vitro

Dentin regeneration is the preferred method used to preserve dental pulp vitality after pulp exposure due to caries. Red light-emitting diode irradiation (LEDI), which is based on photobiomodulation (PBM), has been used to promote hard-tissue regeneration. However, the underlying mechanism still nee...

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Autores principales: Yang, Ying, Kim, Ok-Su, Liu, Guo, Lee, Bin-Na, Liu, Danyang, Fu, Wenqi, Zhu, Siyu, Kang, Jae-Seok, Kim, Byunggook, Kim, Okjoon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10253352/
https://www.ncbi.nlm.nih.gov/pubmed/37298716
http://dx.doi.org/10.3390/ijms24119767
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author Yang, Ying
Kim, Ok-Su
Liu, Guo
Lee, Bin-Na
Liu, Danyang
Fu, Wenqi
Zhu, Siyu
Kang, Jae-Seok
Kim, Byunggook
Kim, Okjoon
author_facet Yang, Ying
Kim, Ok-Su
Liu, Guo
Lee, Bin-Na
Liu, Danyang
Fu, Wenqi
Zhu, Siyu
Kang, Jae-Seok
Kim, Byunggook
Kim, Okjoon
author_sort Yang, Ying
collection PubMed
description Dentin regeneration is the preferred method used to preserve dental pulp vitality after pulp exposure due to caries. Red light-emitting diode irradiation (LEDI), which is based on photobiomodulation (PBM), has been used to promote hard-tissue regeneration. However, the underlying mechanism still needs elucidation. This study aimed to explore the mechanism involved in red LEDI affecting dentin regeneration. Alizarin red S (ARS) staining revealed that red LEDI induced mineralization of human dental pulp cells (HDPCs) in vitro. We further distinguished the cell proliferation (0–6 d), differentiation (6–12 d), and mineralization (12–18 d) of HDPCs in vitro and treated cells either with or without red LEDI in each stage. The results showed that red LEDI treatment in the mineralization stage, but not the proliferation or differentiation stages, increased mineralized nodule formation around HDPCs. Western blot also indicated that red LEDI treatment in the mineralization stage, but not the proliferation or differentiation stages, upregulated the expression of dentin matrix marker proteins (dentin sialophosphoprotein, DSPP; dentin matrix protein 1, DMP1; osteopontin, OPN) and an intracellular secretory vesicle marker protein (lysosomal-associated membrane protein 1, LAMP1). Therefore, the red LEDI might enhance the matrix vesicle secretion of HDPCs. On the molecular level, red LEDI enhanced mineralization by activating the mitogen-activated protein kinase (MAPK) signaling pathways (ERK and P38). ERK and P38 inhibition reduced mineralized nodule formation and the expression of relevant marker proteins. In summary, red LEDI enhanced the mineralization of HDPCs by functioning to produce a positive effect in the mineralization stage in vitro.
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spelling pubmed-102533522023-06-10 Effects of Red LED Irradiation in Enhancing the Mineralization of Human Dental Pulp Cells In Vitro Yang, Ying Kim, Ok-Su Liu, Guo Lee, Bin-Na Liu, Danyang Fu, Wenqi Zhu, Siyu Kang, Jae-Seok Kim, Byunggook Kim, Okjoon Int J Mol Sci Article Dentin regeneration is the preferred method used to preserve dental pulp vitality after pulp exposure due to caries. Red light-emitting diode irradiation (LEDI), which is based on photobiomodulation (PBM), has been used to promote hard-tissue regeneration. However, the underlying mechanism still needs elucidation. This study aimed to explore the mechanism involved in red LEDI affecting dentin regeneration. Alizarin red S (ARS) staining revealed that red LEDI induced mineralization of human dental pulp cells (HDPCs) in vitro. We further distinguished the cell proliferation (0–6 d), differentiation (6–12 d), and mineralization (12–18 d) of HDPCs in vitro and treated cells either with or without red LEDI in each stage. The results showed that red LEDI treatment in the mineralization stage, but not the proliferation or differentiation stages, increased mineralized nodule formation around HDPCs. Western blot also indicated that red LEDI treatment in the mineralization stage, but not the proliferation or differentiation stages, upregulated the expression of dentin matrix marker proteins (dentin sialophosphoprotein, DSPP; dentin matrix protein 1, DMP1; osteopontin, OPN) and an intracellular secretory vesicle marker protein (lysosomal-associated membrane protein 1, LAMP1). Therefore, the red LEDI might enhance the matrix vesicle secretion of HDPCs. On the molecular level, red LEDI enhanced mineralization by activating the mitogen-activated protein kinase (MAPK) signaling pathways (ERK and P38). ERK and P38 inhibition reduced mineralized nodule formation and the expression of relevant marker proteins. In summary, red LEDI enhanced the mineralization of HDPCs by functioning to produce a positive effect in the mineralization stage in vitro. MDPI 2023-06-05 /pmc/articles/PMC10253352/ /pubmed/37298716 http://dx.doi.org/10.3390/ijms24119767 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Yang, Ying
Kim, Ok-Su
Liu, Guo
Lee, Bin-Na
Liu, Danyang
Fu, Wenqi
Zhu, Siyu
Kang, Jae-Seok
Kim, Byunggook
Kim, Okjoon
Effects of Red LED Irradiation in Enhancing the Mineralization of Human Dental Pulp Cells In Vitro
title Effects of Red LED Irradiation in Enhancing the Mineralization of Human Dental Pulp Cells In Vitro
title_full Effects of Red LED Irradiation in Enhancing the Mineralization of Human Dental Pulp Cells In Vitro
title_fullStr Effects of Red LED Irradiation in Enhancing the Mineralization of Human Dental Pulp Cells In Vitro
title_full_unstemmed Effects of Red LED Irradiation in Enhancing the Mineralization of Human Dental Pulp Cells In Vitro
title_short Effects of Red LED Irradiation in Enhancing the Mineralization of Human Dental Pulp Cells In Vitro
title_sort effects of red led irradiation in enhancing the mineralization of human dental pulp cells in vitro
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10253352/
https://www.ncbi.nlm.nih.gov/pubmed/37298716
http://dx.doi.org/10.3390/ijms24119767
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