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Effect of periostin on bone metabolic and autophagy factors during tooth eruption in mice

This study aimed to investigate the effect of periostin (PN) on the expression of receptor activator of nuclear factor-κB ligand (RANKL), osteoprotegerin (OPG), microtubule-associated protein1 light chain 3B (LC3B), and Beclin1 in mouse alveolar bone specimens and cultured osteoblasts in vitro, to p...

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Autores principales: Qin, Han, Cai, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: De Gruyter 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10426264/
https://www.ncbi.nlm.nih.gov/pubmed/37589010
http://dx.doi.org/10.1515/biol-2022-0663
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author Qin, Han
Cai, Jun
author_facet Qin, Han
Cai, Jun
author_sort Qin, Han
collection PubMed
description This study aimed to investigate the effect of periostin (PN) on the expression of receptor activator of nuclear factor-κB ligand (RANKL), osteoprotegerin (OPG), microtubule-associated protein1 light chain 3B (LC3B), and Beclin1 in mouse alveolar bone specimens and cultured osteoblasts in vitro, to preliminarily explore the role of PN and autophagy in remodeling bone metabolism during tooth eruption. Mice at 5 days of age were injected with 75 ng/mL recombinant PN protein under the periosteum for 3 consecutive days according to the standard of 1 mL/100 g/day. Then, their mandibles were removed, and the expression of bone metabolic and autophagy factors was detected by immunohistochemistry. Mouse osteoblast-like cells cultured in vitro were treated with recombinant PN at a concentration of 75 ng/mL. The changes in the aforementioned indicators were compared again by immunofluorescence and western blotting 72 h after dosing. The results of the mouse samples showed that the protein expression of RANKL, LC3B, and Beclin1 decreased, accompanied by the decrease in RANKL/OPG ratio. However, OPG protein expression increased in the dosing group. Immunofluorescence and western blotting results of osteoblasts cultured in vitro showed that the protein expression of RANKL, LC3B, Beclin1, and the RANKL/OPG ratio in the experimental group decreased, but OPG expression increased. PN may regulate alveolar bone metabolism during tooth eruption by inhibiting the RANKL/OPG ratio and autophagy, which will provide a new research perspective for further exploration of the mechanisms during tooth eruption.
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spelling pubmed-104262642023-08-16 Effect of periostin on bone metabolic and autophagy factors during tooth eruption in mice Qin, Han Cai, Jun Open Life Sci Research Article This study aimed to investigate the effect of periostin (PN) on the expression of receptor activator of nuclear factor-κB ligand (RANKL), osteoprotegerin (OPG), microtubule-associated protein1 light chain 3B (LC3B), and Beclin1 in mouse alveolar bone specimens and cultured osteoblasts in vitro, to preliminarily explore the role of PN and autophagy in remodeling bone metabolism during tooth eruption. Mice at 5 days of age were injected with 75 ng/mL recombinant PN protein under the periosteum for 3 consecutive days according to the standard of 1 mL/100 g/day. Then, their mandibles were removed, and the expression of bone metabolic and autophagy factors was detected by immunohistochemistry. Mouse osteoblast-like cells cultured in vitro were treated with recombinant PN at a concentration of 75 ng/mL. The changes in the aforementioned indicators were compared again by immunofluorescence and western blotting 72 h after dosing. The results of the mouse samples showed that the protein expression of RANKL, LC3B, and Beclin1 decreased, accompanied by the decrease in RANKL/OPG ratio. However, OPG protein expression increased in the dosing group. Immunofluorescence and western blotting results of osteoblasts cultured in vitro showed that the protein expression of RANKL, LC3B, Beclin1, and the RANKL/OPG ratio in the experimental group decreased, but OPG expression increased. PN may regulate alveolar bone metabolism during tooth eruption by inhibiting the RANKL/OPG ratio and autophagy, which will provide a new research perspective for further exploration of the mechanisms during tooth eruption. De Gruyter 2023-08-08 /pmc/articles/PMC10426264/ /pubmed/37589010 http://dx.doi.org/10.1515/biol-2022-0663 Text en © 2023 the author(s), published by De Gruyter https://creativecommons.org/licenses/by/4.0/This work is licensed under the Creative Commons Attribution 4.0 International License.
spellingShingle Research Article
Qin, Han
Cai, Jun
Effect of periostin on bone metabolic and autophagy factors during tooth eruption in mice
title Effect of periostin on bone metabolic and autophagy factors during tooth eruption in mice
title_full Effect of periostin on bone metabolic and autophagy factors during tooth eruption in mice
title_fullStr Effect of periostin on bone metabolic and autophagy factors during tooth eruption in mice
title_full_unstemmed Effect of periostin on bone metabolic and autophagy factors during tooth eruption in mice
title_short Effect of periostin on bone metabolic and autophagy factors during tooth eruption in mice
title_sort effect of periostin on bone metabolic and autophagy factors during tooth eruption in mice
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10426264/
https://www.ncbi.nlm.nih.gov/pubmed/37589010
http://dx.doi.org/10.1515/biol-2022-0663
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