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Effect of TNF-α-Induced Sclerostin on Osteocytes during Orthodontic Tooth Movement

Osteocytes are abundant cells in bone, which contribute to bone maintenance. Osteocytes express receptor activator of nuclear factor kappa-B ligand (RANKL) and regulate osteoclast formation. Orthodontic tooth movement (OTM) occurs by osteoclast resorption of alveolar bone. Osteocyte-derived RANKL is...

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Autores principales: Ohori, Fumitoshi, Kitaura, Hideki, Marahleh, Aseel, Kishikawa, Akiko, Ogawa, Saika, Qi, Jiawei, Shen, Wei-Ren, Noguchi, Takahiro, Nara, Yasuhiko, Mizoguchi, Itaru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6612957/
https://www.ncbi.nlm.nih.gov/pubmed/31341915
http://dx.doi.org/10.1155/2019/9716758
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author Ohori, Fumitoshi
Kitaura, Hideki
Marahleh, Aseel
Kishikawa, Akiko
Ogawa, Saika
Qi, Jiawei
Shen, Wei-Ren
Noguchi, Takahiro
Nara, Yasuhiko
Mizoguchi, Itaru
author_facet Ohori, Fumitoshi
Kitaura, Hideki
Marahleh, Aseel
Kishikawa, Akiko
Ogawa, Saika
Qi, Jiawei
Shen, Wei-Ren
Noguchi, Takahiro
Nara, Yasuhiko
Mizoguchi, Itaru
author_sort Ohori, Fumitoshi
collection PubMed
description Osteocytes are abundant cells in bone, which contribute to bone maintenance. Osteocytes express receptor activator of nuclear factor kappa-B ligand (RANKL) and regulate osteoclast formation. Orthodontic tooth movement (OTM) occurs by osteoclast resorption of alveolar bone. Osteocyte-derived RANKL is critical in bone resorption during OTM. Additionally, tumor necrosis factor-α (TNF-α) is important in osteoclastogenesis during OTM. Sclerostin has been reported to enhance RANKL expression in the MLO-Y4 osteocyte-like cell line. This study investigated the effect of TNF-α on sclerostin expression in osteocytes during OTM. In vitro analysis of primary osteocytes, which were isolated from DMP1-Topaz mice by sorting the Topaz variant of GFP-positive cells, revealed that SOST mRNA expression was increased when osteocytes were cultured with TNF-α and that RANKL mRNA expression was increased when osteocytes were cultured with sclerostin. Moreover, the number of TRAP-positive cells was increased in osteocytes and osteoclast precursors cocultured with sclerostin. In vivo analysis of mouse calvariae that had been subcutaneously injected with phosphate-buffered saline (PBS) or TNF-α revealed that the number of TRAP-positive cells and the percentage of sclerostin-positive osteocytes were higher in the TNF-α group than in the PBS group. Furthermore, the level of SOST mRNA was increased by TNF-α. As an OTM model, a Ni-Ti closed-coil spring connecting the upper incisors and upper-left first molar was placed to move the first molar to the mesial direction in wild-type (WT) mice and TNF receptor 1- and 2-deficient (TNFRsKO) mice. After 6 days of OTM, the percentage of sclerostin-positive osteocytes on the compression side of the first molar in TNFRsKO mice was lower than that in WT mice. In this study, TNF-α increased sclerostin expression in osteocytes, and sclerostin enhanced RANKL expression in osteocytes. Thus, TNF-α may play an important role in sclerostin expression in osteocytes and enhance osteoclast formation during OTM.
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spelling pubmed-66129572019-07-24 Effect of TNF-α-Induced Sclerostin on Osteocytes during Orthodontic Tooth Movement Ohori, Fumitoshi Kitaura, Hideki Marahleh, Aseel Kishikawa, Akiko Ogawa, Saika Qi, Jiawei Shen, Wei-Ren Noguchi, Takahiro Nara, Yasuhiko Mizoguchi, Itaru J Immunol Res Research Article Osteocytes are abundant cells in bone, which contribute to bone maintenance. Osteocytes express receptor activator of nuclear factor kappa-B ligand (RANKL) and regulate osteoclast formation. Orthodontic tooth movement (OTM) occurs by osteoclast resorption of alveolar bone. Osteocyte-derived RANKL is critical in bone resorption during OTM. Additionally, tumor necrosis factor-α (TNF-α) is important in osteoclastogenesis during OTM. Sclerostin has been reported to enhance RANKL expression in the MLO-Y4 osteocyte-like cell line. This study investigated the effect of TNF-α on sclerostin expression in osteocytes during OTM. In vitro analysis of primary osteocytes, which were isolated from DMP1-Topaz mice by sorting the Topaz variant of GFP-positive cells, revealed that SOST mRNA expression was increased when osteocytes were cultured with TNF-α and that RANKL mRNA expression was increased when osteocytes were cultured with sclerostin. Moreover, the number of TRAP-positive cells was increased in osteocytes and osteoclast precursors cocultured with sclerostin. In vivo analysis of mouse calvariae that had been subcutaneously injected with phosphate-buffered saline (PBS) or TNF-α revealed that the number of TRAP-positive cells and the percentage of sclerostin-positive osteocytes were higher in the TNF-α group than in the PBS group. Furthermore, the level of SOST mRNA was increased by TNF-α. As an OTM model, a Ni-Ti closed-coil spring connecting the upper incisors and upper-left first molar was placed to move the first molar to the mesial direction in wild-type (WT) mice and TNF receptor 1- and 2-deficient (TNFRsKO) mice. After 6 days of OTM, the percentage of sclerostin-positive osteocytes on the compression side of the first molar in TNFRsKO mice was lower than that in WT mice. In this study, TNF-α increased sclerostin expression in osteocytes, and sclerostin enhanced RANKL expression in osteocytes. Thus, TNF-α may play an important role in sclerostin expression in osteocytes and enhance osteoclast formation during OTM. Hindawi 2019-06-24 /pmc/articles/PMC6612957/ /pubmed/31341915 http://dx.doi.org/10.1155/2019/9716758 Text en Copyright © 2019 Fumitoshi Ohori et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Ohori, Fumitoshi
Kitaura, Hideki
Marahleh, Aseel
Kishikawa, Akiko
Ogawa, Saika
Qi, Jiawei
Shen, Wei-Ren
Noguchi, Takahiro
Nara, Yasuhiko
Mizoguchi, Itaru
Effect of TNF-α-Induced Sclerostin on Osteocytes during Orthodontic Tooth Movement
title Effect of TNF-α-Induced Sclerostin on Osteocytes during Orthodontic Tooth Movement
title_full Effect of TNF-α-Induced Sclerostin on Osteocytes during Orthodontic Tooth Movement
title_fullStr Effect of TNF-α-Induced Sclerostin on Osteocytes during Orthodontic Tooth Movement
title_full_unstemmed Effect of TNF-α-Induced Sclerostin on Osteocytes during Orthodontic Tooth Movement
title_short Effect of TNF-α-Induced Sclerostin on Osteocytes during Orthodontic Tooth Movement
title_sort effect of tnf-α-induced sclerostin on osteocytes during orthodontic tooth movement
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6612957/
https://www.ncbi.nlm.nih.gov/pubmed/31341915
http://dx.doi.org/10.1155/2019/9716758
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