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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2019
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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. |
format | Online Article Text |
id | pubmed-6612957 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
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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