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Circadian Rhythm Regulates Development of Enamel in Mouse Mandibular First Molar
Rhythmic incremental growth lines and the presence of melatonin receptors were discovered in tooth enamel, suggesting possible role of circadian rhythm. We therefore hypothesized that circadian rhythm may regulate enamel formation through melatonin receptors. To test this hypothesis, we examined exp...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4975438/ https://www.ncbi.nlm.nih.gov/pubmed/27494172 http://dx.doi.org/10.1371/journal.pone.0159946 |
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author | Tao, Jiang Zhai, Yue Park, Hyun Han, Junli Dong, Jianhui Xie, Ming Gu, Ting Lewi, Keidren Ji, Fang Jia, William |
author_facet | Tao, Jiang Zhai, Yue Park, Hyun Han, Junli Dong, Jianhui Xie, Ming Gu, Ting Lewi, Keidren Ji, Fang Jia, William |
author_sort | Tao, Jiang |
collection | PubMed |
description | Rhythmic incremental growth lines and the presence of melatonin receptors were discovered in tooth enamel, suggesting possible role of circadian rhythm. We therefore hypothesized that circadian rhythm may regulate enamel formation through melatonin receptors. To test this hypothesis, we examined expression of melatonin receptors (MTs) and amelogenin (AMELX), a maker of enamel formation, during tooth germ development in mouse. Using qRT-PCR and immunocytochemistry, we found that mRNA and protein levels of both MTs and AMELX in normal mandibular first molar tooth germs increased gradually after birth, peaked at 3 or 4 day postnatal, and then decreased. Expression of MTs and AMELX by immunocytochemistry was significantly delayed in neonatal mice raised in all-dark or all-light environment as well as the enamel development. Furthermore, development of tooth enamel was also delayed showing significant immature histology in those animals, especially for newborn mice raised in all daylight condition. Interestingly, disruption in circadian rhythm in pregnant mice also resulted in delayed enamel development in their babies. Treatment with melatonin receptor antagonist 4P-PDOT in pregnant mice caused underexpression of MTs and AMELX associated with long-lasting deficiency in baby enamel tissue. Electromicroscopic evidence demonstrated increased necrosis and poor enamel mineralization in ameloblasts. The above results suggest that circadian rhythm is important for normal enamel development at both pre- and postnatal stages. Melatonin receptors were partly responsible for the regulation. |
format | Online Article Text |
id | pubmed-4975438 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-49754382016-08-25 Circadian Rhythm Regulates Development of Enamel in Mouse Mandibular First Molar Tao, Jiang Zhai, Yue Park, Hyun Han, Junli Dong, Jianhui Xie, Ming Gu, Ting Lewi, Keidren Ji, Fang Jia, William PLoS One Research Article Rhythmic incremental growth lines and the presence of melatonin receptors were discovered in tooth enamel, suggesting possible role of circadian rhythm. We therefore hypothesized that circadian rhythm may regulate enamel formation through melatonin receptors. To test this hypothesis, we examined expression of melatonin receptors (MTs) and amelogenin (AMELX), a maker of enamel formation, during tooth germ development in mouse. Using qRT-PCR and immunocytochemistry, we found that mRNA and protein levels of both MTs and AMELX in normal mandibular first molar tooth germs increased gradually after birth, peaked at 3 or 4 day postnatal, and then decreased. Expression of MTs and AMELX by immunocytochemistry was significantly delayed in neonatal mice raised in all-dark or all-light environment as well as the enamel development. Furthermore, development of tooth enamel was also delayed showing significant immature histology in those animals, especially for newborn mice raised in all daylight condition. Interestingly, disruption in circadian rhythm in pregnant mice also resulted in delayed enamel development in their babies. Treatment with melatonin receptor antagonist 4P-PDOT in pregnant mice caused underexpression of MTs and AMELX associated with long-lasting deficiency in baby enamel tissue. Electromicroscopic evidence demonstrated increased necrosis and poor enamel mineralization in ameloblasts. The above results suggest that circadian rhythm is important for normal enamel development at both pre- and postnatal stages. Melatonin receptors were partly responsible for the regulation. Public Library of Science 2016-08-05 /pmc/articles/PMC4975438/ /pubmed/27494172 http://dx.doi.org/10.1371/journal.pone.0159946 Text en © 2016 Tao et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Tao, Jiang Zhai, Yue Park, Hyun Han, Junli Dong, Jianhui Xie, Ming Gu, Ting Lewi, Keidren Ji, Fang Jia, William Circadian Rhythm Regulates Development of Enamel in Mouse Mandibular First Molar |
title | Circadian Rhythm Regulates Development of Enamel in Mouse Mandibular First Molar |
title_full | Circadian Rhythm Regulates Development of Enamel in Mouse Mandibular First Molar |
title_fullStr | Circadian Rhythm Regulates Development of Enamel in Mouse Mandibular First Molar |
title_full_unstemmed | Circadian Rhythm Regulates Development of Enamel in Mouse Mandibular First Molar |
title_short | Circadian Rhythm Regulates Development of Enamel in Mouse Mandibular First Molar |
title_sort | circadian rhythm regulates development of enamel in mouse mandibular first molar |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4975438/ https://www.ncbi.nlm.nih.gov/pubmed/27494172 http://dx.doi.org/10.1371/journal.pone.0159946 |
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