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The crucial role of the TRPM7 kinase domain in the early stage of amelogenesis
Transient receptor potential melastatin-7 (TRPM7) is a bi-functional protein containing a kinase domain fused to an ion channel. TRPM7 is highly expressed in ameloblasts during tooth development. Here we show that TRPM7 kinase-inactive knock-in mutant mice (TRPM7 KR mice) exhibited small enamel volu...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5741708/ https://www.ncbi.nlm.nih.gov/pubmed/29273814 http://dx.doi.org/10.1038/s41598-017-18291-0 |
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author | Ogata, Kayoko Tsumuraya, Tomoyuki Oka, Kyoko Shin, Masashi Okamoto, Fujio Kajiya, Hiroshi Katagiri, Chiaki Ozaki, Masao Matsushita, Masayuki Okabe, Koji |
author_facet | Ogata, Kayoko Tsumuraya, Tomoyuki Oka, Kyoko Shin, Masashi Okamoto, Fujio Kajiya, Hiroshi Katagiri, Chiaki Ozaki, Masao Matsushita, Masayuki Okabe, Koji |
author_sort | Ogata, Kayoko |
collection | PubMed |
description | Transient receptor potential melastatin-7 (TRPM7) is a bi-functional protein containing a kinase domain fused to an ion channel. TRPM7 is highly expressed in ameloblasts during tooth development. Here we show that TRPM7 kinase-inactive knock-in mutant mice (TRPM7 KR mice) exhibited small enamel volume with opaque white-colored incisors. The TRPM7 channel function of ameloblast-lineage cells from TRPM7 KR mice was normal. Interestingly, phosphorylation of intracellular molecules including Smad1/5/9, p38 and cAMP response element binding protein (CREB) was inhibited in ameloblasts from TRPM7 KR mice at the pre-secretory stage. An immunoprecipitation assay showed that CREB was bound to TRPM7, suggesting that direct phosphorylation of CREB by TRPM7 was inhibited in ameloblast-lineage cells from TRPM7 KR mice. These results indicate that the function of the TRPM7 kinase domain plays an important role in ameloblast differentiation, independent of TRPM7 channel activity, via phosphorylation of CREB. |
format | Online Article Text |
id | pubmed-5741708 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57417082018-01-03 The crucial role of the TRPM7 kinase domain in the early stage of amelogenesis Ogata, Kayoko Tsumuraya, Tomoyuki Oka, Kyoko Shin, Masashi Okamoto, Fujio Kajiya, Hiroshi Katagiri, Chiaki Ozaki, Masao Matsushita, Masayuki Okabe, Koji Sci Rep Article Transient receptor potential melastatin-7 (TRPM7) is a bi-functional protein containing a kinase domain fused to an ion channel. TRPM7 is highly expressed in ameloblasts during tooth development. Here we show that TRPM7 kinase-inactive knock-in mutant mice (TRPM7 KR mice) exhibited small enamel volume with opaque white-colored incisors. The TRPM7 channel function of ameloblast-lineage cells from TRPM7 KR mice was normal. Interestingly, phosphorylation of intracellular molecules including Smad1/5/9, p38 and cAMP response element binding protein (CREB) was inhibited in ameloblasts from TRPM7 KR mice at the pre-secretory stage. An immunoprecipitation assay showed that CREB was bound to TRPM7, suggesting that direct phosphorylation of CREB by TRPM7 was inhibited in ameloblast-lineage cells from TRPM7 KR mice. These results indicate that the function of the TRPM7 kinase domain plays an important role in ameloblast differentiation, independent of TRPM7 channel activity, via phosphorylation of CREB. Nature Publishing Group UK 2017-12-22 /pmc/articles/PMC5741708/ /pubmed/29273814 http://dx.doi.org/10.1038/s41598-017-18291-0 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Ogata, Kayoko Tsumuraya, Tomoyuki Oka, Kyoko Shin, Masashi Okamoto, Fujio Kajiya, Hiroshi Katagiri, Chiaki Ozaki, Masao Matsushita, Masayuki Okabe, Koji The crucial role of the TRPM7 kinase domain in the early stage of amelogenesis |
title | The crucial role of the TRPM7 kinase domain in the early stage of amelogenesis |
title_full | The crucial role of the TRPM7 kinase domain in the early stage of amelogenesis |
title_fullStr | The crucial role of the TRPM7 kinase domain in the early stage of amelogenesis |
title_full_unstemmed | The crucial role of the TRPM7 kinase domain in the early stage of amelogenesis |
title_short | The crucial role of the TRPM7 kinase domain in the early stage of amelogenesis |
title_sort | crucial role of the trpm7 kinase domain in the early stage of amelogenesis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5741708/ https://www.ncbi.nlm.nih.gov/pubmed/29273814 http://dx.doi.org/10.1038/s41598-017-18291-0 |
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