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Roles of monocarboxylate transporter subtypes in promotion and suppression of osteoclast differentiation and survival on bone
Monocarboxylate transporters (MCTs) provide transmembrane transport of monocarboxylates such as lactate and pyruvate. The present results showed that α-cyano-4-hydroxycinnamic acid (CHC), an inhibitor of MCTs, promoted osteoclast differentiation from macrophages at lower concentrations (0.1–0.3 mM)...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6821745/ https://www.ncbi.nlm.nih.gov/pubmed/31666601 http://dx.doi.org/10.1038/s41598-019-52128-2 |
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author | Imai, Hiroko Yoshimura, Kentaro Miyamoto, Yoichi Sasa, Kiyohito Sugano, Marika Chatani, Masahiro Takami, Masamichi Yamamoto, Matsuo Kamijo, Ryutaro |
author_facet | Imai, Hiroko Yoshimura, Kentaro Miyamoto, Yoichi Sasa, Kiyohito Sugano, Marika Chatani, Masahiro Takami, Masamichi Yamamoto, Matsuo Kamijo, Ryutaro |
author_sort | Imai, Hiroko |
collection | PubMed |
description | Monocarboxylate transporters (MCTs) provide transmembrane transport of monocarboxylates such as lactate and pyruvate. The present results showed that α-cyano-4-hydroxycinnamic acid (CHC), an inhibitor of MCTs, promoted osteoclast differentiation from macrophages at lower concentrations (0.1–0.3 mM) and suppressed that at a higher concentration (1.0 mM). On the other hand, CHC reduced the number of mature osteoclasts on the surface of dentin in a concentration-dependent manner. Additionally, macrophages and osteoclasts were found to express the Mct1, Mct2, and Mct4 genes, with Mct1 and Mct4 expression higher in macrophages, and that of Mct2 higher in osteoclasts. Although Mct1 gene knockdown in macrophages enhanced osteoclast formation induced by RANKL, Mct2 gene knockdown suppressed that. Finally, Mct2 gene silencing in mature osteoclasts decreased their number and, thereby, bone resorption. These results suggest that MCT1 is a negative regulator and MCT2 a positive regulator of osteoclast differentiation, while MCT2 is required for bone resorption by osteoclasts. |
format | Online Article Text |
id | pubmed-6821745 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-68217452019-11-05 Roles of monocarboxylate transporter subtypes in promotion and suppression of osteoclast differentiation and survival on bone Imai, Hiroko Yoshimura, Kentaro Miyamoto, Yoichi Sasa, Kiyohito Sugano, Marika Chatani, Masahiro Takami, Masamichi Yamamoto, Matsuo Kamijo, Ryutaro Sci Rep Article Monocarboxylate transporters (MCTs) provide transmembrane transport of monocarboxylates such as lactate and pyruvate. The present results showed that α-cyano-4-hydroxycinnamic acid (CHC), an inhibitor of MCTs, promoted osteoclast differentiation from macrophages at lower concentrations (0.1–0.3 mM) and suppressed that at a higher concentration (1.0 mM). On the other hand, CHC reduced the number of mature osteoclasts on the surface of dentin in a concentration-dependent manner. Additionally, macrophages and osteoclasts were found to express the Mct1, Mct2, and Mct4 genes, with Mct1 and Mct4 expression higher in macrophages, and that of Mct2 higher in osteoclasts. Although Mct1 gene knockdown in macrophages enhanced osteoclast formation induced by RANKL, Mct2 gene knockdown suppressed that. Finally, Mct2 gene silencing in mature osteoclasts decreased their number and, thereby, bone resorption. These results suggest that MCT1 is a negative regulator and MCT2 a positive regulator of osteoclast differentiation, while MCT2 is required for bone resorption by osteoclasts. Nature Publishing Group UK 2019-10-30 /pmc/articles/PMC6821745/ /pubmed/31666601 http://dx.doi.org/10.1038/s41598-019-52128-2 Text en © The Author(s) 2019 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 Imai, Hiroko Yoshimura, Kentaro Miyamoto, Yoichi Sasa, Kiyohito Sugano, Marika Chatani, Masahiro Takami, Masamichi Yamamoto, Matsuo Kamijo, Ryutaro Roles of monocarboxylate transporter subtypes in promotion and suppression of osteoclast differentiation and survival on bone |
title | Roles of monocarboxylate transporter subtypes in promotion and suppression of osteoclast differentiation and survival on bone |
title_full | Roles of monocarboxylate transporter subtypes in promotion and suppression of osteoclast differentiation and survival on bone |
title_fullStr | Roles of monocarboxylate transporter subtypes in promotion and suppression of osteoclast differentiation and survival on bone |
title_full_unstemmed | Roles of monocarboxylate transporter subtypes in promotion and suppression of osteoclast differentiation and survival on bone |
title_short | Roles of monocarboxylate transporter subtypes in promotion and suppression of osteoclast differentiation and survival on bone |
title_sort | roles of monocarboxylate transporter subtypes in promotion and suppression of osteoclast differentiation and survival on bone |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6821745/ https://www.ncbi.nlm.nih.gov/pubmed/31666601 http://dx.doi.org/10.1038/s41598-019-52128-2 |
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