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The Role of Ca(2+)-NFATc1 Signaling and Its Modulation on Osteoclastogenesis

The increasing of intracellular calcium concentration is a fundamental process for mediating osteoclastogenesis, which is involved in osteoclastic bone resorption. Cytosolic calcium binds to calmodulin and subsequently activates calcineurin, leading to NFATc1 activation, a master transcription facto...

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Detalles Bibliográficos
Autores principales: Kang, Jung Yun, Kang, Namju, Yang, Yu-Mi, Hong, Jeong Hee, Shin, Dong Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7279283/
https://www.ncbi.nlm.nih.gov/pubmed/32455661
http://dx.doi.org/10.3390/ijms21103646
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author Kang, Jung Yun
Kang, Namju
Yang, Yu-Mi
Hong, Jeong Hee
Shin, Dong Min
author_facet Kang, Jung Yun
Kang, Namju
Yang, Yu-Mi
Hong, Jeong Hee
Shin, Dong Min
author_sort Kang, Jung Yun
collection PubMed
description The increasing of intracellular calcium concentration is a fundamental process for mediating osteoclastogenesis, which is involved in osteoclastic bone resorption. Cytosolic calcium binds to calmodulin and subsequently activates calcineurin, leading to NFATc1 activation, a master transcription factor required for osteoclast differentiation. Targeting the various activation processes in osteoclastogenesis provides various therapeutic strategies for bone loss. Diverse compounds that modulate calcium signaling have been applied to regulate osteoclast differentiation and, subsequently, attenuate bone loss. Thus, in this review, we summarized the modulation of the NFATc1 pathway through various compounds that regulate calcium signaling and the calcium influx machinery. Furthermore, we addressed the involvement of transient receptor potential channels in osteoclastogenesis.
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spelling pubmed-72792832020-06-15 The Role of Ca(2+)-NFATc1 Signaling and Its Modulation on Osteoclastogenesis Kang, Jung Yun Kang, Namju Yang, Yu-Mi Hong, Jeong Hee Shin, Dong Min Int J Mol Sci Review The increasing of intracellular calcium concentration is a fundamental process for mediating osteoclastogenesis, which is involved in osteoclastic bone resorption. Cytosolic calcium binds to calmodulin and subsequently activates calcineurin, leading to NFATc1 activation, a master transcription factor required for osteoclast differentiation. Targeting the various activation processes in osteoclastogenesis provides various therapeutic strategies for bone loss. Diverse compounds that modulate calcium signaling have been applied to regulate osteoclast differentiation and, subsequently, attenuate bone loss. Thus, in this review, we summarized the modulation of the NFATc1 pathway through various compounds that regulate calcium signaling and the calcium influx machinery. Furthermore, we addressed the involvement of transient receptor potential channels in osteoclastogenesis. MDPI 2020-05-21 /pmc/articles/PMC7279283/ /pubmed/32455661 http://dx.doi.org/10.3390/ijms21103646 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Kang, Jung Yun
Kang, Namju
Yang, Yu-Mi
Hong, Jeong Hee
Shin, Dong Min
The Role of Ca(2+)-NFATc1 Signaling and Its Modulation on Osteoclastogenesis
title The Role of Ca(2+)-NFATc1 Signaling and Its Modulation on Osteoclastogenesis
title_full The Role of Ca(2+)-NFATc1 Signaling and Its Modulation on Osteoclastogenesis
title_fullStr The Role of Ca(2+)-NFATc1 Signaling and Its Modulation on Osteoclastogenesis
title_full_unstemmed The Role of Ca(2+)-NFATc1 Signaling and Its Modulation on Osteoclastogenesis
title_short The Role of Ca(2+)-NFATc1 Signaling and Its Modulation on Osteoclastogenesis
title_sort role of ca(2+)-nfatc1 signaling and its modulation on osteoclastogenesis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7279283/
https://www.ncbi.nlm.nih.gov/pubmed/32455661
http://dx.doi.org/10.3390/ijms21103646
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