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TMCO1-mediated Ca(2+) leak underlies osteoblast functions via CaMKII signaling

Transmembrane and coiled-coil domains 1 (TMCO1) is a recently identified Ca(2+) leak channel in the endoplasmic reticulum. TMCO1 dysfunction in humans is associated with dysmorphism, mental retardation, glaucoma and the occurrence of cancer. Here we show an essential role of TMCO1 in osteogenesis me...

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Autores principales: Li, Jianwei, Liu, Caizhi, Li, Yuheng, Zheng, Qiaoxia, Xu, Youjia, Liu, Beibei, Sun, Weijia, Li, Yuan, Ji, Shuhui, Liu, Mingwei, Zhang, Jing, Zhao, Dingsheng, Du, Ruikai, Liu, Zizhong, Zhong, Guohui, Sun, Cuiwei, Wang, Yanqing, Song, Jinping, Zhang, Shu, Qin, Jun, Ling, Shukuan, Wang, Xianhua, Li, Yingxian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6453895/
https://www.ncbi.nlm.nih.gov/pubmed/30962442
http://dx.doi.org/10.1038/s41467-019-09653-5
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author Li, Jianwei
Liu, Caizhi
Li, Yuheng
Zheng, Qiaoxia
Xu, Youjia
Liu, Beibei
Sun, Weijia
Li, Yuan
Ji, Shuhui
Liu, Mingwei
Zhang, Jing
Zhao, Dingsheng
Du, Ruikai
Liu, Zizhong
Zhong, Guohui
Sun, Cuiwei
Wang, Yanqing
Song, Jinping
Zhang, Shu
Qin, Jun
Ling, Shukuan
Wang, Xianhua
Li, Yingxian
author_facet Li, Jianwei
Liu, Caizhi
Li, Yuheng
Zheng, Qiaoxia
Xu, Youjia
Liu, Beibei
Sun, Weijia
Li, Yuan
Ji, Shuhui
Liu, Mingwei
Zhang, Jing
Zhao, Dingsheng
Du, Ruikai
Liu, Zizhong
Zhong, Guohui
Sun, Cuiwei
Wang, Yanqing
Song, Jinping
Zhang, Shu
Qin, Jun
Ling, Shukuan
Wang, Xianhua
Li, Yingxian
author_sort Li, Jianwei
collection PubMed
description Transmembrane and coiled-coil domains 1 (TMCO1) is a recently identified Ca(2+) leak channel in the endoplasmic reticulum. TMCO1 dysfunction in humans is associated with dysmorphism, mental retardation, glaucoma and the occurrence of cancer. Here we show an essential role of TMCO1 in osteogenesis mediated by local Ca(2+)/CaMKII signaling in osteoblasts. TMCO1 levels were significantly decreased in bone from both osteoporosis patients and bone-loss mouse models. Tmco1(−/−) mice exhibited loss of bone mass and altered microarchitecture characteristic of osteoporosis. In the absence of TMCO1, decreased HDAC4 phosphorylation resulted in nuclear enrichment of HADC4, which leads to deacetylation and degradation of RUNX2, the master regulator of osteogenesis. We further demonstrate that TMCO1-mediated Ca(2+) leak provides local Ca(2+) signals to activate the CaMKII-HDAC4-RUNX2 signaling axis. The establishment of TMCO1 as a pivotal player in osteogenesis uncovers a novel potential therapeutic target for ameliorating osteoporosis.
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spelling pubmed-64538952019-04-10 TMCO1-mediated Ca(2+) leak underlies osteoblast functions via CaMKII signaling Li, Jianwei Liu, Caizhi Li, Yuheng Zheng, Qiaoxia Xu, Youjia Liu, Beibei Sun, Weijia Li, Yuan Ji, Shuhui Liu, Mingwei Zhang, Jing Zhao, Dingsheng Du, Ruikai Liu, Zizhong Zhong, Guohui Sun, Cuiwei Wang, Yanqing Song, Jinping Zhang, Shu Qin, Jun Ling, Shukuan Wang, Xianhua Li, Yingxian Nat Commun Article Transmembrane and coiled-coil domains 1 (TMCO1) is a recently identified Ca(2+) leak channel in the endoplasmic reticulum. TMCO1 dysfunction in humans is associated with dysmorphism, mental retardation, glaucoma and the occurrence of cancer. Here we show an essential role of TMCO1 in osteogenesis mediated by local Ca(2+)/CaMKII signaling in osteoblasts. TMCO1 levels were significantly decreased in bone from both osteoporosis patients and bone-loss mouse models. Tmco1(−/−) mice exhibited loss of bone mass and altered microarchitecture characteristic of osteoporosis. In the absence of TMCO1, decreased HDAC4 phosphorylation resulted in nuclear enrichment of HADC4, which leads to deacetylation and degradation of RUNX2, the master regulator of osteogenesis. We further demonstrate that TMCO1-mediated Ca(2+) leak provides local Ca(2+) signals to activate the CaMKII-HDAC4-RUNX2 signaling axis. The establishment of TMCO1 as a pivotal player in osteogenesis uncovers a novel potential therapeutic target for ameliorating osteoporosis. Nature Publishing Group UK 2019-04-08 /pmc/articles/PMC6453895/ /pubmed/30962442 http://dx.doi.org/10.1038/s41467-019-09653-5 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
Li, Jianwei
Liu, Caizhi
Li, Yuheng
Zheng, Qiaoxia
Xu, Youjia
Liu, Beibei
Sun, Weijia
Li, Yuan
Ji, Shuhui
Liu, Mingwei
Zhang, Jing
Zhao, Dingsheng
Du, Ruikai
Liu, Zizhong
Zhong, Guohui
Sun, Cuiwei
Wang, Yanqing
Song, Jinping
Zhang, Shu
Qin, Jun
Ling, Shukuan
Wang, Xianhua
Li, Yingxian
TMCO1-mediated Ca(2+) leak underlies osteoblast functions via CaMKII signaling
title TMCO1-mediated Ca(2+) leak underlies osteoblast functions via CaMKII signaling
title_full TMCO1-mediated Ca(2+) leak underlies osteoblast functions via CaMKII signaling
title_fullStr TMCO1-mediated Ca(2+) leak underlies osteoblast functions via CaMKII signaling
title_full_unstemmed TMCO1-mediated Ca(2+) leak underlies osteoblast functions via CaMKII signaling
title_short TMCO1-mediated Ca(2+) leak underlies osteoblast functions via CaMKII signaling
title_sort tmco1-mediated ca(2+) leak underlies osteoblast functions via camkii signaling
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6453895/
https://www.ncbi.nlm.nih.gov/pubmed/30962442
http://dx.doi.org/10.1038/s41467-019-09653-5
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