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LRP6 acts as a scaffold protein in cardiac gap junction assembly
Low-density lipoprotein receptor-related protein 6 (LRP6) is a Wnt co-receptor in the canonical Wnt/β-catenin signalling. Here, we report the scaffold function of LRP6 in gap junction formation of cardiomyocytes. Cardiac LRP6 is spatially restricted to intercalated discs and binds to gap junction pr...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4895718/ https://www.ncbi.nlm.nih.gov/pubmed/27250245 http://dx.doi.org/10.1038/ncomms11775 |
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author | Li, Jun Li, Changming Liang, Dandan Lv, Fei Yuan, Tianyou The, Erlinda Ma, Xiue Wu, Yahan Zhen, Lixiao Xie, Duanyang Wang, Shiyi Liu, Yuan Huang, Jian Shi, Jingyi Liu, Yi Shi, Dan Xu, Liang Lin, Li Peng, Luying Cui, Jianmin Zhu, Weidong Chen, Yi-Han |
author_facet | Li, Jun Li, Changming Liang, Dandan Lv, Fei Yuan, Tianyou The, Erlinda Ma, Xiue Wu, Yahan Zhen, Lixiao Xie, Duanyang Wang, Shiyi Liu, Yuan Huang, Jian Shi, Jingyi Liu, Yi Shi, Dan Xu, Liang Lin, Li Peng, Luying Cui, Jianmin Zhu, Weidong Chen, Yi-Han |
author_sort | Li, Jun |
collection | PubMed |
description | Low-density lipoprotein receptor-related protein 6 (LRP6) is a Wnt co-receptor in the canonical Wnt/β-catenin signalling. Here, we report the scaffold function of LRP6 in gap junction formation of cardiomyocytes. Cardiac LRP6 is spatially restricted to intercalated discs and binds to gap junction protein connexin 43 (Cx43). A deficiency in LRP6 disrupts Cx43 gap junction formation and thereby impairs the cell-to-cell coupling, which is independent of Wnt/β-catenin signalling. The defect in Cx43 gap junction resulting from LRP6 reduction is attributable to the defective traffic of de novo Cx43 proteins from the endoplasmic reticulum to the Golgi apparatus, leading to the lysosomal degradation of Cx43 proteins. Accordingly, the hearts of conditional cardiac-specific Lrp6-knockout mice consistently exhibit overt reduction of Cx43 gap junction plaques without any abnormality in Wnt signalling and are predisposed to lethal arrhythmias. These findings uncover a distinct role of LRP6 as a platform for intracellular protein trafficking. |
format | Online Article Text |
id | pubmed-4895718 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48957182016-08-18 LRP6 acts as a scaffold protein in cardiac gap junction assembly Li, Jun Li, Changming Liang, Dandan Lv, Fei Yuan, Tianyou The, Erlinda Ma, Xiue Wu, Yahan Zhen, Lixiao Xie, Duanyang Wang, Shiyi Liu, Yuan Huang, Jian Shi, Jingyi Liu, Yi Shi, Dan Xu, Liang Lin, Li Peng, Luying Cui, Jianmin Zhu, Weidong Chen, Yi-Han Nat Commun Article Low-density lipoprotein receptor-related protein 6 (LRP6) is a Wnt co-receptor in the canonical Wnt/β-catenin signalling. Here, we report the scaffold function of LRP6 in gap junction formation of cardiomyocytes. Cardiac LRP6 is spatially restricted to intercalated discs and binds to gap junction protein connexin 43 (Cx43). A deficiency in LRP6 disrupts Cx43 gap junction formation and thereby impairs the cell-to-cell coupling, which is independent of Wnt/β-catenin signalling. The defect in Cx43 gap junction resulting from LRP6 reduction is attributable to the defective traffic of de novo Cx43 proteins from the endoplasmic reticulum to the Golgi apparatus, leading to the lysosomal degradation of Cx43 proteins. Accordingly, the hearts of conditional cardiac-specific Lrp6-knockout mice consistently exhibit overt reduction of Cx43 gap junction plaques without any abnormality in Wnt signalling and are predisposed to lethal arrhythmias. These findings uncover a distinct role of LRP6 as a platform for intracellular protein trafficking. Nature Publishing Group 2016-06-02 /pmc/articles/PMC4895718/ /pubmed/27250245 http://dx.doi.org/10.1038/ncomms11775 Text en Copyright © 2016, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Li, Jun Li, Changming Liang, Dandan Lv, Fei Yuan, Tianyou The, Erlinda Ma, Xiue Wu, Yahan Zhen, Lixiao Xie, Duanyang Wang, Shiyi Liu, Yuan Huang, Jian Shi, Jingyi Liu, Yi Shi, Dan Xu, Liang Lin, Li Peng, Luying Cui, Jianmin Zhu, Weidong Chen, Yi-Han LRP6 acts as a scaffold protein in cardiac gap junction assembly |
title | LRP6 acts as a scaffold protein in cardiac gap junction assembly |
title_full | LRP6 acts as a scaffold protein in cardiac gap junction assembly |
title_fullStr | LRP6 acts as a scaffold protein in cardiac gap junction assembly |
title_full_unstemmed | LRP6 acts as a scaffold protein in cardiac gap junction assembly |
title_short | LRP6 acts as a scaffold protein in cardiac gap junction assembly |
title_sort | lrp6 acts as a scaffold protein in cardiac gap junction assembly |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4895718/ https://www.ncbi.nlm.nih.gov/pubmed/27250245 http://dx.doi.org/10.1038/ncomms11775 |
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