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Homogeneous 2D and 3D alignment of cardiomyocyte in dilated cardiomyopathy revealed by intravital heart imaging
In contrast to hypertrophic cardiomyopathy, there has been reported no specific pattern of cardiomyocyte array in dilated cardiomyopathy (DCM), partially because lack of alignment assessment in a three-dimensional (3D) manner. Here we have established a novel method to evaluate cardiomyocyte alignme...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8289833/ https://www.ncbi.nlm.nih.gov/pubmed/34282197 http://dx.doi.org/10.1038/s41598-021-94100-z |
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author | Masuyama, Kiyoshi Higo, Tomoaki Lee, Jong-Kook Matsuura, Ryohei Jones, Ian Bakal, Chris Higo, Shuichiro Morimoto, Sachio Miyagawa, Shigeru Sawa, Yoshiki Sakata, Yasushi |
author_facet | Masuyama, Kiyoshi Higo, Tomoaki Lee, Jong-Kook Matsuura, Ryohei Jones, Ian Bakal, Chris Higo, Shuichiro Morimoto, Sachio Miyagawa, Shigeru Sawa, Yoshiki Sakata, Yasushi |
author_sort | Masuyama, Kiyoshi |
collection | PubMed |
description | In contrast to hypertrophic cardiomyopathy, there has been reported no specific pattern of cardiomyocyte array in dilated cardiomyopathy (DCM), partially because lack of alignment assessment in a three-dimensional (3D) manner. Here we have established a novel method to evaluate cardiomyocyte alignment in 3D using intravital heart imaging and demonstrated homogeneous alignment in DCM mice. Whilst cardiomyocytes of control mice changed their alignment by every layer in 3D and position twistedly even in a single layer, termed myocyte twist, cardiomyocytes of DCM mice aligned homogeneously both in two-dimensional (2D) and in 3D and lost myocyte twist. Manipulation of cultured cardiomyocyte toward homogeneously aligned increased their contractility, suggesting that homogeneous alignment in DCM mice is due to a sort of alignment remodelling as a way to compensate cardiac dysfunction. Our findings provide the first intravital evidence of cardiomyocyte alignment and will bring new insights into understanding the mechanism of heart failure. |
format | Online Article Text |
id | pubmed-8289833 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-82898332021-07-21 Homogeneous 2D and 3D alignment of cardiomyocyte in dilated cardiomyopathy revealed by intravital heart imaging Masuyama, Kiyoshi Higo, Tomoaki Lee, Jong-Kook Matsuura, Ryohei Jones, Ian Bakal, Chris Higo, Shuichiro Morimoto, Sachio Miyagawa, Shigeru Sawa, Yoshiki Sakata, Yasushi Sci Rep Article In contrast to hypertrophic cardiomyopathy, there has been reported no specific pattern of cardiomyocyte array in dilated cardiomyopathy (DCM), partially because lack of alignment assessment in a three-dimensional (3D) manner. Here we have established a novel method to evaluate cardiomyocyte alignment in 3D using intravital heart imaging and demonstrated homogeneous alignment in DCM mice. Whilst cardiomyocytes of control mice changed their alignment by every layer in 3D and position twistedly even in a single layer, termed myocyte twist, cardiomyocytes of DCM mice aligned homogeneously both in two-dimensional (2D) and in 3D and lost myocyte twist. Manipulation of cultured cardiomyocyte toward homogeneously aligned increased their contractility, suggesting that homogeneous alignment in DCM mice is due to a sort of alignment remodelling as a way to compensate cardiac dysfunction. Our findings provide the first intravital evidence of cardiomyocyte alignment and will bring new insights into understanding the mechanism of heart failure. Nature Publishing Group UK 2021-07-19 /pmc/articles/PMC8289833/ /pubmed/34282197 http://dx.doi.org/10.1038/s41598-021-94100-z Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Masuyama, Kiyoshi Higo, Tomoaki Lee, Jong-Kook Matsuura, Ryohei Jones, Ian Bakal, Chris Higo, Shuichiro Morimoto, Sachio Miyagawa, Shigeru Sawa, Yoshiki Sakata, Yasushi Homogeneous 2D and 3D alignment of cardiomyocyte in dilated cardiomyopathy revealed by intravital heart imaging |
title | Homogeneous 2D and 3D alignment of cardiomyocyte in dilated cardiomyopathy revealed by intravital heart imaging |
title_full | Homogeneous 2D and 3D alignment of cardiomyocyte in dilated cardiomyopathy revealed by intravital heart imaging |
title_fullStr | Homogeneous 2D and 3D alignment of cardiomyocyte in dilated cardiomyopathy revealed by intravital heart imaging |
title_full_unstemmed | Homogeneous 2D and 3D alignment of cardiomyocyte in dilated cardiomyopathy revealed by intravital heart imaging |
title_short | Homogeneous 2D and 3D alignment of cardiomyocyte in dilated cardiomyopathy revealed by intravital heart imaging |
title_sort | homogeneous 2d and 3d alignment of cardiomyocyte in dilated cardiomyopathy revealed by intravital heart imaging |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8289833/ https://www.ncbi.nlm.nih.gov/pubmed/34282197 http://dx.doi.org/10.1038/s41598-021-94100-z |
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