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Cells of the adult human heart
Cardiovascular disease is the leading cause of death worldwide. Advanced insights into disease mechanisms and therapeutic strategies require a deeper understanding of the molecular processes involved in the healthy heart. Knowledge of the full repertoire of cardiac cells and their gene expression pr...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7681775/ https://www.ncbi.nlm.nih.gov/pubmed/32971526 http://dx.doi.org/10.1038/s41586-020-2797-4 |
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author | Litviňuková, Monika Talavera-López, Carlos Maatz, Henrike Reichart, Daniel Worth, Catherine L. Lindberg, Eric L. Kanda, Masatoshi Polanski, Krzysztof Heinig, Matthias Lee, Michael Nadelmann, Emily R. Roberts, Kenny Tuck, Liz Fasouli, Eirini S. DeLaughter, Daniel M. McDonough, Barbara Wakimoto, Hiroko Gorham, Joshua M. Samari, Sara Mahbubani, Krishnaa T. Saeb-Parsy, Kourosh Patone, Giannino Boyle, Joseph J. Zhang, Hongbo Zhang, Hao Viveiros, Anissa Oudit, Gavin Y. Bayraktar, Omer Ali Seidman, J. G. Seidman, Christine E. Noseda, Michela Hubner, Norbert Teichmann, Sarah A. |
author_facet | Litviňuková, Monika Talavera-López, Carlos Maatz, Henrike Reichart, Daniel Worth, Catherine L. Lindberg, Eric L. Kanda, Masatoshi Polanski, Krzysztof Heinig, Matthias Lee, Michael Nadelmann, Emily R. Roberts, Kenny Tuck, Liz Fasouli, Eirini S. DeLaughter, Daniel M. McDonough, Barbara Wakimoto, Hiroko Gorham, Joshua M. Samari, Sara Mahbubani, Krishnaa T. Saeb-Parsy, Kourosh Patone, Giannino Boyle, Joseph J. Zhang, Hongbo Zhang, Hao Viveiros, Anissa Oudit, Gavin Y. Bayraktar, Omer Ali Seidman, J. G. Seidman, Christine E. Noseda, Michela Hubner, Norbert Teichmann, Sarah A. |
author_sort | Litviňuková, Monika |
collection | PubMed |
description | Cardiovascular disease is the leading cause of death worldwide. Advanced insights into disease mechanisms and therapeutic strategies require a deeper understanding of the molecular processes involved in the healthy heart. Knowledge of the full repertoire of cardiac cells and their gene expression profiles is a fundamental first step in this endeavour. Here, using state-of-the-art analyses of large-scale single-cell and single-nucleus transcriptomes, we characterize six anatomical adult heart regions. Our results highlight the cellular heterogeneity of cardiomyocytes, pericytes and fibroblasts, and reveal distinct atrial and ventricular subsets of cells with diverse developmental origins and specialized properties. We define the complexity of the cardiac vasculature and its changes along the arterio-venous axis. In the immune compartment, we identify cardiac-resident macrophages with inflammatory and protective transcriptional signatures. Furthermore, analyses of cell-to-cell interactions highlight different networks of macrophages, fibroblasts and cardiomyocytes between atria and ventricles that are distinct from those of skeletal muscle. Our human cardiac cell atlas improves our understanding of the human heart and provides a valuable reference for future studies. |
format | Online Article Text |
id | pubmed-7681775 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-76817752020-11-23 Cells of the adult human heart Litviňuková, Monika Talavera-López, Carlos Maatz, Henrike Reichart, Daniel Worth, Catherine L. Lindberg, Eric L. Kanda, Masatoshi Polanski, Krzysztof Heinig, Matthias Lee, Michael Nadelmann, Emily R. Roberts, Kenny Tuck, Liz Fasouli, Eirini S. DeLaughter, Daniel M. McDonough, Barbara Wakimoto, Hiroko Gorham, Joshua M. Samari, Sara Mahbubani, Krishnaa T. Saeb-Parsy, Kourosh Patone, Giannino Boyle, Joseph J. Zhang, Hongbo Zhang, Hao Viveiros, Anissa Oudit, Gavin Y. Bayraktar, Omer Ali Seidman, J. G. Seidman, Christine E. Noseda, Michela Hubner, Norbert Teichmann, Sarah A. Nature Article Cardiovascular disease is the leading cause of death worldwide. Advanced insights into disease mechanisms and therapeutic strategies require a deeper understanding of the molecular processes involved in the healthy heart. Knowledge of the full repertoire of cardiac cells and their gene expression profiles is a fundamental first step in this endeavour. Here, using state-of-the-art analyses of large-scale single-cell and single-nucleus transcriptomes, we characterize six anatomical adult heart regions. Our results highlight the cellular heterogeneity of cardiomyocytes, pericytes and fibroblasts, and reveal distinct atrial and ventricular subsets of cells with diverse developmental origins and specialized properties. We define the complexity of the cardiac vasculature and its changes along the arterio-venous axis. In the immune compartment, we identify cardiac-resident macrophages with inflammatory and protective transcriptional signatures. Furthermore, analyses of cell-to-cell interactions highlight different networks of macrophages, fibroblasts and cardiomyocytes between atria and ventricles that are distinct from those of skeletal muscle. Our human cardiac cell atlas improves our understanding of the human heart and provides a valuable reference for future studies. Nature Publishing Group UK 2020-09-24 2020 /pmc/articles/PMC7681775/ /pubmed/32971526 http://dx.doi.org/10.1038/s41586-020-2797-4 Text en © The Author(s) 2020 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 Litviňuková, Monika Talavera-López, Carlos Maatz, Henrike Reichart, Daniel Worth, Catherine L. Lindberg, Eric L. Kanda, Masatoshi Polanski, Krzysztof Heinig, Matthias Lee, Michael Nadelmann, Emily R. Roberts, Kenny Tuck, Liz Fasouli, Eirini S. DeLaughter, Daniel M. McDonough, Barbara Wakimoto, Hiroko Gorham, Joshua M. Samari, Sara Mahbubani, Krishnaa T. Saeb-Parsy, Kourosh Patone, Giannino Boyle, Joseph J. Zhang, Hongbo Zhang, Hao Viveiros, Anissa Oudit, Gavin Y. Bayraktar, Omer Ali Seidman, J. G. Seidman, Christine E. Noseda, Michela Hubner, Norbert Teichmann, Sarah A. Cells of the adult human heart |
title | Cells of the adult human heart |
title_full | Cells of the adult human heart |
title_fullStr | Cells of the adult human heart |
title_full_unstemmed | Cells of the adult human heart |
title_short | Cells of the adult human heart |
title_sort | cells of the adult human heart |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7681775/ https://www.ncbi.nlm.nih.gov/pubmed/32971526 http://dx.doi.org/10.1038/s41586-020-2797-4 |
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