Cargando…

Altered intercellular communication and extracellular matrix signaling as a potential disease mechanism in human hypertrophic cardiomyopathy

Hypertrophic cardiomyopathy (HCM) is considered a primary disorder of the sarcomere resulting in unexplained left ventricular hypertrophy but the paradoxical association of nonmyocyte phenotypes such as fibrosis, mitral valve anomalies and microvascular occlusion is unexplained. To understand the in...

Descripción completa

Detalles Bibliográficos
Autores principales: Larson, Amy, Codden, Christina J., Huggins, Gordon S., Rastegar, Hassan, Chen, Frederick Y., Maron, Barry J., Rowin, Ethan J., Maron, Martin S., Chin, Michael T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8956620/
https://www.ncbi.nlm.nih.gov/pubmed/35338173
http://dx.doi.org/10.1038/s41598-022-08561-x
_version_ 1784676603996930048
author Larson, Amy
Codden, Christina J.
Huggins, Gordon S.
Rastegar, Hassan
Chen, Frederick Y.
Maron, Barry J.
Rowin, Ethan J.
Maron, Martin S.
Chin, Michael T.
author_facet Larson, Amy
Codden, Christina J.
Huggins, Gordon S.
Rastegar, Hassan
Chen, Frederick Y.
Maron, Barry J.
Rowin, Ethan J.
Maron, Martin S.
Chin, Michael T.
author_sort Larson, Amy
collection PubMed
description Hypertrophic cardiomyopathy (HCM) is considered a primary disorder of the sarcomere resulting in unexplained left ventricular hypertrophy but the paradoxical association of nonmyocyte phenotypes such as fibrosis, mitral valve anomalies and microvascular occlusion is unexplained. To understand the interplay between cardiomyocyte and nonmyocyte cell types in human HCM, single nuclei RNA-sequencing was performed on myectomy specimens from HCM patients with left ventricular outflow tract obstruction and control samples from donor hearts free of cardiovascular disease. Clustering analysis based on gene expression patterns identified a total of 34 distinct cell populations, which were classified into 10 different cell types based on marker gene expression. Differential gene expression analysis comparing HCM to Normal datasets revealed differences in sarcomere and extracellular matrix gene expression. Analysis of expressed ligand-receptor pairs across multiple cell types indicated profound alteration in HCM intercellular communication, particularly between cardiomyocytes and fibroblasts, fibroblasts and lymphocytes and involving integrin β1 and its multiple extracellular matrix (ECM) cognate ligands. These findings provide a paradigm for how sarcomere dysfunction is associated with reduced cardiomyocyte secretion of ECM ligands, altered fibroblast ligand-receptor interactions with other cell types and increased fibroblast to lymphocyte signaling, which can further alter the ECM composition and promote nonmyocyte phenotypes.
format Online
Article
Text
id pubmed-8956620
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-89566202022-03-28 Altered intercellular communication and extracellular matrix signaling as a potential disease mechanism in human hypertrophic cardiomyopathy Larson, Amy Codden, Christina J. Huggins, Gordon S. Rastegar, Hassan Chen, Frederick Y. Maron, Barry J. Rowin, Ethan J. Maron, Martin S. Chin, Michael T. Sci Rep Article Hypertrophic cardiomyopathy (HCM) is considered a primary disorder of the sarcomere resulting in unexplained left ventricular hypertrophy but the paradoxical association of nonmyocyte phenotypes such as fibrosis, mitral valve anomalies and microvascular occlusion is unexplained. To understand the interplay between cardiomyocyte and nonmyocyte cell types in human HCM, single nuclei RNA-sequencing was performed on myectomy specimens from HCM patients with left ventricular outflow tract obstruction and control samples from donor hearts free of cardiovascular disease. Clustering analysis based on gene expression patterns identified a total of 34 distinct cell populations, which were classified into 10 different cell types based on marker gene expression. Differential gene expression analysis comparing HCM to Normal datasets revealed differences in sarcomere and extracellular matrix gene expression. Analysis of expressed ligand-receptor pairs across multiple cell types indicated profound alteration in HCM intercellular communication, particularly between cardiomyocytes and fibroblasts, fibroblasts and lymphocytes and involving integrin β1 and its multiple extracellular matrix (ECM) cognate ligands. These findings provide a paradigm for how sarcomere dysfunction is associated with reduced cardiomyocyte secretion of ECM ligands, altered fibroblast ligand-receptor interactions with other cell types and increased fibroblast to lymphocyte signaling, which can further alter the ECM composition and promote nonmyocyte phenotypes. Nature Publishing Group UK 2022-03-25 /pmc/articles/PMC8956620/ /pubmed/35338173 http://dx.doi.org/10.1038/s41598-022-08561-x Text en © The Author(s) 2022 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
Larson, Amy
Codden, Christina J.
Huggins, Gordon S.
Rastegar, Hassan
Chen, Frederick Y.
Maron, Barry J.
Rowin, Ethan J.
Maron, Martin S.
Chin, Michael T.
Altered intercellular communication and extracellular matrix signaling as a potential disease mechanism in human hypertrophic cardiomyopathy
title Altered intercellular communication and extracellular matrix signaling as a potential disease mechanism in human hypertrophic cardiomyopathy
title_full Altered intercellular communication and extracellular matrix signaling as a potential disease mechanism in human hypertrophic cardiomyopathy
title_fullStr Altered intercellular communication and extracellular matrix signaling as a potential disease mechanism in human hypertrophic cardiomyopathy
title_full_unstemmed Altered intercellular communication and extracellular matrix signaling as a potential disease mechanism in human hypertrophic cardiomyopathy
title_short Altered intercellular communication and extracellular matrix signaling as a potential disease mechanism in human hypertrophic cardiomyopathy
title_sort altered intercellular communication and extracellular matrix signaling as a potential disease mechanism in human hypertrophic cardiomyopathy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8956620/
https://www.ncbi.nlm.nih.gov/pubmed/35338173
http://dx.doi.org/10.1038/s41598-022-08561-x
work_keys_str_mv AT larsonamy alteredintercellularcommunicationandextracellularmatrixsignalingasapotentialdiseasemechanisminhumanhypertrophiccardiomyopathy
AT coddenchristinaj alteredintercellularcommunicationandextracellularmatrixsignalingasapotentialdiseasemechanisminhumanhypertrophiccardiomyopathy
AT hugginsgordons alteredintercellularcommunicationandextracellularmatrixsignalingasapotentialdiseasemechanisminhumanhypertrophiccardiomyopathy
AT rastegarhassan alteredintercellularcommunicationandextracellularmatrixsignalingasapotentialdiseasemechanisminhumanhypertrophiccardiomyopathy
AT chenfredericky alteredintercellularcommunicationandextracellularmatrixsignalingasapotentialdiseasemechanisminhumanhypertrophiccardiomyopathy
AT maronbarryj alteredintercellularcommunicationandextracellularmatrixsignalingasapotentialdiseasemechanisminhumanhypertrophiccardiomyopathy
AT rowinethanj alteredintercellularcommunicationandextracellularmatrixsignalingasapotentialdiseasemechanisminhumanhypertrophiccardiomyopathy
AT maronmartins alteredintercellularcommunicationandextracellularmatrixsignalingasapotentialdiseasemechanisminhumanhypertrophiccardiomyopathy
AT chinmichaelt alteredintercellularcommunicationandextracellularmatrixsignalingasapotentialdiseasemechanisminhumanhypertrophiccardiomyopathy