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CCBE1 Is Essential for Epicardial Function during Myocardium Development
The epicardium is a single cell layer of mesothelial cells that plays a critical role during heart development contributing to different cardiac cell types of the developing heart through epithelial-to-mesenchymal transition (EMT). Moreover, the epicardium is a source of secreted growth factors that...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9604378/ https://www.ncbi.nlm.nih.gov/pubmed/36293499 http://dx.doi.org/10.3390/ijms232012642 |
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author | Bonet, Fernando Añez, Sabrina Brito Inácio, José Manuel Futschik, Matthias E. Belo, José Antonio |
author_facet | Bonet, Fernando Añez, Sabrina Brito Inácio, José Manuel Futschik, Matthias E. Belo, José Antonio |
author_sort | Bonet, Fernando |
collection | PubMed |
description | The epicardium is a single cell layer of mesothelial cells that plays a critical role during heart development contributing to different cardiac cell types of the developing heart through epithelial-to-mesenchymal transition (EMT). Moreover, the epicardium is a source of secreted growth factors that promote myocardial growth. CCBE1 is a secreted extracellular matrix protein expressed by epicardial cells that is required for the formation of the primitive coronary plexus. However, the role of CCBE1 during epicardial development was still unknown. Here, using a Ccbe1 knockout (KO) mouse model, we observed that loss of CCBE1 leads to congenital heart defects including thinner and hyper-trabeculated ventricular myocardium. In addition, Ccbe1 mutant hearts displayed reduced proliferation of cardiomyocyte and epicardial cells. Epicardial outgrowth culture assay to assess epicardial-derived cells (EPDC) migration showed reduced invasion of the collagen gel by EPDCs in Ccbe1 KO epicardial explants. Ccbe1 KO hearts also displayed fewer nonmyocyte/nonendothelial cells intramyocardially with a reduced proliferation rate. Additionally, RNA-seq data and experimental validation by qRT-PCR showed a marked deregulation of EMT-related genes in developing Ccbe1 mutant hearts. Together, these findings indicate that the myocardium defects in Ccbe1 KO mice arise from disruption of epicardial development and function. |
format | Online Article Text |
id | pubmed-9604378 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-96043782022-10-27 CCBE1 Is Essential for Epicardial Function during Myocardium Development Bonet, Fernando Añez, Sabrina Brito Inácio, José Manuel Futschik, Matthias E. Belo, José Antonio Int J Mol Sci Article The epicardium is a single cell layer of mesothelial cells that plays a critical role during heart development contributing to different cardiac cell types of the developing heart through epithelial-to-mesenchymal transition (EMT). Moreover, the epicardium is a source of secreted growth factors that promote myocardial growth. CCBE1 is a secreted extracellular matrix protein expressed by epicardial cells that is required for the formation of the primitive coronary plexus. However, the role of CCBE1 during epicardial development was still unknown. Here, using a Ccbe1 knockout (KO) mouse model, we observed that loss of CCBE1 leads to congenital heart defects including thinner and hyper-trabeculated ventricular myocardium. In addition, Ccbe1 mutant hearts displayed reduced proliferation of cardiomyocyte and epicardial cells. Epicardial outgrowth culture assay to assess epicardial-derived cells (EPDC) migration showed reduced invasion of the collagen gel by EPDCs in Ccbe1 KO epicardial explants. Ccbe1 KO hearts also displayed fewer nonmyocyte/nonendothelial cells intramyocardially with a reduced proliferation rate. Additionally, RNA-seq data and experimental validation by qRT-PCR showed a marked deregulation of EMT-related genes in developing Ccbe1 mutant hearts. Together, these findings indicate that the myocardium defects in Ccbe1 KO mice arise from disruption of epicardial development and function. MDPI 2022-10-20 /pmc/articles/PMC9604378/ /pubmed/36293499 http://dx.doi.org/10.3390/ijms232012642 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Bonet, Fernando Añez, Sabrina Brito Inácio, José Manuel Futschik, Matthias E. Belo, José Antonio CCBE1 Is Essential for Epicardial Function during Myocardium Development |
title | CCBE1 Is Essential for Epicardial Function during Myocardium Development |
title_full | CCBE1 Is Essential for Epicardial Function during Myocardium Development |
title_fullStr | CCBE1 Is Essential for Epicardial Function during Myocardium Development |
title_full_unstemmed | CCBE1 Is Essential for Epicardial Function during Myocardium Development |
title_short | CCBE1 Is Essential for Epicardial Function during Myocardium Development |
title_sort | ccbe1 is essential for epicardial function during myocardium development |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9604378/ https://www.ncbi.nlm.nih.gov/pubmed/36293499 http://dx.doi.org/10.3390/ijms232012642 |
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