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CDH18 is a fetal epicardial biomarker regulating differentiation towards vascular smooth muscle cells
The epicardium is a mesothelial layer covering the myocardium serving as a progenitor source during cardiac development. The epicardium reactivates upon cardiac injury supporting cardiac repair and regeneration. Fine-tuned balanced signaling regulates cell plasticity and cell-fate decisions of epica...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8810917/ https://www.ncbi.nlm.nih.gov/pubmed/35110584 http://dx.doi.org/10.1038/s41536-022-00207-w |
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author | Junghof, Julia Kogure, Yuta Yu, Tian Verdugo-Sivianes, Eva María Narita, Megumi Lucena-Cacace, Antonio Yoshida, Yoshinori |
author_facet | Junghof, Julia Kogure, Yuta Yu, Tian Verdugo-Sivianes, Eva María Narita, Megumi Lucena-Cacace, Antonio Yoshida, Yoshinori |
author_sort | Junghof, Julia |
collection | PubMed |
description | The epicardium is a mesothelial layer covering the myocardium serving as a progenitor source during cardiac development. The epicardium reactivates upon cardiac injury supporting cardiac repair and regeneration. Fine-tuned balanced signaling regulates cell plasticity and cell-fate decisions of epicardial-derived cells (EPCDs) via epicardial-to-mesenchymal transition (EMT). However, powerful tools to investigate epicardial function, including markers with pivotal roles in developmental signaling, are still lacking. Here, we recapitulated epicardiogenesis using human induced pluripotent stem cells (hiPSCs) and identified type II classical cadherin CDH18 as a biomarker defining lineage specification in human active epicardium. The loss of CDH18 led to the onset of EMT and specific differentiation towards cardiac smooth muscle cells. Furthermore, GATA4 regulated epicardial CDH18 expression. These results highlight the importance of tracing CDH18 expression in hiPSC-derived epicardial cells, providing a model for investigating epicardial function in human development and disease and enabling new possibilities for regenerative medicine. |
format | Online Article Text |
id | pubmed-8810917 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-88109172022-02-10 CDH18 is a fetal epicardial biomarker regulating differentiation towards vascular smooth muscle cells Junghof, Julia Kogure, Yuta Yu, Tian Verdugo-Sivianes, Eva María Narita, Megumi Lucena-Cacace, Antonio Yoshida, Yoshinori NPJ Regen Med Article The epicardium is a mesothelial layer covering the myocardium serving as a progenitor source during cardiac development. The epicardium reactivates upon cardiac injury supporting cardiac repair and regeneration. Fine-tuned balanced signaling regulates cell plasticity and cell-fate decisions of epicardial-derived cells (EPCDs) via epicardial-to-mesenchymal transition (EMT). However, powerful tools to investigate epicardial function, including markers with pivotal roles in developmental signaling, are still lacking. Here, we recapitulated epicardiogenesis using human induced pluripotent stem cells (hiPSCs) and identified type II classical cadherin CDH18 as a biomarker defining lineage specification in human active epicardium. The loss of CDH18 led to the onset of EMT and specific differentiation towards cardiac smooth muscle cells. Furthermore, GATA4 regulated epicardial CDH18 expression. These results highlight the importance of tracing CDH18 expression in hiPSC-derived epicardial cells, providing a model for investigating epicardial function in human development and disease and enabling new possibilities for regenerative medicine. Nature Publishing Group UK 2022-02-02 /pmc/articles/PMC8810917/ /pubmed/35110584 http://dx.doi.org/10.1038/s41536-022-00207-w 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 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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Junghof, Julia Kogure, Yuta Yu, Tian Verdugo-Sivianes, Eva María Narita, Megumi Lucena-Cacace, Antonio Yoshida, Yoshinori CDH18 is a fetal epicardial biomarker regulating differentiation towards vascular smooth muscle cells |
title | CDH18 is a fetal epicardial biomarker regulating differentiation towards vascular smooth muscle cells |
title_full | CDH18 is a fetal epicardial biomarker regulating differentiation towards vascular smooth muscle cells |
title_fullStr | CDH18 is a fetal epicardial biomarker regulating differentiation towards vascular smooth muscle cells |
title_full_unstemmed | CDH18 is a fetal epicardial biomarker regulating differentiation towards vascular smooth muscle cells |
title_short | CDH18 is a fetal epicardial biomarker regulating differentiation towards vascular smooth muscle cells |
title_sort | cdh18 is a fetal epicardial biomarker regulating differentiation towards vascular smooth muscle cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8810917/ https://www.ncbi.nlm.nih.gov/pubmed/35110584 http://dx.doi.org/10.1038/s41536-022-00207-w |
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