Cargando…
Human Cardiac Organoids for Modeling Genetic Cardiomyopathy
Genetic cardiomyopathies are characterized by changes in the function and structure of the myocardium. The development of a novel in vitro model could help to better emulate healthy and diseased human heart conditions and may improve the understanding of disease mechanisms. In this study, for the fi...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7409052/ https://www.ncbi.nlm.nih.gov/pubmed/32698471 http://dx.doi.org/10.3390/cells9071733 |
_version_ | 1783567975000834048 |
---|---|
author | Filippo Buono, Michele von Boehmer, Lisa Strang, Jaan P. Hoerstrup, Simon Y. Emmert, Maximilian Nugraha, Bramasta |
author_facet | Filippo Buono, Michele von Boehmer, Lisa Strang, Jaan P. Hoerstrup, Simon Y. Emmert, Maximilian Nugraha, Bramasta |
author_sort | Filippo Buono, Michele |
collection | PubMed |
description | Genetic cardiomyopathies are characterized by changes in the function and structure of the myocardium. The development of a novel in vitro model could help to better emulate healthy and diseased human heart conditions and may improve the understanding of disease mechanisms. In this study, for the first time, we demonstrated the generation of cardiac organoids using a triculture approach of human induced pluripotent stem-cell-derived cardiomyocytes (hiPS-CMs)—from healthy subjects and cardiomyopathy patients—human cardiac microvascular endothelial cells (HCMECs) and human cardiac fibroblasts (HCFs). We assessed the organoids’ suitability as a 3D cellular model for the representation of phenotypical features of healthy and cardiomyopathic hearts. We observed clear differences in structure and beating behavior between the organoid groups, depending on the type of hiPS-CMs (healthy versus cardiomyopathic) used. Organoids may thus prove a promising tool for the design and testing of patient-specific treatments as well as provide a platform for safer and more efficacious drug development. |
format | Online Article Text |
id | pubmed-7409052 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-74090522020-08-26 Human Cardiac Organoids for Modeling Genetic Cardiomyopathy Filippo Buono, Michele von Boehmer, Lisa Strang, Jaan P. Hoerstrup, Simon Y. Emmert, Maximilian Nugraha, Bramasta Cells Article Genetic cardiomyopathies are characterized by changes in the function and structure of the myocardium. The development of a novel in vitro model could help to better emulate healthy and diseased human heart conditions and may improve the understanding of disease mechanisms. In this study, for the first time, we demonstrated the generation of cardiac organoids using a triculture approach of human induced pluripotent stem-cell-derived cardiomyocytes (hiPS-CMs)—from healthy subjects and cardiomyopathy patients—human cardiac microvascular endothelial cells (HCMECs) and human cardiac fibroblasts (HCFs). We assessed the organoids’ suitability as a 3D cellular model for the representation of phenotypical features of healthy and cardiomyopathic hearts. We observed clear differences in structure and beating behavior between the organoid groups, depending on the type of hiPS-CMs (healthy versus cardiomyopathic) used. Organoids may thus prove a promising tool for the design and testing of patient-specific treatments as well as provide a platform for safer and more efficacious drug development. MDPI 2020-07-20 /pmc/articles/PMC7409052/ /pubmed/32698471 http://dx.doi.org/10.3390/cells9071733 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Filippo Buono, Michele von Boehmer, Lisa Strang, Jaan P. Hoerstrup, Simon Y. Emmert, Maximilian Nugraha, Bramasta Human Cardiac Organoids for Modeling Genetic Cardiomyopathy |
title | Human Cardiac Organoids for Modeling Genetic Cardiomyopathy |
title_full | Human Cardiac Organoids for Modeling Genetic Cardiomyopathy |
title_fullStr | Human Cardiac Organoids for Modeling Genetic Cardiomyopathy |
title_full_unstemmed | Human Cardiac Organoids for Modeling Genetic Cardiomyopathy |
title_short | Human Cardiac Organoids for Modeling Genetic Cardiomyopathy |
title_sort | human cardiac organoids for modeling genetic cardiomyopathy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7409052/ https://www.ncbi.nlm.nih.gov/pubmed/32698471 http://dx.doi.org/10.3390/cells9071733 |
work_keys_str_mv | AT filippobuonomichele humancardiacorganoidsformodelinggeneticcardiomyopathy AT vonboehmerlisa humancardiacorganoidsformodelinggeneticcardiomyopathy AT strangjaan humancardiacorganoidsformodelinggeneticcardiomyopathy AT phoerstrupsimon humancardiacorganoidsformodelinggeneticcardiomyopathy AT yemmertmaximilian humancardiacorganoidsformodelinggeneticcardiomyopathy AT nugrahabramasta humancardiacorganoidsformodelinggeneticcardiomyopathy |