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Recapitulating porcine cardiac development in vitro: from expanded potential stem cell to embryo culture models

Domestic pigs (Sus scrofa) share many genetic, anatomical, and physiological traits with humans and therefore constitute an excellent preclinical animal model. Fundamental understanding of the cellular and molecular processes governing early porcine cardiogenesis is critical for developing advanced...

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Autores principales: Rawat, Hilansi, Kornherr, Jessica, Zawada, Dorota, Bakhshiyeva, Sara, Kupatt, Christian, Laugwitz, Karl-Ludwig, Bähr, Andrea, Dorn, Tatjana, Moretti, Alessandra, Nowak-Imialek, Monika
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10227949/
https://www.ncbi.nlm.nih.gov/pubmed/37261075
http://dx.doi.org/10.3389/fcell.2023.1111684
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author Rawat, Hilansi
Kornherr, Jessica
Zawada, Dorota
Bakhshiyeva, Sara
Kupatt, Christian
Laugwitz, Karl-Ludwig
Bähr, Andrea
Dorn, Tatjana
Moretti, Alessandra
Nowak-Imialek, Monika
author_facet Rawat, Hilansi
Kornherr, Jessica
Zawada, Dorota
Bakhshiyeva, Sara
Kupatt, Christian
Laugwitz, Karl-Ludwig
Bähr, Andrea
Dorn, Tatjana
Moretti, Alessandra
Nowak-Imialek, Monika
author_sort Rawat, Hilansi
collection PubMed
description Domestic pigs (Sus scrofa) share many genetic, anatomical, and physiological traits with humans and therefore constitute an excellent preclinical animal model. Fundamental understanding of the cellular and molecular processes governing early porcine cardiogenesis is critical for developing advanced porcine models used for the study of heart diseases and new regenerative therapies. Here, we provide a detailed characterization of porcine cardiogenesis based on fetal porcine hearts at various developmental stages and cardiac cells derived from porcine expanded pluripotent stem cells (pEPSCs), i.e., stem cells having the potential to give rise to both embryonic and extraembryonic tissue. We notably demonstrate for the first time that pEPSCs can differentiate into cardiovascular progenitor cells (CPCs), functional cardiomyocytes (CMs), epicardial cells and epicardial-derived cells (EPDCs) in vitro. Furthermore, we present an enhanced system for whole-embryo culture which allows continuous ex utero development of porcine post-implantation embryos from the cardiac crescent stage (ED14) up to the cardiac looping (ED17) stage. These new techniques provide a versatile platform for studying porcine cardiac development and disease modeling.
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spelling pubmed-102279492023-05-31 Recapitulating porcine cardiac development in vitro: from expanded potential stem cell to embryo culture models Rawat, Hilansi Kornherr, Jessica Zawada, Dorota Bakhshiyeva, Sara Kupatt, Christian Laugwitz, Karl-Ludwig Bähr, Andrea Dorn, Tatjana Moretti, Alessandra Nowak-Imialek, Monika Front Cell Dev Biol Cell and Developmental Biology Domestic pigs (Sus scrofa) share many genetic, anatomical, and physiological traits with humans and therefore constitute an excellent preclinical animal model. Fundamental understanding of the cellular and molecular processes governing early porcine cardiogenesis is critical for developing advanced porcine models used for the study of heart diseases and new regenerative therapies. Here, we provide a detailed characterization of porcine cardiogenesis based on fetal porcine hearts at various developmental stages and cardiac cells derived from porcine expanded pluripotent stem cells (pEPSCs), i.e., stem cells having the potential to give rise to both embryonic and extraembryonic tissue. We notably demonstrate for the first time that pEPSCs can differentiate into cardiovascular progenitor cells (CPCs), functional cardiomyocytes (CMs), epicardial cells and epicardial-derived cells (EPDCs) in vitro. Furthermore, we present an enhanced system for whole-embryo culture which allows continuous ex utero development of porcine post-implantation embryos from the cardiac crescent stage (ED14) up to the cardiac looping (ED17) stage. These new techniques provide a versatile platform for studying porcine cardiac development and disease modeling. Frontiers Media S.A. 2023-05-15 /pmc/articles/PMC10227949/ /pubmed/37261075 http://dx.doi.org/10.3389/fcell.2023.1111684 Text en Copyright © 2023 Rawat, Kornherr, Zawada, Bakhshiyeva, Kupatt, Laugwitz, Bähr, Dorn, Moretti and Nowak-Imialek. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cell and Developmental Biology
Rawat, Hilansi
Kornherr, Jessica
Zawada, Dorota
Bakhshiyeva, Sara
Kupatt, Christian
Laugwitz, Karl-Ludwig
Bähr, Andrea
Dorn, Tatjana
Moretti, Alessandra
Nowak-Imialek, Monika
Recapitulating porcine cardiac development in vitro: from expanded potential stem cell to embryo culture models
title Recapitulating porcine cardiac development in vitro: from expanded potential stem cell to embryo culture models
title_full Recapitulating porcine cardiac development in vitro: from expanded potential stem cell to embryo culture models
title_fullStr Recapitulating porcine cardiac development in vitro: from expanded potential stem cell to embryo culture models
title_full_unstemmed Recapitulating porcine cardiac development in vitro: from expanded potential stem cell to embryo culture models
title_short Recapitulating porcine cardiac development in vitro: from expanded potential stem cell to embryo culture models
title_sort recapitulating porcine cardiac development in vitro: from expanded potential stem cell to embryo culture models
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10227949/
https://www.ncbi.nlm.nih.gov/pubmed/37261075
http://dx.doi.org/10.3389/fcell.2023.1111684
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