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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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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. |
format | Online Article Text |
id | pubmed-10227949 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
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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