TY - JOUR
T1 - Recapitulating porcine cardiac development in vitro
T2 - from expanded potential stem cell to embryo culture models
AU - Rawat, Hilansi
AU - Kornherr, Jessica
AU - Zawada, Dorota
AU - Bakhshiyeva, Sara
AU - Kupatt, Christian
AU - Laugwitz, Karl Ludwig
AU - Bähr, Andrea
AU - Dorn, Tatjana
AU - Moretti, Alessandra
AU - Nowak-Imialek, Monika
N1 - Publisher Copyright:
Copyright © 2023 Rawat, Kornherr, Zawada, Bakhshiyeva, Kupatt, Laugwitz, Bähr, Dorn, Moretti and Nowak-Imialek.
PY - 2023
Y1 - 2023
N2 - 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.
AB - 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.
KW - cardiac differentiation
KW - cardiac progenitor cells
KW - cardiomyocyte
KW - epicardial cells
KW - heart development
KW - pig
KW - porcine expanded pluripotent stem cells
UR - http://www.scopus.com/inward/record.url?scp=85161040448&partnerID=8YFLogxK
U2 - 10.3389/fcell.2023.1111684
DO - 10.3389/fcell.2023.1111684
M3 - Article
AN - SCOPUS:85161040448
SN - 2296-634X
VL - 11
JO - Frontiers in Cell and Developmental Biology
JF - Frontiers in Cell and Developmental Biology
M1 - 1111684
ER -