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

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          Abstract

          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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          Most cited references72

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          Multipotent embryonic isl1+ progenitor cells lead to cardiac, smooth muscle, and endothelial cell diversification.

          Cardiogenesis requires the generation of endothelial, cardiac, and smooth muscle cells, thought to arise from distinct embryonic precursors. We use genetic fate-mapping studies to document that isl1(+) precursors from the second heart field can generate each of these diverse cardiovascular cell types in vivo. Utilizing embryonic stem (ES) cells, we clonally amplified a cellular hierarchy of isl1(+) cardiovascular progenitors, which resemble the developmental precursors in the embryonic heart. The transcriptional signature of isl1(+)/Nkx2.5(+)/flk1(+) defines a multipotent cardiovascular progenitor, which can give rise to cells of all three lineages. These studies document a developmental paradigm for cardiogenesis, where muscle and endothelial lineage diversification arises from a single cell-level decision of a multipotent isl1(+) cardiovascular progenitor cell (MICP). The discovery of ES cell-derived MICPs suggests a strategy for cardiovascular tissue regeneration via their isolation, renewal, and directed differentiation into specific mature cardiac, pacemaker, smooth muscle, and endothelial cell types.
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            Cardiomyocyte Regeneration

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              Cardioids reveal self-organizing principles of human cardiogenesis

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                Author and article information

                Contributors
                Journal
                Front Cell Dev Biol
                Front Cell Dev Biol
                Front. Cell Dev. Biol.
                Frontiers in Cell and Developmental Biology
                Frontiers Media S.A.
                2296-634X
                15 May 2023
                2023
                : 11
                : 1111684
                Affiliations
                [1] 1 First Department of Medicine, Cardiology , Klinikum Rechts der Isar , School of Medicine and Health , Technical University of Munich , Munich, Germany
                [2] 2 German Center for Cardiovascular Research (DZHK) , Munich Heart Alliance , Munich, Germany
                [3] 3 Regenerative Medicine in Cardiovascular Diseases , First Department of Medicine , Klinikum Rechts der Isar , School of Medicine and Health , Technical University of Munich , Munich, Germany
                [4] 4 Department of Surgery , Yale University School of Medicine , New Haven, CT, United States
                Author notes

                Edited by: Yongye Huang, Northeastern University, China

                Reviewed by: Alexandre R. Colas, Sanford Burnham Prebys Medical Discovery Institute, United States

                Chikai Zhou, Chinese Academy of Agricultural Sciences, China

                Loukia Yiangou, Leiden University Medical Center (LUMC), Netherlands

                *Correspondence: Alessandra Moretti, amoretti@ 123456mytum.de ; Monika Nowak-Imialek, monika.nowak-imialek@ 123456tum.de
                [ † ]

                These authors have contributed equally to this work

                Article
                1111684
                10.3389/fcell.2023.1111684
                10227949
                37261075
                989cb3bd-9a7a-446d-a292-85967a7d8666
                Copyright © 2023 Rawat, Kornherr, Zawada, Bakhshiyeva, Kupatt, Laugwitz, Bähr, Dorn, Moretti and Nowak-Imialek.

                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.

                History
                : 29 November 2022
                : 21 April 2023
                Funding
                This work was supported by the European Research Council (ERC) (grant 788381 to AM and grant 101021043 to CK). Several authors of this study are principal investigators of the Transregio Research Units 152 and 267 funded by the German Research Foundation.
                Categories
                Cell and Developmental Biology
                Original Research
                Custom metadata
                Stem Cell Research

                pig,heart development,porcine expanded pluripotent stem cells,cardiac progenitor cells,epicardial cells,cardiomyocyte,cardiac differentiation

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