Publication: Myocardium and endocardium of the early mammalian heart tube arise from independent multipotent lineages specified at the primitive streak.
| dc.contributor.author | Sendra, Miquel | |
| dc.contributor.author | McDole, Katie | |
| dc.contributor.author | de Dios Hourcade, Juan | |
| dc.contributor.author | Temiño, Susana | |
| dc.contributor.author | Raiola, Morena | |
| dc.contributor.author | Guignard, Léo | |
| dc.contributor.author | Keller, Philipp J | |
| dc.contributor.author | Domínguez, Jorge N | |
| dc.contributor.author | Torres, Miguel | |
| dc.contributor.funder | Fundación La Caixa | |
| dc.contributor.funder | Comunidad de Madrid (España) | |
| dc.date.accessioned | 2026-03-16T12:11:07Z | |
| dc.date.available | 2026-03-16T12:11:07Z | |
| dc.date.issued | 2025-09-22 | |
| dc.description.abstract | The formation of the primitive heart tube from cardiomyocytes and endocardial cells is a key event in mammalian development. Previous studies suggested that cardiomyocytes and endocardial cells segregate from a shared cardiac progenitor around the onset of gastrulation, yet their lineage relationship with other mesodermal tissues remains unclear. Using retrospective and prospective clonal analyses in mouse embryos, we traced cardiomyocyte and endocardial progenitors from the primitive streak to the heart tube. Our results identify two independent mesodermal populations specified around gastrulation onset. While each of these populations is unipotent in producing cardiomyocytes or endocardium, they retain multipotency and contribute to different subsets of non-cardiac mesoderm. Nonetheless, live imaging identifies simultaneous ingression and intermingling of these two mesodermal lineages in the primitive streak, showing their coordinated specification and migration. The proposed model for cardiac progenitor specification will help understanding the origins of congenital heart diseases and designing tissue engineering strategies. | |
| dc.description.peerreviewed | Sí | |
| dc.description.tableofcontents | We thank members of the Torres group for inspiring discussions and advice. We thank members of the Microscopy and Dynamic Imaging, Transgenesis, and Animal Facility CNIC units for excellent support. We thank ‘‘La Caixa’’ Foundation (ID 100010434) for the fellowship that supported M.S. stipend (LCF/BQ/DE18/11670014). We also thank the Company of Biologists for the traveling fellowship that made possible M.S. stay at Janelia Research Institute with K.M., L.G., and P.J.K. (DEVTF181145). This work was funded by grants PGC2018-096486-B-I00 and PID2022-140058NB-C31 from the Agencia Estatal de Investigación to M.T.; European Commission H2020 Program grant SC1-BHC-07-2019. Ref. 874764 ‘‘REANIMA’’ to M.T., Comunidad de Madrid grant P2022/BMD-7245 CARDIOBOOST-CM to M.T. The CNIC Unit of Microscopy and Dynamic Imaging is supported by FEDER ‘‘Una manera de hacer Europa’’ (ReDIB ICTS infrastructure TRIMA@CNIC, MCIN). The CNIC is supported by the Ministerio de Ciencia e Innovación and the Pro CNIC Foundation and is a Severo Ochoa Center of Excellence (Grant number CEX2020-001041-S, funded by MICIU/AEI 10.13039/501100011033). | |
| dc.identifier.citation | Dev Cell. 2025 Sep 22;60(18):2434-2444.e5. | |
| dc.identifier.journal | Developmental Cell | |
| dc.identifier.pubmedID | 40436021 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.12105/27316 | |
| dc.language.iso | eng | |
| dc.publisher | Cell Press | |
| dc.relation.isreferencedby | PubMed | |
| dc.relation.projectID | info:eu-repo/grantAgreement/EC/H2020/SC1-BHC-07-2019 | |
| dc.relation.projectID | info:eu-repo/grantAgreement/EC/H2020/874764 | |
| dc.relation.projectID | info:eu-repo/grantAgreement/ES/LCF/BQ/DE18/11670014 | |
| dc.relation.projectID | info:eu-repo/grantAgreement/ES/PGC2018-096486-B-I00 | |
| dc.relation.projectID | info:eu-repo/grantAgreement/ES/PID2022-140058NB-C31 | |
| dc.relation.projectID | info:eu-repo/grantAgreement/ES/MICIU/AEI 10.13039/501100011033/CEX2020-001041-S | |
| dc.relation.publisherversion | https://doi.org/10.1016/j.devcel.2025.05.002 | |
| dc.repisalud.institucion | CNIC | |
| dc.repisalud.orgCNIC | CNIC::Grupos de investigación::Control Genético del Desarrollo y Regeneración de Órganos | |
| dc.rights.accessRights | open access | |
| dc.rights.license | Attribution-NonCommercial-NoDerivatives 4.0 International | en |
| dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ | |
| dc.subject | cardiac progenitors | |
| dc.subject | cardiomyocytes | |
| dc.subject | cell fate | |
| dc.subject | clonal analysis | |
| dc.subject | endocardial cells | |
| dc.subject | heart development | |
| dc.subject | lineage specification | |
| dc.subject | lineage tracing | |
| dc.subject | live imaging | |
| dc.subject | mesoderm | |
| dc.title | Myocardium and endocardium of the early mammalian heart tube arise from independent multipotent lineages specified at the primitive streak. | |
| dc.type | research article | |
| dc.type.hasVersion | VoR | |
| dspace.entity.type | Publication |
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