The deployment of cell lineages that form the mammalian heart
- PMID: 30266935
- DOI: 10.1038/s41569-018-0086-9
The deployment of cell lineages that form the mammalian heart
Abstract
The function of the mammalian heart depends on the interplay between different cardiac cell types. The deployment of these cells, with precise spatiotemporal regulation, is also important during development to establish the heart structure. In this Review, we discuss the diverse origins of cardiac cell types and the lineage relationships between cells of a given type that contribute to different parts of the heart. The emerging lineage tree shows the progression of cell fate diversification, with patterning cues preceding cell type segregation, as well as points of convergence, with overlapping lineages contributing to a given tissue. Several cell lineage markers have been identified. However, caution is required with genetic-tracing experiments in comparison with clonal analyses. Genetic studies on cell populations provided insights into the mechanisms for lineage decisions. In the past 3 years, results of single-cell transcriptomics are beginning to reveal cell heterogeneity and early developmental trajectories. Equating this information with the in vivo location of cells and their lineage history is a current challenge. Characterization of the progenitor cells that form the heart and of the gene regulatory networks that control their deployment is of major importance for understanding the origin of congenital heart malformations and for producing cardiac tissue for use in regenerative medicine.
Similar articles
-
Notch and interacting signalling pathways in cardiac development, disease, and regeneration.Nat Rev Cardiol. 2018 Nov;15(11):685-704. doi: 10.1038/s41569-018-0100-2. Nat Rev Cardiol. 2018. PMID: 30287945 Review.
-
Critical role of phosphodiesterase 2A in mouse congenital heart defects.Cardiovasc Res. 2018 May 1;114(6):830-845. doi: 10.1093/cvr/cvy030. Cardiovasc Res. 2018. PMID: 29409032
-
Epicardium-derived fibroblasts in heart development and disease.J Mol Cell Cardiol. 2016 Feb;91:23-7. doi: 10.1016/j.yjmcc.2015.12.019. Epub 2015 Dec 22. J Mol Cell Cardiol. 2016. PMID: 26718723 Free PMC article. Review.
-
Building the mammalian heart from two sources of myocardial cells.Nat Rev Genet. 2005 Nov;6(11):826-35. doi: 10.1038/nrg1710. Nat Rev Genet. 2005. PMID: 16304598 Review.
-
Direct cardiac reprogramming: progress and challenges in basic biology and clinical applications.Circ Res. 2015 Apr 10;116(8):1378-91. doi: 10.1161/CIRCRESAHA.116.305374. Circ Res. 2015. PMID: 25858064 Review.
Cited by
-
Concordant and Heterogeneity of Single-Cell Transcriptome in Cardiac Development of Human and Mouse.Front Genet. 2022 Jun 27;13:892766. doi: 10.3389/fgene.2022.892766. eCollection 2022. Front Genet. 2022. PMID: 35832197 Free PMC article.
-
Multiplexed Single Cell mRNA Sequencing Analysis of Mouse Embryonic Cells.J Vis Exp. 2020 Jan 7;(155):10.3791/60647. doi: 10.3791/60647. J Vis Exp. 2020. PMID: 31984954 Free PMC article.
-
A patterned human primitive heart organoid model generated by pluripotent stem cell self-organization.Nat Commun. 2023 Dec 12;14(1):8245. doi: 10.1038/s41467-023-43999-1. Nat Commun. 2023. PMID: 38086920 Free PMC article.
-
Ventricular, atrial, and outflow tract heart progenitors arise from spatially and molecularly distinct regions of the primitive streak.PLoS Biol. 2021 May 17;19(5):e3001200. doi: 10.1371/journal.pbio.3001200. eCollection 2021 May. PLoS Biol. 2021. PMID: 33999917 Free PMC article.
-
The pericardium forms as a distinct structure during heart formation.bioRxiv [Preprint]. 2024 Sep 28:2024.09.18.613484. doi: 10.1101/2024.09.18.613484. bioRxiv. 2024. PMID: 39345600 Free PMC article. Preprint.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Miscellaneous