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Apical Resection Mouse Model to Study Early Mammalian Heart Regeneration
Published on: January 23, 2016
The deployment of cell lineages that form the mammalian heart
Sigolène M Meilhac1,2, Margaret E Buckingham3
1Imagine Institut Pasteur, Laboratory of Heart Morphogenesis, Paris, France. sigolene.meilhac@pasteur.fr.
Insights
Understanding cardiac cell origins and lineage is key to heart development and disease. This review explores cardiac cell diversity, developmental trajectories, and their implications for congenital heart malformations and regenerative medicine.
Area of Science:
- Cardiovascular Biology
- Developmental Biology
- Cell Biology
Background:
- The mammalian heart's function relies on the coordinated interplay of diverse cardiac cell types.
- Precise spatiotemporal regulation of cell deployment is crucial for establishing heart structure during development.
Purpose of the Study:
- To review the diverse origins of cardiac cell types and their lineage relationships.
- To elucidate the progression of cell fate diversification and identify points of lineage convergence during heart development.
Main Methods:
- Analysis of emerging lineage trees and genetic studies on cell populations.
- Integration of single-cell transcriptomics data with in vivo cell location and lineage history.
Main Results:
- Identified diverse origins and lineage relationships among cardiac cell types contributing to different heart regions.
- Revealed cell fate diversification progression, with patterning cues preceding cell type segregation.
- Highlighted cell heterogeneity and early developmental trajectories through single-cell transcriptomics.
Conclusions:
- Characterizing cardiac progenitor cells and their gene regulatory networks is vital for understanding congenital heart malformations.
- This knowledge is essential for advancing cardiac tissue production in regenerative medicine.
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.
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