| Literature DB >> 29371425 |
Fabienne Lescroart1, Xiaonan Wang2,3, Xionghui Lin1, Benjamin Swedlund1, Souhir Gargouri1, Adriana Sànchez-Dànes1, Victoria Moignard2,3, Christine Dubois1, Catherine Paulissen1, Sarah Kinston2,3, Berthold Göttgens4,3, Cédric Blanpain5,6.
Abstract
Mouse heart development arises from Mesp1-expressing cardiovascular progenitors (CPs) that are specified during gastrulation. The molecular processes that control early regional and lineage segregation of CPs have been unclear. We performed single-cell RNA sequencing of wild-type and Mesp1-null CPs in mice. We showed that populations of Mesp1 CPs are molecularly distinct and span the continuum between epiblast and later mesodermal cells, including hematopoietic progenitors. Single-cell transcriptome analysis of Mesp1-deficient CPs showed that Mesp1 is required for the exit from the pluripotent state and the induction of the cardiovascular gene expression program. We identified distinct populations of Mesp1 CPs that correspond to progenitors committed to different cell lineages and regions of the heart, identifying the molecular features associated with early lineage restriction and regional segregation of the heart at the early stage of mouse gastrulation.Entities:
Mesh:
Substances:
Year: 2018 PMID: 29371425 PMCID: PMC6556615 DOI: 10.1126/science.aao4174
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728