A single-cell time-series atlas of endothelial cell embryonic development
Summary
Endothelial cells (ECs) are essential components of the vertebrate circulatory system; however, a comprehensive atlas characterizing how ECs acquire organ-specific transcriptomic heterogeneity has not been established. Here, we generated a time-series endothelial resource covering the entirety of mouse embryonic development, including 26 time points and 8 organs. Time-series multi-organ comparison revealed emergence timing and lineage trajectory of organotypic ECs together with organ-speci
Content
# A single-cell time-series atlas of endothelial cell embryonic development
*Published: 2026 Mar 5*
Endothelial cells (ECs) are essential components of the vertebrate circulatory
system; however, a comprehensive atlas characterizing how ECs acquire
organ-specific transcriptomic heterogeneity has not been established. Here, we
generated a time-series endothelial resource covering the entirety of mouse
embryonic development, including 26 time points and 8 organs. Time-series
multi-organ comparison revealed emergence timing and lineage trajectory of
organotypic ECs together with organ-specific genes and pathways. Using these
resources, we found that most ECs showed distinguishable organ specificity
before late gestation. The organotypic EC-enriched genes were associated with
vascular function in the organs. Human and mouse pulmonary ECs underwent an
evolutionarily conserved transcriptional transition. Endothelial-specific
knockout of Casz1, a pulmonary EC-enriched transcription factor, resulted in
impaired vascular growth, disturbed pulmonary endothelial organotypic
differentiation, and deficient epithelial-EC crosstalk. Our work provides a
powerful endothelial resource that reveals fundamental principles of
organ-specific EC differentiation and uncovers previously unknown molecular
mechanisms governing lung-specific vascular development.
DOI: 10.1016/j.cell.2026.01.002