Coronary blood vessels from distinct origins converge to equivalent states during mouse and human development

• Published in: eLife Vol. 10
• Main Authors: Phansalkar, Ragini, Krieger, Josephine, Zhao, Mingming, Kolluru, Sai Saroja, Jones, Robert C, Quake, Stephen R, Weissman, Irving, Bernstein, Daniel, Winn, Virginia D, D'Amato, Gaetano, Red-Horse, Kristy
• Format: Journal Article
• Language: English
• Published: England eLife Sciences Publications Ltd 15.12.2021; eLife Sciences Publications, Ltd
• Subjects: Angiogenesis; Animals; Approximation; Blood flow; Blood vessels; Cell cycle; Cell differentiation; Cell fate; convergent differentiation; Coronary vessels; Coronary Vessels - embryology; Datasets; Developmental Biology; Developmental plasticity; Embryo, Mammalian - metabolism; Embryogenesis; Embryonic Development; Endothelial cells; Endothelial Cells - metabolism; Gene expression; Heart; heart development; human mouse comparison; Humans; Hypoxia; Localization; Mice; Progenitor cells; RNA-Seq; Septum; Single-Cell Analysis; Sinuses; Transcription; vascular development; mouse; heart development; vascular development; developmental biology; human mouse comparison; human; convergent differentiation
• ISSN: 2050-084X; 2050-084X
• DOI: 10.7554/eLife.70246

Most cell fate trajectories during development follow a diverging, tree-like branching pattern, but the opposite can occur when distinct progenitors contribute to the same cell type. During this convergent differentiation, it is unknown if cells 'remember' their origins transcriptionally or whether this influences cell behavior. Most coronary blood vessels of the heart develop from two different progenitor sources-the endocardium (Endo) and sinus venosus (SV)-but whether transcriptional or functional differences related to origin are retained is unknown. We addressed this by combining lineage tracing with single-cell RNA sequencing (scRNAseq) in embryonic and adult mouse hearts. Shortly after coronary development begins, capillary endothelial cells (ECs) transcriptionally segregated into two states that retained progenitor-specific gene expression. Later in development, when the coronary vasculature is well established but still remodeling, capillary ECs again segregated into two populations, but transcriptional differences were primarily related to tissue localization rather than lineage. Specifically, ECs in the heart septum expressed genes indicative of increased local hypoxia and decreased blood flow. Adult capillary ECs were more homogeneous with respect to both lineage and location. In agreement, SV- and Endo-derived ECs in adult hearts displayed similar responses to injury. Finally, scRNAseq of developing human coronary vessels indicated that the human heart followed similar principles. Thus, over the course of development, transcriptional heterogeneity in coronary ECs is first influenced by lineage, then by location, until heterogeneity declines in the homeostatic adult heart. These results highlight the plasticity of ECs during development, and the validity of the mouse as a model for human coronary development.