Department of Pharmacology, The University of Illinois College of Medicine, Chicago, United States; Department of Bioengineering, The University of Illinois College of Engineering and College of Medicine, Chicago, United States
Zhigang Hong
Department of Pharmacology, The University of Illinois College of Medicine, Chicago, United States
Lianghui Zhang
Department of Pharmacology, The University of Illinois College of Medicine, Chicago, United States
Shubhi Srivastava
Department of Pharmacology, The University of Illinois College of Medicine, Chicago, United States
Arundhati Jana
Division of Cardiology, Department of Medicine, The University of Illinois College of Medicine, Chicago, United States
Peter T Toth
Department of Pharmacology, The University of Illinois College of Medicine, Chicago, United States; Research Resources Center, University of Illinois, Chicago, United States
Yang Dai
Department of Bioengineering, The University of Illinois College of Engineering and College of Medicine, Chicago, United States
Department of Pharmacology, The University of Illinois College of Medicine, Chicago, United States; Division of Cardiology, Department of Medicine, The University of Illinois College of Medicine, Chicago, United States
Blood vessels are lined by endothelial cells engaged in distinct organ-specific functions but little is known about their characteristic gene expression profiles. RNA-Sequencing of the brain, lung, and heart endothelial translatome identified specific pathways, transporters and cell-surface markers expressed in the endothelium of each organ, which can be visualized at http://www.rehmanlab.org/ribo. We found that endothelial cells express genes typically found in the surrounding tissues such as synaptic vesicle genes in the brain endothelium and cardiac contractile genes in the heart endothelium. Complementary analysis of endothelial single cell RNA-Seq data identified the molecular signatures shared across the endothelial translatome and single cell transcriptomes. The tissue-specific heterogeneity of the endothelium is maintained during systemic in vivo inflammatory injury as evidenced by the distinct responses to inflammatory stimulation. Our study defines endothelial heterogeneity and plasticity and provides a molecular framework to understand organ-specific vascular disease mechanisms and therapeutic targeting of individual vascular beds.