Endothelial heterogeneity across distinct vascular beds during homeostasis and inflammation.
Ankit JambusariaZhigang HongLianghui ZhangShubhi SrivastavaArundhati JanaPeter T TothYang DaiAsrar B MalikJalees RehmanPublished in: eLife (2020)
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.
Keyphrases
- single cell
- endothelial cells
- rna seq
- genome wide
- nitric oxide
- high throughput
- high glucose
- genome wide identification
- oxidative stress
- vascular endothelial growth factor
- heart failure
- cell surface
- white matter
- gene expression
- skeletal muscle
- dna methylation
- bioinformatics analysis
- left ventricular
- single molecule
- multiple sclerosis
- transcription factor
- big data
- electronic health record
- artificial intelligence