Endothelial heterogeneity across distinct vascular beds during homeostasis and inflammation

被引:211
作者
Jambusaria, Ankit [1 ,2 ,3 ]
Hong, Zhigang [1 ]
Zhang, Lianghui [1 ]
Srivastava, Shubhi [1 ]
Jana, Arundhati [4 ]
Toth, Peter T. [1 ,5 ]
Dai, Yang [2 ,3 ]
Malik, Asrar B. [1 ]
Rehman, Jalees [1 ,4 ]
机构
[1] Univ Illinois, Coll Med, Dept Pharmacol, Chicago, IL 60612 USA
[2] Univ Illinois, Dept Bioengn, Coll Engn, Chicago, IL USA
[3] Coll Med, Chicago, IL USA
[4] Univ Illinois, Coll Med, Dept Med, Div Cardiol, Chicago, IL 60607 USA
[5] Univ Illinois, Res Resources Ctr, Chicago, IL USA
基金
美国国家卫生研究院;
关键词
GENOME-WIDE EXPRESSION; RNA SEQUENCING DATA; SINGLE-CELL; MOLECULAR SIGNATURES; MESSENGER-RNA; GENE; SEQ; PACKAGE; MYOSIN; ALPHA;
D O I
10.7554/eLife.51413
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
引用
收藏
页数:32
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