Skip to main content
. 2020 Mar 30:cvaa078. doi: 10.1093/cvr/cvaa078

Figure 1.

Figure 1

(A) The spatial and protein docking of human ACE2 protein and Spike protein of SARS-CoV-2. (B) ACE2 mRNA expression level across human organs by GTEx; (C) t-SNE plot of cell clusters in human hearts; (D). Heatmap of gene signatures of each cell type with marker genes labels; (E) Feature plot of ACE2 expression across cell types in the heart; (F) Violin plot reveals high expression of ACE2 in pericyte, and this cell type highly expresses ABCC9 (pericyte marker), but not MYH11 (SMC marker gene); (G) Violin plot reveals specifically high expression of CD209 in macrophage (co-expression with CD163); (H) Cell–cell interaction between pericyte (ligand) and other cell types (receptor) (left panel), and dominant cross-talks from pericyte to endothelial cell (EC) (right panel); (I) Cell–cell interaction between macrophage (ligand) and other cell types (receptor) (left panel), and dominant cross-talks from macrophage to EC (right panel); (J) ACE2 mRNA is increased in failing hearts (n = 40) compared to normal donors (n = 15) by RNA sequencing (P < 0.0001 by Student’s t-test); (K) ACE2 protein is increased in failing hearts (n = 8) compared to normal donors (n = 8) by proteomics (P < 0.0001 by Student’s t-test).