Cardiorenal Tissues Express SARS-CoV-2 Entry Genes and Basigin (BSG/CD147) Increases With Age in Endothelial Cells
Author(s) -
Blerina AhmetajShala,
Ricky Vaja,
Santosh S. Atanur,
Peter M. George,
Nicholas S. Kirkby,
Jane A. Mitchell
Publication year - 2020
Publication title -
jacc basic to translational science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.549
H-Index - 31
ISSN - 2452-302X
DOI - 10.1016/j.jacbts.2020.09.010
Subject(s) - basigin , thrombotic microangiopathy , coronavirus , immunology , biology , transcriptome , endothelium , inflammation , medicine , virology , gene , disease , covid-19 , gene expression , matrix metalloproteinase , genetics , infectious disease (medical specialty)
Vascular and cardiovascular inflammation and thrombosis occur in patients with severe coronavirus disease-2019 (COVID-19). Advancing age is the most significant risk factor for severe COVID-19. Using transcriptomic databases, the authors found that: 1) cardiovascular tissues and endothelial cells express putative genes for severe acute respiratory syndrome coronavirus-2 infection, including angiotensin-converting enzyme 2 ( ACE2 ) and basigin ( BSG ); 2) severe acute respiratory syndrome coronavirus-2 receptor pathways ACE2 /transmembrane serine protease 2 and BSG /peptidylprolyl isomerase B(A) polarize to lung/epithelium and vessel/endothelium, respectively; 3) expression of host genes is relatively stable with age; and 4) notable exceptions are ACE2 , which decreases with age in some tissues, and BSG , which increases with age in endothelial cells, suggesting that BSG expression in the vasculature may explain the heightened risk for severe disease with age.
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