Your browser doesn't support javascript.
loading
Cardiorenal Tissues Express SARS-CoV-2 Entry Genes and Basigin (BSG/CD147) Increases With Age in Endothelial Cells.
Ahmetaj-Shala, Blerina; Vaja, Ricky; Atanur, Santosh S; George, Peter M; Kirkby, Nicholas S; Mitchell, Jane A.
Afiliação
  • Ahmetaj-Shala B; Cardiorespiratory Interface, National Heart and Lung Institute, Imperial College London, London, United Kingdom.
  • Vaja R; Cardiorespiratory Interface, National Heart and Lung Institute, Imperial College London, London, United Kingdom.
  • Atanur SS; Department of Metabolism, Digestion and Reproduction, Faculty of Medicine, Imperial College London, London, United Kingdom.
  • George PM; Institute of Translational Medicine and Therapeutics, Data Science Group, National Institute for Health Research, Biomedical Research Centre, Imperial College London, London, United Kingdom.
  • Kirkby NS; Cardiorespiratory Interface, National Heart and Lung Institute, Imperial College London, London, United Kingdom.
  • Mitchell JA; Interstitial Lung Disease Unit, National Heart and Lung Institute, Imperial College London, Royal Brompton and Harefield NHS Foundation Trust, London, United Kingdom.
JACC Basic Transl Sci ; 5(11): 1111-1123, 2020 Nov.
Article em En | MEDLINE | ID: mdl-33073064
ABSTRACT
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.
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Ano de publicação: 2020 Tipo de documento: Article