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Elevated Glucose Levels Favor SARS-CoV-2 Infection and Monocyte Response through a HIF-1α/Glycolysis-Dependent Axis.

Authors :
Codo AC
Davanzo GG
Monteiro LB
de Souza GF
Muraro SP
Virgilio-da-Silva JV
Prodonoff JS
Carregari VC
de Biagi Junior CAO
Crunfli F
Jimenez Restrepo JL
Vendramini PH
Reis-de-Oliveira G
Bispo Dos Santos K
Toledo-Teixeira DA
Parise PL
Martini MC
Marques RE
Carmo HR
Borin A
Coimbra LD
Boldrini VO
Brunetti NS
Vieira AS
Mansour E
Ulaf RG
Bernardes AF
Nunes TA
Ribeiro LC
Palma AC
Agrela MV
Moretti ML
Sposito AC
Pereira FB
Velloso LA
Vinolo MAR
Damasio A
Proença-Módena JL
Carvalho RF
Mori MA
Martins-de-Souza D
Nakaya HI
Farias AS
Moraes-Vieira PM
Source :
Cell metabolism [Cell Metab] 2020 Sep 01; Vol. 32 (3), pp. 437-446.e5. Date of Electronic Publication: 2020 Jul 17.
Publication Year :
2020

Abstract

COVID-19 can result in severe lung injury. It remained to be determined why diabetic individuals with uncontrolled glucose levels are more prone to develop the severe form of COVID-19. The molecular mechanism underlying SARS-CoV-2 infection and what determines the onset of the cytokine storm found in severe COVID-19 patients are unknown. Monocytes and macrophages are the most enriched immune cell types in the lungs of COVID-19 patients and appear to have a central role in the pathogenicity of the disease. These cells adapt their metabolism upon infection and become highly glycolytic, which facilitates SARS-CoV-2 replication. The infection triggers mitochondrial ROS production, which induces stabilization of hypoxia-inducible factor-1α (HIF-1α) and consequently promotes glycolysis. HIF-1α-induced changes in monocyte metabolism by SARS-CoV-2 infection directly inhibit T cell response and reduce epithelial cell survival. Targeting HIF-1ɑ may have great therapeutic potential for the development of novel drugs to treat COVID-19.<br />Competing Interests: Declaration of Interests Authors declare no competing interests.<br /> (Copyright © 2020 Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1932-7420
Volume :
32
Issue :
3
Database :
MEDLINE
Journal :
Cell metabolism
Publication Type :
Academic Journal
Accession number :
32697943
Full Text :
https://doi.org/10.1016/j.cmet.2020.07.007