SARS-CoV-2 Receptor ACE2 Is an Interferon-Stimulated Gene in Human Airway Epithelial Cells and Is Detected in Specific Cell Subsets across Tissues.
Adolescent
Alveolar Epithelial Cells
/ immunology
Angiotensin-Converting Enzyme 2
Animals
Betacoronavirus
/ physiology
COVID-19
Cell Line
Cells, Cultured
Child
Coronavirus Infections
/ virology
Enterocytes
/ immunology
Goblet Cells
/ immunology
HIV Infections
/ immunology
Humans
Influenza, Human
/ immunology
Interferon Type I
/ immunology
Lung
/ cytology
Macaca mulatta
Mice
Mycobacterium tuberculosis
Nasal Mucosa
/ cytology
Pandemics
Peptidyl-Dipeptidase A
/ genetics
Pneumonia, Viral
/ virology
Receptors, Virus
/ genetics
SARS-CoV-2
Serine Endopeptidases
/ metabolism
Single-Cell Analysis
Tuberculosis
/ immunology
Up-Regulation
ACE2
COVID-19
ISG
SARS-CoV-2
human
influenza
interferon
mouse
non-human primate
scRNA-seq
Journal
Cell
ISSN: 1097-4172
Titre abrégé: Cell
Pays: United States
ID NLM: 0413066
Informations de publication
Date de publication:
28 05 2020
28 05 2020
Historique:
received:
13
03
2020
revised:
03
04
2020
accepted:
20
04
2020
pubmed:
16
5
2020
medline:
6
6
2020
entrez:
16
5
2020
Statut:
ppublish
Résumé
There is pressing urgency to understand the pathogenesis of the severe acute respiratory syndrome coronavirus clade 2 (SARS-CoV-2), which causes the disease COVID-19. SARS-CoV-2 spike (S) protein binds angiotensin-converting enzyme 2 (ACE2), and in concert with host proteases, principally transmembrane serine protease 2 (TMPRSS2), promotes cellular entry. The cell subsets targeted by SARS-CoV-2 in host tissues and the factors that regulate ACE2 expression remain unknown. Here, we leverage human, non-human primate, and mouse single-cell RNA-sequencing (scRNA-seq) datasets across health and disease to uncover putative targets of SARS-CoV-2 among tissue-resident cell subsets. We identify ACE2 and TMPRSS2 co-expressing cells within lung type II pneumocytes, ileal absorptive enterocytes, and nasal goblet secretory cells. Strikingly, we discovered that ACE2 is a human interferon-stimulated gene (ISG) in vitro using airway epithelial cells and extend our findings to in vivo viral infections. Our data suggest that SARS-CoV-2 could exploit species-specific interferon-driven upregulation of ACE2, a tissue-protective mediator during lung injury, to enhance infection.
Identifiants
pubmed: 32413319
pii: S0092-8674(20)30500-6
doi: 10.1016/j.cell.2020.04.035
pmc: PMC7252096
pii:
doi:
Substances chimiques
Interferon Type I
0
Receptors, Virus
0
Peptidyl-Dipeptidase A
EC 3.4.15.1
ACE2 protein, human
EC 3.4.17.23
Ace2 protein, mouse
EC 3.4.17.23
Angiotensin-Converting Enzyme 2
EC 3.4.17.23
Serine Endopeptidases
EC 3.4.21.-
TMPRSS2 protein, human
EC 3.4.21.-
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
1016-1035.e19Subventions
Organisme : NHLBI NIH HHS
ID : R01 HL128241
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL095791
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL118185
Pays : United States
Organisme : NHLBI NIH HHS
ID : K08 HL130595
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL117945
Pays : United States
Organisme : NIAID NIH HHS
ID : R33 AI116184
Pays : United States
Organisme : NIAID NIH HHS
ID : U19 AI095219
Pays : United States
Organisme : NIAID NIH HHS
ID : U19 AI057229
Pays : United States
Organisme : Medical Research Council
ID : MR/R006237/1
Pays : United Kingdom
Organisme : NIDA NIH HHS
ID : DP2 DA042422
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI126623
Pays : United States
Organisme : NIGMS NIH HHS
ID : R01 GM081871
Pays : United States
Organisme : NHLBI NIH HHS
ID : U19 HL129902
Pays : United States
Organisme : Medical Research Council
ID : MR/S005579/1
Pays : United Kingdom
Organisme : NIAID NIH HHS
ID : R37 AI052353
Pays : United States
Organisme : NHLBI NIH HHS
ID : K12 HL143886
Pays : United States
Organisme : Medical Research Council
ID : MR/S035907/1
Pays : United Kingdom
Organisme : NIAID NIH HHS
ID : K23 AI139352
Pays : United States
Organisme : Medical Research Council
ID : MR/S036334/1
Pays : United Kingdom
Organisme : NHLBI NIH HHS
ID : R01 HL145372
Pays : United States
Organisme : NIGMS NIH HHS
ID : T32 GM007753
Pays : United States
Organisme : NIAID NIH HHS
ID : U19 AI051731
Pays : United States
Organisme : NHLBI NIH HHS
ID : K08 HL146943
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI078908
Pays : United States
Organisme : Medical Research Council
ID : MR/K017047/1
Pays : United Kingdom
Organisme : NIDDK NIH HHS
ID : P30 DK034854
Pays : United States
Organisme : NIGMS NIH HHS
ID : T32 GM087237
Pays : United States
Organisme : NHLBI NIH HHS
ID : K23 HL111113
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL136209
Pays : United States
Organisme : Medical Research Council
ID : MR/P009581/1
Pays : United Kingdom
Organisme : NIAID NIH HHS
ID : R01 AI124378
Pays : United States
Organisme : NIAID NIH HHS
ID : U24 AI118672
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI136041
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI126617
Pays : United States
Organisme : NHLBI NIH HHS
ID : P01 HL132821
Pays : United States
Organisme : NIAID NIH HHS
ID : R56 AI139053
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI137057
Pays : United States
Organisme : Medical Research Council
ID : MR/R015635/1
Pays : United Kingdom
Investigateurs
Nicholas Banovich
(N)
Pascal Barbry
(P)
Alvis Brazma
(A)
Tushar Desai
(T)
Thu Elizabeth Duong
(TE)
Oliver Eickelberg
(O)
Christine Falk
(C)
Michael Farzan
(M)
Ian Glass
(I)
Muzlifah Haniffa
(M)
Peter Horvath
(P)
Deborah Hung
(D)
Naftali Kaminski
(N)
Mark Krasnow
(M)
Jonathan A Kropski
(JA)
Malte Kuhnemund
(M)
Robert Lafyatis
(R)
Haeock Lee
(H)
Sylvie Leroy
(S)
Sten Linnarson
(S)
Joakim Lundeberg
(J)
Kerstin Meyer
(K)
Alexander Misharin
(A)
Martijn Nawijn
(M)
Marko Z Nikolic
(MZ)
Jose Ordovas-Montanes
(J)
Dana Pe'er
(D)
Joseph Powell
(J)
Stephen Quake
(S)
Jay Rajagopal
(J)
Purushothama Rao Tata
(PR)
Emma L Rawlins
(EL)
Aviv Regev
(A)
Paul A Reyfman
(PA)
Mauricio Rojas
(M)
Orit Rosen
(O)
Kourosh Saeb-Parsy
(K)
Christos Samakovlis
(C)
Herbert Schiller
(H)
Joachim L Schultze
(JL)
Max A Seibold
(MA)
Alex K Shalek
(AK)
Douglas Shepherd
(D)
Jason Spence
(J)
Avrum Spira
(A)
Xin Sun
(X)
Sarah Teichmann
(S)
Fabian Theis
(F)
Alexander Tsankov
(A)
Maarten van den Berge
(M)
Michael von Papen
(M)
Jeffrey Whitsett
(J)
Ramnik Xavier
(R)
Yan Xu
(Y)
Laure-Emmanuelle Zaragosi
(LE)
Kun Zhang
(K)
Informations de copyright
Copyright © 2020 The Authors. Published by Elsevier Inc. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of Interests A.R. is an SAB member of ThermoFisher Scientific, Neogene Therapeutics, Asimov, and Syros Pharmaceuticals; a co-founder of and equity holder in Celsius Therapeutics; and an equity holder in Immunitas Therapeutics. A.K.S. reports compensation for consulting and/or SAB membership from Merck, Honeycomb Biotechnologies, Cellarity, Cogen Therapeutics, Orche Bio, and Dahlia Biosciences. L.S.K. is on the SAB for HiFiBio; she reports research funding from Kymab Limited, Bristol Meyers Squibb, Magenta Therapeutics, BlueBird Bio, and Regeneron Pharmaceuticals and consulting fees from Equillium, FortySeven, Inc, Novartis, Inc, EMD Serono, Gilead Sciences, and Takeda Pharmaceuticals. A.S. is an employee of Johnson and Johnson. N.K. is an inventor on a patent using thyroid hormone mimetics in acute lung injury that is now being considered for intervention in COVID-19 patients. J.L. is a scientific consultant for 10X Genomics, Inc. O.R.R, is a co-inventor on patent applications filed by the Broad Institute to inventions relating to single-cell genomics applications, such as in PCT/US2018/060860 and US Provisional Application No. 62/745,259. S.T. in the last three years was a consultant at Genentech, Biogen, and Roche and is a member of the SAB of Foresite Labs. M.H.W. is now an employee of Pfizer. F.J.T. reports receiving consulting fees from Roche Diagnostics GmbH and ownership interest in Cellarity, Inc. P.H. is a co-inventor on a patent using artificial intelligence and high-resolution microscopy for COVID-19 infection testing based on serology.
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