Evidence map›Paper›PMID 34960806›Full record

ArticleViruses2021

Differential Effect of SARS-CoV-2 Spike Glycoprotein 1 on Human Bronchial and Alveolar Lung Mucosa Models: Implications for Pathogenicity.

Mizanur Rahman, Martin Irmler, Sandeep Keshavan, Micol Introna, Johannes Beckers, Lena Palmberg, Gunnar Johanson, Koustav Ganguly, Swapna Upadhyay

Open access · goldAbstract read
In one paragraph

Article in Viruses, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
3.3field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

18 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Potential relationships between circulating gene expression ofJournal of Zhejiang University. Science. B · 2025
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 3 countries.

Mizanur RahmanUnit of Integrative Toxicology, Institute of Environmental Medicine, Karolinska Institutet, 17 177 Stockholm, Sweden.
Martin IrmlerInstitute of Experimental Genetics, Helmholtz Zentrum München GmbH, 85764 Neuherberg, Germany.
Sandeep KeshavanAdolphe Merkle Institute, University of Fribourg, Chemin des Verdiers 4, 1700 Fribourg, Switzerland.ORCID 0000-0002-2403-4083
Micol IntronaUnit of Integrative Toxicology, Institute of Environmental Medicine, Karolinska Institutet, 17 177 Stockholm, Sweden.ORCID 0000-0002-5564-1994
Johannes BeckersInstitute of Experimental Genetics, Helmholtz Zentrum München GmbH, 85764 Neuherberg, Germany.ORCID 0000-0002-1038-7160
Lena PalmbergUnit of Integrative Toxicology, Institute of Environmental Medicine, Karolinska Institutet, 17 177 Stockholm, Sweden.
Gunnar JohansonUnit of Integrative Toxicology, Institute of Environmental Medicine, Karolinska Institutet, 17 177 Stockholm, Sweden.ORCID 0000-0002-8759-9567
Koustav GangulyUnit of Integrative Toxicology, Institute of Environmental Medicine, Karolinska Institutet, 17 177 Stockholm, Sweden.ORCID 0000-0001-8531-8154
Swapna UpadhyayUnit of Integrative Toxicology, Institute of Environmental Medicine, Karolinska Institutet, 17 177 Stockholm, Sweden.
Karolinska Institutet · SEHelmholtz Zentrum München · DEUniversity of Fribourg · CH

Funding

IMM strategic grant SU-COVID (2020-2021)Swedish Heart Lung Foundation (KG: 20200776)Swedish Research Council LP: 2018-03233
6 · The paper itself

Abstract

backgroundThe SARS-CoV-2 spike protein mediates attachment of the virus to the host cell receptor and fusion between the virus and the cell membrane. The S1 subunit of the spike glycoprotein (S1 protein) contains the angiotensin converting enzyme 2 (ACE2) receptor binding domain. The SARS-CoV-2 variants of concern contain mutations in the S1 subunit. The spike protein is the primary target of neutralizing antibodies generated following infection, and constitutes the viral component of mRNA-based COVID-19 vaccines.

methodsTherefore, in this work we assessed the effect of exposure (24 h) to 10 nM SARS-CoV-2 recombinant S1 protein on physiologically relevant human bronchial (bro) and alveolar (alv) lung mucosa models cultured at air-liquid interface (ALI) (

resultsExposure to S1 protein induced the surface expression of ACE2, toll like receptor (TLR) 2, and TLR4 in both bro-ALI and alv-ALI models. Transcript expression analysis identified 117 (bro-ALI) and 97 (alv-ALI) differentially regulated genes (

conclusionsIn conclusion, we observed a typical anti-viral response in the bronchial model and a pro-fibrotic response in the alveolar model. The bro-ALI and alv-ALI models may serve as an easy and robust platform for assessing the pathogenicity of SARS-CoV-2 variants of concern at different lung regions.

Indexed as

Angiotensin-Converting Enzyme 2BronchiCytokinesGene Expression ProfilingHumansLungModels, BiologicalProtein Interaction Domains and MotifsRecombinant ProteinsRespiratory MucosaSARS-CoV-2Spike Glycoprotein, CoronavirusToll-Like Receptor 2Toll-Like Receptor 4ACE2 protein, humanAngiotensin-Converting Enzyme 2CytokinesRecombinant ProteinsSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2TLR2 protein, humanTLR4 protein, humanToll-Like Receptor 2Toll-Like Receptor 4coronavirusCOVID-19fibrosislungMERS (middle east respiratory syndrome)pulmonarySARS-CoV-2SARS (severe acute respiratory syndrome)spike protein

Identifiers

PMID34960806
PMCPMC8708014
OpenAlexW4200272017

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.