Evidence map›Paper›PMID 33434105›Full record

ArticleAmerican journal of physiology. Lung cellular and molecular physiology2021

SARS-CoV-2 may hijack GPCR signaling pathways to dysregulate lung ion and fluid transport.

Reem Abdel Hameid, Estelle Cormet-Boyaka, Wolfgang M Kuebler, Mohammed Uddin, Bakhrom K Berdiev

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Lung cellular and molecular physiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
8.4field-weighted citation impact, top 2% 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

33 citing papers in PubMed, 62 citations in OpenAlex.

  1. Article
  2. Review
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  4. Functional CFTR may be required for Prevotella melaninogenica regulation of epithelial cell defense against Staphylococcus aureus.Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society · 2026
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  8. Mechanisms by which the cystic fibrosis transmembrane conductance regulator may influence SARS-CoV-2 infection and COVID-19 disease severity.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2023
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  11. Fibrinolytic system and COVID-19: From an innovative view of epithelial ion transport.Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie · 2023
    Review
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  14. Article
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  17. Early reduction of SARS-CoV-2-replication in bronchial epithelium by kinin BJournal of molecular medicine (Berlin, Germany) · 2022
    Article
  18. Article
  19. A year in review: Real world evidence, functional monitoring and emerging therapeutics in 2021.Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society · 2022
    Review
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 4 institutions in 4 countries.

Reem Abdel HameidMohammed Bin Rashid University of Medicine and Health Sciences, Dubai, United Arab Emirates.
Estelle Cormet-BoyakaDivision of Veterinary Biosciences, The Ohio State University, Columbus, Ohio.
Wolfgang M KueblerInstitute of Physiology, Charité-Universitätsmedizin Berlin, Berlin, Germany.
Mohammed UddinMohammed Bin Rashid University of Medicine and Health Sciences, Dubai, United Arab Emirates.
Bakhrom K BerdievMohammed Bin Rashid University of Medicine and Health Sciences, Dubai, United Arab Emirates.
Mohammed Bin Rashid University of Medicine and Health Sciences · AECharité - Universitätsmedizin Berlin · DEHospital for Sick Children · CAThe Ohio State University · US

Funding

ANDROGEN REGULATION OF HUMAN SEBACEOUS GLANDSK08AR002018 · NIAMS · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI THIBOUTOT, DIANE M. · 1997 to 2001
$225k
Al Jalila Foundation Award AJF201763AlMahmeed Collaborative Research Award 2018 ALM1801MBRU-COM Internal Grant Award MBRU-CM-RG2018-04MBRU-COM Internal Grant Award MBRU-CM-RG2018-05Sandoq Al Watan Research & Development Grant SWARD-F2018-002
6 · The paper itself

Abstract

The tropism of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), a virus responsible for the ongoing coronavirus disease 2019 (COVID-19) pandemic, toward the host cells is determined, at least in part, by the expression and distribution of its cell surface receptor, angiotensin-converting enzyme 2 (ACE2). The virus further exploits the host cellular machinery to gain access into the cells; its spike protein is cleaved by a host cell surface transmembrane serine protease 2 (TMPRSS2) shortly after binding ACE2, followed by its proteolytic activation at a furin cleavage site. The virus primarily targets the epithelium of the respiratory tract, which is covered by a tightly regulated airway surface liquid (ASL) layer that serves as a primary defense mechanism against respiratory pathogens. The volume and viscosity of this fluid layer is regulated and maintained by a coordinated function of different transport pathways in the respiratory epithelium. We argue that SARS-CoV-2 may potentially alter evolutionary conserved second-messenger signaling cascades via activation of G protein-coupled receptors (GPCRs) or by directly modulating G protein signaling. Such signaling may in turn adversely modulate transepithelial transport processes, especially those involving cystic fibrosis transmembrane conductance regulator (CFTR) and epithelial Na

Indexed as

Biological TransportCOVID-19HumansLungReceptors, G-Protein-CoupledSARS-CoV-2Signal TransductionReceptors, G-Protein-CoupledCFTRCOVID-19ENaCGPCRSARS-CoV-2

Identifiers

PMID33434105
PMCPMC7938641
OpenAlexW3120587241

What OpenQuestion holds

Textmetadata
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.