Evidence map›Paper›PMID 21878647›Full record

ArticleThe Journal of biological chemistry2011

Staphylococcus aureus protein A mediates invasion across airway epithelial cells through activation of RhoA GTPase signaling and proteolytic activity.

Grace Soong, Francis J Martin, Jarin Chun, Taylor S Cohen, Danielle S Ahn, Alice Prince

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

42 citing papers in PubMed, 70 citations in OpenAlex.

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  11. A Narrative Review on the Role ofOpen forum infectious diseases · 2021
    Review
  12. Review
  13. Review
  14. Interaction ofACS infectious diseases · 2020
    Article
  15. Article
  16. Review
  17. Review
  18. Frontiers in cellular and infection microbiology · 2019
    Review
  19. Article
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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

6 authors at 1 institution in 1 country.

Grace SoongDepartment of Pediatrics, College of Physicians and Surgeons Columbia University, New York, New York 10032.
Francis J MartinDepartment of Pharmacology, College of Physicians and Surgeons Columbia University, New York, New York 10032.
Jarin ChunDepartment of Pharmacology, College of Physicians and Surgeons Columbia University, New York, New York 10032.
Taylor S CohenDepartment of Pediatrics, College of Physicians and Surgeons Columbia University, New York, New York 10032.
Danielle S AhnDepartment of Pediatrics, College of Physicians and Surgeons Columbia University, New York, New York 10032.
Alice PrinceDepartment of Pediatrics, College of Physicians and Surgeons Columbia University, New York, New York 10032; Department of Pharmacology, College of Physicians and Surgeons Columbia University, New York, New York 10032. Electronic address: asp7@columbia.edu.
Columbia University · US

Funding

STAPHYLOCOCCUS AUREUS ACTIVATION OF TNF SIGNALING PATHWAYSR01HL079395 · NHLBI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI PRINCE, ALICE S · 2006 to 2016
$4.3M
NHLBI NIH HHS R01 HL079395
6 · The paper itself

Abstract

Staphyococcus aureus and especially the epidemic methicillin-resistant S. aureus strains cause severe necrotizing pneumonia. The mechanisms whereby these organisms invade across the mucosal epithelial barrier to initiate invasive infection are not well understood. Protein A (SpA), a highly conserved and abundant surface protein of S. aureus, activates TNF receptor 1 and EGF receptor (EGFR) signaling cascades that can perturb the cytoskeleton. We demonstrate that wild-type S. aureus, but not spa mutants, invade across polarized airway epithelial cell monolayers via the paracellular junctions. SpA stimulated a RhoA/ROCK/MLC cascade, resulting in the contraction of the cytoskeleton. SpA(+) but not SpA(-) mutants stimulated activation of EGFR and along with subsequent calpain activity cleaved the membrane-spanning junctional proteins occludin and E-cadherin, facilitating staphylococcal transmigration through the cell-cell junctions. Treatment of polarized human airway epithelial monolayers with inhibitors of ROCK, EGFR, MAPKs, or calpain prevented staphylococcal penetration through the monolayers. In vivo, blocking calpain activity impeded bacterial invasion into the lung parenchyma. Thus, S. aureus exploits multiple receptors available on the airway mucosal surface to facilitate invasion across epithelial barriers.

Indexed as

Signal TransductionAnimalsCadherinsCalpainCell LineErbB ReceptorsFemaleHumansIntercellular JunctionsMiceMutationPneumonia, StaphylococcalProtease InhibitorsProtein Kinase InhibitorsReceptors, Tumor Necrosis Factor, Type IRespiratory MucosaCadherinsCalpainEGFR protein, humanEGFR protein, mouseErbB ReceptorsProtease InhibitorsProtein Kinase InhibitorsReceptors, Tumor Necrosis Factor, Type IrhoA GTP-Binding ProteinRHOA protein, humanRhoA protein, mouserho-Associated Kinasesrho GTP-Binding ProteinsStaphylococcal Protein ATnfrsf1a protein, mouse

Identifiers

PMID21878647
PMCPMC3195615
OpenAlexW2046228858

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.