Evidence map›Paper›PMID 27613716›Full record

ArticleToxicological sciences : an official journal of the Society of Toxicology2016

Transient Proteotoxicity of Bacterial Virulence Factor Pyocyanin in Renal Tubular Epithelial Cells Induces ER-Related Vacuolation and Can Be Efficiently Modulated by Iron Chelators.

Valeri V Mossine, James K Waters, Deborah L Chance, Thomas P Mawhinney

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in Toxicological sciences : an official journal of the Society of Toxicology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.6field-weighted citation impact, top 27% 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

12 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Advances inMicroorganisms · 2025
    Review
  3. Paraptosis-A Distinct Pathway to Cell Death.International journal of molecular sciences · 2024
    Review
  4. Article
  5. Article
  6. Structural and Functional Studies ofMolecules (Basel, Switzerland) · 2022
    Article
  7. Review
  8. Article
  9. Structure, Antioxidant and Anti-inflammatory Activities of the (4Pharmaceuticals (Basel, Switzerland) · 2020
    Article
  10. Review
  11. Intra-molecular 1,5-S⋯N σ-hole inter-action in (Acta crystallographica. Section E, Crystallographic communications · 2020
    Article
  12. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 2 countries.

Valeri V MossineDepartment of Biochemistry mossinev@missouri.edu.
James K WatersExperiment Station Chemical Labs, University of Missouri, Columbia, Missouri 65211.
Deborah L ChanceDepartment of Molecular Microbiology and Immunology.
Thomas P MawhinneyDepartment of Biochemistry.
University of Missouri · USBipar · FR

Funding

The Interactions Core/Mark McintoshP50AT006273 · NCCIH · UNIVERSITY OF MISSOURI-COLUMBIA · PI LUBAHN, DENNIS B · 2010 to 2014
$7.4M
NCCIH NIH HHS P50 AT006273
6 · The paper itself

Abstract

Persistent infections of biofilm forming bacteria, such as Pseudomonas aeruginosa, are common among human populations, due to the bacterial resistance to antibiotics and other adaptation strategies, including release of cytotoxic virulent factors such as pigment pyocyanin (PCN). Urinary tract infections harbor P. aeruginosa strains characterized by the highest PCN-producing capacity, yet no information is available on PCN cytotoxicity mechanism in kidney. We report here that renal tubular epithelial cell (RTEC) line NRK-52E responds to PCN treatments with paraptosis-like activity features. Specifically, PCN-treated cells experienced dilation of endoplasmic reticulum (ER) and an extensive development of ER-derived vacuoles after about 8 h. This process was accompanied with hyper-activation of proteotoxic stress-inducible transcription factors Nrf2, ATF6, and HSF-1. The cells could be rescued by withdrawal of PCN from the culture media before the vacuoles burst and cells die of non-programmed necrosis after about 24-30 h. The paraptosis-like activity was abrogated by co-treatment of the cells with metal-chelating antioxidants. A microscopic examination of cells co-treated with PCN and agents aiming at a variety of the cellular stress mediators and pathways have identified iron as a single most significant co-factor of the PCN cytotoxicity in the RTECs. Among biologically relevant metal ions, low micromolar Fe

Indexed as

Activating Transcription Factor 6AnimalsCell LineCell ProliferationDose-Response Relationship, DrugEndoplasmic ReticulumEpithelial CellsGlutathioneHeat Shock Transcription FactorsIronIron Chelating AgentsKidney TubulesNecrosisNF-E2-Related Factor 2Oxidative StressPseudomonas aeruginosaActivating Transcription Factor 6ATF6 protein, humanGlutathioneHeat Shock Transcription FactorsHSF1 protein, humanIronIron Chelating AgentsNFE2L2 protein, humanNF-E2-Related Factor 2Pyocyanineendoplasmic reticulum stress.glutathioneironproteotoxic stress responsePyocyaninrenal tubular epithelial cells

Identifiers

PMID27613716
PMCPMC5139071
OpenAlexW2511099113

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.