Evidence map›Paper›PMID 35154132›Full record

ArticleFrontiers in immunology2022

Oxysterols Protect Epithelial Cells Against Pore-Forming Toxins.

Thomas J R Ormsby, Sian E Owens, Liam Clement, Tom J Mills, James G Cronin, John J Bromfield, Iain Martin Sheldon

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

7 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. mBio · 2025
    Article
  4. Oxysterols in Infectious Diseases.Advances in experimental medicine and biology · 2024
    Article
  5. Article
  6. Article
  7. Review
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

7 authors at 2 institutions in 2 countries.

Thomas J R OrmsbySwansea University Medical School, Swansea University, Swansea, United Kingdom.
Sian E OwensSwansea University Medical School, Swansea University, Swansea, United Kingdom.
Liam ClementSwansea University Medical School, Swansea University, Swansea, United Kingdom.
Tom J MillsSwansea University Medical School, Swansea University, Swansea, United Kingdom.
James G CroninSwansea University Medical School, Swansea University, Swansea, United Kingdom.
John J BromfieldDepartment of Animal Sciences, University of Florida, Gainesville, FL, United States.
Iain Martin SheldonSwansea University Medical School, Swansea University, Swansea, United Kingdom.
Swansea University · GBUniversity of Florida · US

Funding

Uterine infection and infertility: how microbial infection of the reproductive tract causes ovarian dysfunction.R01HD084316 · NICHD · UNIVERSITY OF FLORIDA · PI BROMFIELD, JOHN J · 2016 to 2020
$1.7M
NICHD NIH HHS R01 HD084316
6 · The paper itself

Abstract

Many species of bacteria produce toxins such as cholesterol-dependent cytolysins that form pores in cell membranes. Membrane pores facilitate infection by releasing nutrients, delivering virulence factors, and causing lytic cell damage - cytolysis. Oxysterols are oxidized forms of cholesterol that regulate cellular cholesterol and alter immune responses to bacteria. Whether oxysterols also influence the protection of cells against pore-forming toxins is unresolved. Here we tested the hypothesis that oxysterols stimulate the intrinsic protection of epithelial cells against damage caused by cholesterol-dependent cytolysins. We treated epithelial cells with oxysterols and then challenged them with the cholesterol-dependent cytolysin, pyolysin. Treating HeLa cells with 27-hydroxycholesterol, 25-hydroxycholesterol, 7α-hydroxycholesterol, or 7β-hydroxycholesterol reduced pyolysin-induced leakage of lactate dehydrogenase and reduced pyolysin-induced cytolysis. Specifically, treatment with 10 ng/ml 27-hydroxycholesterol for 24 h reduced pyolysin-induced lactate dehydrogenase leakage by 88%, and reduced cytolysis from 74% to 1%. Treating HeLa cells with 27-hydroxycholesterol also reduced pyolysin-induced leakage of potassium ions, prevented mitogen-activated protein kinase cell stress responses, and limited alterations in the cytoskeleton. Furthermore, 27-hydroxycholesterol reduced pyolysin-induced damage in lung and liver epithelial cells, and protected against the cytolysins streptolysin O and

Indexed as

BacteriaBacterial ProteinsBacterial ToxinsEpithelial CellsHeLa CellsHemolysin ProteinsHumansOxysterolsVirulence FactorsBacterial ProteinsBacterial ToxinsHemolysin ProteinsOxysterolsPyolysin, Arcanobacterium pyogenesVirulence Factorscholesterolcholesterol-dependent cytolysincytoprotectionepithelial cellsliver X receptoroxysterolpore-forming toxins

Identifiers

PMID35154132
PMCPMC8825411
OpenAlexW4210535426

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.