Evidence map›Paper›PMID 41261342›Full record

ArticleJournal of cellular and molecular medicine2025

Role of TLR4 in Enteric Glia Response to Clostridioides Difficile Toxins: Insights From In Vivo and In Vitro Studies.

Maria Lucianny Lima Barbosa, Deiziane Viana da Silva Costa, Dvison Melo de Pacífico, Conceição da Silva Martins Rebouças, Cirle Alcantara Warren, Renata Ferreira Carvalho de Leitão, Gerly Anne de Castro Brito

Abstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Article
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.

Maria Lucianny Lima BarbosaCenter for Studies in Microscopy and Image Processing (NEMPI), Department of Morphology, Federal University of Ceará, Fortaleza, Brazil.
Deiziane Viana da Silva CostaDivision of Infectious Diseases and International Health, University of Virginia, Charlottesville, Virginia, USA.ORCID 0000-0001-6402-8908
Dvison Melo de PacíficoCenter for Studies in Microscopy and Image Processing (NEMPI), Department of Morphology, Federal University of Ceará, Fortaleza, Brazil.
Conceição da Silva Martins RebouçasCenter for Studies in Microscopy and Image Processing (NEMPI), Department of Morphology, Federal University of Ceará, Fortaleza, Brazil.
Cirle Alcantara WarrenDivision of Infectious Diseases and International Health, University of Virginia, Charlottesville, Virginia, USA.
Renata Ferreira Carvalho de LeitãoCenter for Studies in Microscopy and Image Processing (NEMPI), Department of Morphology, Federal University of Ceará, Fortaleza, Brazil.ORCID 0000-0003-0202-771X
Gerly Anne de Castro BritoCenter for Studies in Microscopy and Image Processing (NEMPI), Department of Morphology, Federal University of Ceará, Fortaleza, Brazil.

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico 408779/2021-7
6 · The paper itself

Abstract

Clostridioides difficile (C. difficile ) is a Gram-positive anaerobic bacillus that causes intestinal disorders. Toll-like receptor 4 (TLR4) plays a key role in innate immunity. This study examines the role of TLR4 in the response to C. difficile toxins, which induce cell death and inflammatory responses in enteric glial cells (EGCs). Male C57BL/6 mice were infected with C. difficile, and cecum samples were analysed 3 days post-infection for TLR4 expression. In vitro, EGCs were exposed to C. difficile toxins with or without C34, a TLR4 antagonist, or pre-exposed to TLR4-specific 21-nt small interfering RNAs (siRNA). TLR4 expression was assessed by immunocytochemistry, immunofluorescence, qPCR, and Western blotting. NFκB p65, TNF-α, IL-6, cleaved caspase-3, and phosphatidylserine binding to annexin-V were evaluated. TLR4 expression increased in infected intestinal tissue and toxin-exposed EGCs. TLR4 antagonist or TLR4 knockdown reduced NFκB p65 nuclear translocation and TNF-α expression but did not affect IL-6 upregulation. Additionally, TLR4 antagonist or TLR4 knockdown mitigated toxin-induced cell death, as shown by decreased cleaved caspase-3 and phosphatidylserine binding. These findings suggest that TLR4 contributes to C. difficile pathogenesis and that its inhibition reduces inflammation and prevents cell death in EGCs.

Indexed as

Bacterial ToxinsClostridioides difficileClostridium InfectionsNeurogliaToll-Like Receptor 4AnimalsMaleMiceMice, Inbred C57BLTranscription Factor RelATumor Necrosis Factor-alphaBacterial ToxinsTlr4 protein, mouseToll-Like Receptor 4Transcription Factor RelATumor Necrosis Factor-alphaClostridioides difficileClostridium difficileenteric gliatoll‐like receptorstoxins

Identifiers

PMID41261342
PMCPMC12629862

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.