Evidence map›Paper›PMID 39320019›Full record

ArticlePharmacology research & perspectives2024

The epsilon toxin from Clostridium perfringens stimulates calcium-activated chloride channels, generating extracellular vesicles in Xenopus oocytes.

Mercè Cases, Jonatan Dorca-Arévalo, Marta Blanch, Sergi Rodil, Beatrice Terni, Mireia Martín-Satué, Artur Llobet, Juan Blasi, Carles Solsona

Abstract read
In one paragraph

Article in Pharmacology research & perspectives, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Epsilon Toxin fromToxins · 2024
    Article
  2. 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

9 authors.

Mercè CasesDepartment of Pathology and Experimental Therapeutics, Faculty of Medicine and Health Sciences-Campus Bellvitge, University of Barcelona, Barcelona, Spain.ORCID 0000-0003-2525-5475
Jonatan Dorca-ArévaloDepartment of Pathology and Experimental Therapeutics, Faculty of Medicine and Health Sciences-Campus Bellvitge, University of Barcelona, Barcelona, Spain.ORCID 0000-0001-7606-0462
Marta BlanchDepartment of Pathology and Experimental Therapeutics, Faculty of Medicine and Health Sciences-Campus Bellvitge, University of Barcelona, Barcelona, Spain.ORCID 0000-0003-1913-0158
Sergi RodilDepartment of Pathology and Experimental Therapeutics, Faculty of Medicine and Health Sciences-Campus Bellvitge, University of Barcelona, Barcelona, Spain.ORCID 0000-0002-0277-6158
Beatrice TerniDepartment of Pathology and Experimental Therapeutics, Faculty of Medicine and Health Sciences-Campus Bellvitge, University of Barcelona, Barcelona, Spain.ORCID 0000-0001-9548-1625
Mireia Martín-SatuéDepartment of Pathology and Experimental Therapeutics, Faculty of Medicine and Health Sciences-Campus Bellvitge, University of Barcelona, Barcelona, Spain.ORCID 0000-0002-9718-4664
Artur LlobetDepartment of Pathology and Experimental Therapeutics, Faculty of Medicine and Health Sciences-Campus Bellvitge, University of Barcelona, Barcelona, Spain.ORCID 0000-0001-5797-6782
Juan BlasiDepartment of Pathology and Experimental Therapeutics, Faculty of Medicine and Health Sciences-Campus Bellvitge, University of Barcelona, Barcelona, Spain.ORCID 0000-0002-0482-9444
Carles SolsonaDepartment of Pathology and Experimental Therapeutics, Faculty of Medicine and Health Sciences-Campus Bellvitge, University of Barcelona, Barcelona, Spain.ORCID 0000-0002-9897-0667

Funding

Centres de Recerca de Catalunya MCIN/AEI/10.13039/501100011033Centres de Recerca de Catalunya PID2021-126677NB-I00Centres de Recerca de Catalunya SAF2017-85818-RCentres de Recerca de Catalunya SGR: 2021 SGR 01075European Regional Development Fund
6 · The paper itself

Abstract

The epsilon toxin (Etx) from Clostridium perfringens has been identified as a potential trigger of multiple sclerosis, functioning as a pore-forming toxin that selectively targets cells expressing the plasma membrane (PM) myelin and lymphocyte protein (MAL). Previously, we observed that Etx induces the release of intracellular ATP in sensitive cell lines. Here, we aimed to re-examine the mechanism of action of the toxin and investigate the connection between pore formation and ATP release. We examined the impact of Etx on Xenopus laevis oocytes expressing human MAL. Extracellular ATP was assessed using the luciferin-luciferase reaction. Activation of calcium-activated chloride channels (CaCCs) and a decrease in the PM surface were recorded using the two-electrode voltage-clamp technique. To evaluate intracellular Ca

Indexed as

Adenosine TriphosphateBacterial ToxinsCalciumChloride ChannelsExtracellular VesiclesOocytesXenopus laevisAnimalsCell MembraneClostridium perfringensFemaleHumansMyelin and Lymphocyte-Associated Proteolipid ProteinsPhospholipid Transfer ProteinsAdenosine TriphosphateBacterial ToxinsCalciumChloride ChannelsClostridium perfringens epsilon-toxinMyelin and Lymphocyte-Associated Proteolipid ProteinsPhospholipid Transfer Proteinscalcium‐activated chloride channelsepsilon toxinextracellular vesiclespore‐forming toxinsscramblaseTMEM16AXenopus laevis oocytes

Identifiers

PMID39320019
PMCPMC11423345

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Registered trials

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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.