Evidence map›Paper›PMID 38607044›Full record

ArticleCells2024

Extracellular Vesicles of Patients on Peritoneal Dialysis Inhibit the TGF-β- and PDGF-B-Mediated Fibrotic Processes.

Beáta Szebeni, Apor Veres-Székely, Domonkos Pap, Péter Bokrossy, Zoltán Varga, Anikó Gaál, Judith Mihály, Éva Pállinger, István M Takács, Csenge Pajtók and 4 more

Open access · goldAbstract read
In one paragraph

Article in Cells, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
0.9field-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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 4 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Anti-fibrotic effect ofFrontiers in bioengineering and biotechnology · 2026
    Article
  5. Article
  6. Roles of PDGF/PDGFR signaling in various organs.The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology · 2025
    Review
  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

14 authors at 2 institutions in 1 country.

Beáta SzebeniPediatric Center, MTA Center of Excellence, Semmelweis University, 1083 Budapest, Hungary.
Apor Veres-SzékelyPediatric Center, MTA Center of Excellence, Semmelweis University, 1083 Budapest, Hungary.ORCID 0000-0002-6830-8779
Domonkos PapPediatric Center, MTA Center of Excellence, Semmelweis University, 1083 Budapest, Hungary.ORCID 0000-0002-1718-1210
Péter BokrossyPediatric Center, MTA Center of Excellence, Semmelweis University, 1083 Budapest, Hungary.
Zoltán VargaTTK Biological Nanochemistry Research Group, Institute of Materials and Environmental Chemistry, Research Centre for Natural Sciences, 1117 Budapest, Hungary.ORCID 0000-0002-5741-2669
Anikó GaálTTK Biological Nanochemistry Research Group, Institute of Materials and Environmental Chemistry, Research Centre for Natural Sciences, 1117 Budapest, Hungary.
Judith MihályTTK Biological Nanochemistry Research Group, Institute of Materials and Environmental Chemistry, Research Centre for Natural Sciences, 1117 Budapest, Hungary.
Éva PállingerDepartment of Genetics, Cell- and Immunobiology, Semmelweis University, 1089 Budapest, Hungary.ORCID 0000-0002-5789-0951
István M TakácsPediatric Center, MTA Center of Excellence, Semmelweis University, 1083 Budapest, Hungary.
Csenge PajtókPediatric Center, MTA Center of Excellence, Semmelweis University, 1083 Budapest, Hungary.ORCID 0000-0001-9685-4868
Mária BernáthPediatric Center, MTA Center of Excellence, Semmelweis University, 1083 Budapest, Hungary.
György S ReuszPediatric Center, MTA Center of Excellence, Semmelweis University, 1083 Budapest, Hungary.
Attila J SzabóPediatric Center, MTA Center of Excellence, Semmelweis University, 1083 Budapest, Hungary.
Ádám VannayPediatric Center, MTA Center of Excellence, Semmelweis University, 1083 Budapest, Hungary.
Semmelweis University · HUInstitute of Materials and Environmental Chemistry · HU

Funding

Hungarian Academic of Sciences, János Bolyai Research Scholarship.Hungarian Research Network ELKH-POC-2022-024National Research, Development and Innovation Office 2020-1-1-2-PIACI-KFI_2020-00021National Research, Development and Innovation Office K-125470National Research, Development and Innovation Office K 131594National Research, Development and Innovation Office K-142728New National Excellence Program of the Ministry for Culture and Innovation from the Source of the National Research, Development and Innovation Fund ÚNKP-23-3-I-SE-36New National Excellence Program of the Ministry for Culture and Innovation from the Source of the National Research, Development and Innovation Fund ÚNKP-23-3-I-SE-42New National Excellence Program of the Ministry for Culture and Innovation from the Source of the National Research, Development and Innovation Fund ÚNKP-23-4-II-SE-29Semmelweis University RRF-2.3.1-21-2022-00003Semmelweis University STIA-KFI-2021Semmelweis University TKP2021-EGA-23Semmelweis University TKP2021-EGA-24the New National Excellence Program of the Ministry for Culture and Innovation from the Source of the National Research, Development and Innovation Fund ÚNKP-23-5-SE-15
6 · The paper itself

Abstract

Among patients on peritoneal dialysis (PD), 50-80% will develop peritoneal fibrosis, and 0.5-4.4% will develop life-threatening encapsulating peritoneal sclerosis (EPS). Here, we investigated the role of extracellular vesicles (EVs) on the TGF-β- and PDGF-B-driven processes of peritoneal fibrosis. EVs were isolated from the peritoneal dialysis effluent (PDE) of children receiving continuous ambulatory PD. The impact of PDE-EVs on the epithelial-mesenchymal transition (EMT) and collagen production of the peritoneal mesothelial cells and fibroblasts were investigated in vitro and in vivo in the chlorhexidine digluconate (CG)-induced mice model of peritoneal fibrosis. PDE-EVs showed spherical morphology in the 100 nm size range, and their spectral features, CD63, and annexin positivity were characteristic of EVs. PDE-EVs penetrated into the peritoneal mesothelial cells and fibroblasts and reduced their PDE- or PDGF-B-induced proliferation. Furthermore, PDE-EVs inhibited the PDE- or TGF-β-induced EMT and collagen production of the investigated cell types. PDE-EVs contributed to the mesothelial layer integrity and decreased the submesothelial thickening of CG-treated mice. We demonstrated that PDE-EVs significantly inhibit the PDGF-B- or TGF-β-induced fibrotic processes in vitro and in vivo, suggesting that EVs may contribute to new therapeutic strategies to treat peritoneal fibrosis and other fibroproliferative diseases.

Indexed as

Extracellular VesiclesPeritoneal DialysisPeritoneal FibrosisAnimalsChildCollagenHumansMicePeritoneumTransforming Growth Factor betaCollagenTransforming Growth Factor betaextracellular vesiclesfibrosismesenchymal transitionperitoneal dialysistherapy

Identifiers

PMID38607044
PMCPMC11011990
OpenAlexW4393353273

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.