Evidence map›Paper›PMID 35163409›Full record

ArticleInternational journal of molecular sciences2022

Extracellular Vesicles Derived from Human Liver Stem Cells Attenuate Chronic Kidney Disease Development in an In Vivo Experimental Model of Renal Ischemia and Reperfusion Injury.

Stefania Bruno, Giulia Chiabotto, Massimo Cedrino, Elena Ceccotti, Chiara Pasquino, Samuela De Rosa, Cristina Grange, Stefania Tritta, Giovanni Camussi

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

13 citing papers in PubMed, 18 citations in OpenAlex.

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  10. State of the Art and New Trends from the 2022 Gism Annual Meeting.International journal of molecular sciences · 2023
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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 at 1 institution in 1 country.

Stefania BrunoDepartment of Medical Sciences, University of Torino, 10126 Torino, Italy.ORCID 0000-0002-8879-9536
Giulia ChiabottoDepartment of Medical Sciences, University of Torino, 10126 Torino, Italy.ORCID 0000-0002-1420-3517
Massimo CedrinoMolecular Biotechnology Center, University of Torino, 10126 Torino, Italy.
Elena CeccottiDepartment of Medical Sciences, University of Torino, 10126 Torino, Italy.ORCID 0000-0003-2704-5738
Chiara PasquinoDepartment of Medical Sciences, University of Torino, 10126 Torino, Italy.
Samuela De RosaDepartment of Medical Sciences, University of Torino, 10126 Torino, Italy.
Cristina GrangeDepartment of Medical Sciences, University of Torino, 10126 Torino, Italy.ORCID 0000-0002-6960-5476
Stefania TrittaMolecular Biotechnology Center, University of Torino, 10126 Torino, Italy.
Giovanni CamussiDepartment of Medical Sciences, University of Torino, 10126 Torino, Italy.ORCID 0000-0003-2795-232X
University of Turin · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The potential therapeutic effect of extracellular vesicles (EVs) that are derived from human liver stem cells (HLSCs) has been tested in an in vivo model of renal ischemia and reperfusion injury (IRI), that induce the development of chronic kidney disease (CKD). EVs were administered intravenously immediately after the IRI and three days later, then their effect was tested at different time points to evaluate how EV-treatment might interfere with fibrosis development. In IRI-mice that were sacrificed two months after the injury, EV- treatment decreased the development of interstitial fibrosis at the histological and molecular levels. Furthermore, the expression levels of pro-inflammatory genes and of epithelial-mesenchymal transition (EMT) genes were significantly reverted by EV-treatment. In IRI-mice that were sacrificed at early time points (two and three days after the injury), functional and histological analyses showed that EV-treatment induced an amelioration of the acute kidney injury (AKI) that was induced by IRI. Interestingly, at the molecular level, a reduction of pro-fibrotic and EMT-genes in sacrificed IRI-mice was observed at days two and three after the injury. These data indicate that in renal IRI, treatment with HLSC-derived EVs improves AKI and interferes with the development of subsequent CKD by modulating the genes that are involved in fibrosis and EMT.

Indexed as

Extracellular VesiclesLiverRenal Insufficiency, ChronicReperfusion InjuryStem CellsAnimalsHumansMaleMiceMice, Inbred BALB Cacute kidney injurychronic kidney diseaseepithelial-to-mesenchymal transitionrenal fibrosis

Identifiers

PMID35163409
PMCPMC8835844
OpenAlexW4210265311

What OpenQuestion holds

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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.