Evidence map›Paper›PMID 35204131›Full record

ReviewAntioxidants (Basel, Switzerland)2022

Involvement of Inflammasome Components in Kidney Disease.

Ana Karina Aranda-Rivera, Anjali Srivastava, Alfredo Cruz-Gregorio, José Pedraza-Chaverri, Shrikant R Mulay, Alexandra Scholze

Open access · goldAbstract readReview
In one paragraph

Review in Antioxidants (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
4.8field-weighted citation impact, top 4% 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

23 citing papers in PubMed, 58 citations in OpenAlex.

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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

6 authors at 3 institutions in 3 countries.

Ana Karina Aranda-RiveraLaboratory F-315, Department of Biology, Faculty of Chemistry, National Autonomous University of Mexico, Mexico City 04510, Mexico.ORCID 0000-0002-4095-754X
Anjali SrivastavaDivision of Pharmacology, CSIR-Central Drug Research Institute, Lucknow 226031, India.
Alfredo Cruz-GregorioLaboratory F-315, Department of Biology, Faculty of Chemistry, National Autonomous University of Mexico, Mexico City 04510, Mexico.ORCID 0000-0003-0077-5079
José Pedraza-ChaverriLaboratory F-315, Department of Biology, Faculty of Chemistry, National Autonomous University of Mexico, Mexico City 04510, Mexico.ORCID 0000-0001-6628-4411
Shrikant R MulayDivision of Pharmacology, CSIR-Central Drug Research Institute, Lucknow 226031, India.ORCID 0000-0003-4261-445X
Alexandra ScholzeDepartment of Nephrology, Odense University Hospital, Odense, Denmark, and Institute of Clinical Research, University of Southern Denmark, 5000 Odense C, Denmark.ORCID 0000-0002-3100-8692
Universidad Nacional Autónoma de México · MXCentral Drug Research Institute · INUniversity of Southern Denmark · DK

Funding

Consejo Nacional de Ciencia y Tecnología A1-S-7495Dirección General de Asuntos del Personal Académico IN200922
6 · The paper itself

Abstract

Inflammasomes are multiprotein complexes with an important role in the innate immune response. Canonical activation of inflammasomes results in caspase-1 activation and maturation of cytokines interleukin-1β and -18. These cytokines can elicit their effects through receptor activation, both locally within a certain tissue and systemically. Animal models of kidney diseases have shown inflammasome involvement in inflammation, pyroptosis and fibrosis. In particular, the inflammasome component nucleotide-binding domain-like receptor family pyrin domain containing 3 (NLRP3) and related canonical mechanisms have been investigated. However, it has become increasingly clear that other inflammasome components are also of importance in kidney disease. Moreover, it is becoming obvious that the range of molecular interaction partners of inflammasome components in kidney diseases is wide. This review provides insights into these current areas of research, with special emphasis on the interaction of inflammasome components and redox signalling, endoplasmic reticulum stress, and mitochondrial function. We present our findings separately for acute kidney injury and chronic kidney disease. As we strictly divided the results into preclinical and clinical data, this review enables comparison of results from those complementary research specialities. However, it also reveals that knowledge gaps exist, especially in clinical acute kidney injury inflammasome research. Furthermore, patient comorbidities and treatments seem important drivers of inflammasome component alterations in human kidney disease.

Indexed as

acute kidney injuryAIM2caspase-8chronic kidney diseaseendoplasmic reticulum stressinflammasomeinterleukin-18interleukin-1βkidney transplantationNLRP3redox signalling

Identifiers

PMID35204131
PMCPMC8868482
OpenAlexW4210453189

What OpenQuestion holds

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LicenceCC BY
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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.