Evidence map›Paper›PMID 33547278›Full record

ArticleCell death & disease2021

Sensing soluble uric acid by Naip1-Nlrp3 platform.

Tarcio Teodoro Braga, Mariana Rodrigues Davanso, Davi Mendes, Tiago Antonio de Souza, Anderson Fernandes de Brito, Mario Costa Cruz, Meire Ioshie Hiyane, Dhemerson Souza de Lima, Vinicius Nunes, Juliana de Fátima Giarola and 9 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

18 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Article
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  6. Macrophage variants in laboratory research: most are well done, but some are RAW.Frontiers in cellular and infection microbiology · 2024
    Review
  7. Canonical and non-canonical functions of NLRP3.Journal of advanced research · 2023
    Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Uric Acid in Inflammation and the Pathogenesis of Atherosclerosis.International journal of molecular sciences · 2021
    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

19 authors at 6 institutions in 5 countries.

Tarcio Teodoro BragaDepartment of Basic Pathology, Federal University of Parana, Curitiba, PR, Brazil. tarcio.braga@ufpr.br.ORCID http://orcid.org/0000-0002-2989-1076
Mariana Rodrigues DavansoDepartment of Immunology, Institute of Biomedical Sciences IV, University of São Paulo, São Paulo, SP, Brazil.
Davi MendesDepartment of Microbiology, Institute of Biomedical Sciences II, University of São Paulo, São Paulo, SP, Brazil.ORCID http://orcid.org/0000-0002-9524-4424
Tiago Antonio de SouzaDepartment of Microbiology, Institute of Biomedical Sciences II, University of São Paulo, São Paulo, SP, Brazil.
Anderson Fernandes de BritoDepartment of Life Sciences, Imperial College London, London, SW7 2AZ, UK.
Mario Costa CruzDepartment of Immunology, Institute of Biomedical Sciences IV, University of São Paulo, São Paulo, SP, Brazil.
Meire Ioshie HiyaneDepartment of Immunology, Institute of Biomedical Sciences IV, University of São Paulo, São Paulo, SP, Brazil.
Dhemerson Souza de LimaDepartment of Immunology, Institute of Biomedical Sciences IV, University of São Paulo, São Paulo, SP, Brazil.
Vinicius NunesDepartment of Immunology, Institute of Biomedical Sciences IV, University of São Paulo, São Paulo, SP, Brazil.
Juliana de Fátima GiarolaInstitute of Chemistry, University of Campinas, Campinas, SP, Brazil.
Denio Emanuel Pires SoutoInstitute of Chemistry, University of Campinas, Campinas, SP, Brazil.
Tomasz PróchnickiInstitute of Innate Immunity, University Hospitals Bonn, Bonn, Germany.
Mario LauterbachInstitute of Innate Immunity, University Hospitals Bonn, Bonn, Germany.
Stellee Marcela Petris BiscaiaDepartment of Cellular Biology, Federal University of Parana, Curitiba, PR, Brazil.
Rilton Alves de FreitasDepartment of Chemistry, Federal University of Parana, Curitiba, PR, Brazil.
Rui CuriDepartment of Physiology and Biophysics, Institute of Biomedical Sciences I, University of Sao Paulo, São Paulo, SP, Brazil.
Alessandra PontilloDepartment of Immunology, Institute of Biomedical Sciences IV, University of São Paulo, São Paulo, SP, Brazil.
Eicke Latz *Institute of Innate Immunity, University Hospitals Bonn, Bonn, Germany.ORCID http://orcid.org/0000-0003-1488-5666
Niels Olsen Saraiva Camara *Department of Immunology, Institute of Biomedical Sciences IV, University of São Paulo, São Paulo, SP, Brazil.
Universidade de São Paulo · BRUniversidade Estadual de Campinas (UNICAMP) · BRUniversidade Federal do Paraná · BRUniversity Hospital Bonn · DEImperial College London · GBUniversity of Massachusetts Chan Medical School · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Uric acid (UA), a product of purine nucleotide degradation able to initiate an immune response, represents a breakpoint in the evolutionary history of humans, when uricase, the enzyme required for UA cleavage, was lost. Despite being inert in human cells, UA in its soluble form (sUA) can increase the level of interleukin-1β (IL-1β) in murine macrophages. We, therefore, hypothesized that the recognition of sUA is achieved by the Naip1-Nlrp3 inflammasome platform. Through structural modelling predictions and transcriptome and functional analyses, we found that murine Naip1 expression in human macrophages induces IL-1β expression, fatty acid production and an inflammation-related response upon sUA stimulation, a process reversed by the pharmacological and genetic inhibition of Nlrp3. Moreover, molecular interaction experiments showed that Naip1 directly recognizes sUA. Accordingly, Naip may be the sUA receptor lost through the human evolutionary process, and a better understanding of its recognition may lead to novel anti-hyperuricaemia therapies.

Indexed as

AnimalsFatty AcidsHumansInflammasomesInterleukin-1betaMacaca mulattaMacrophagesMiceMice, Inbred C57BLNeuronal Apoptosis-Inhibitory ProteinNLR Family, Pyrin Domain-Containing 3 ProteinProtein BindingTHP-1 CellsUric AcidFatty AcidsIL1B protein, humanInflammasomesInterleukin-1betaNaip1 protein, mouseNAIP protein, humanNeuronal Apoptosis-Inhibitory ProteinNLR Family, Pyrin Domain-Containing 3 ProteinNLRP3 protein, humanNlrp3 protein, mouseUric Acid

Identifiers

PMID33547278
PMCPMC7864962
OpenAlexW3126269755

What OpenQuestion holds

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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.