Evidence map›Paper›PMID 24398679›Full record

ArticleThe Journal of biological chemistry2014

Localization and functionality of the inflammasome in neutrophils.

Martina Bakele, Melanie Joos, Sofia Burdi, Nicolas Allgaier, Simone Pöschel, Birgit Fehrenbacher, Martin Schaller, Veronica Marcos, Jasmin Kümmerle-Deschner, Nikolaus Rieber and 4 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 90 papers.

0numbers the graph read from it
0cells of the map it votes in
90citing papers in PubMed
6.5field-weighted citation impact, top 2% 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

90 citing papers in PubMed, 153 citations in OpenAlex.

  1. Trial
  2. Review
  3. IL-1 family cytokines in inflammation and immunity.Cellular & molecular immunology · 2025
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  7. Article
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  14. Role of NLRP3 inflammasome-mediated neuronal pyroptosis and neuroinflammation in neurodegenerative diseases.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2023
    Review
  15. Review
  16. Review
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  18. Article
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30 more citing papers are in PubMed but not listed here.

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 4 institutions in 3 countries.

Martina BakeleFrom the Departments of Pediatrics I and.
Melanie Joos
Sofia Burdi
Nicolas Allgaier
Simone Pöschel
Birgit Fehrenbacher
Martin Schaller
Veronica Marcos
Jasmin Kümmerle-Deschner
Nikolaus Rieber
Niels Borregaard
Amir Yazdi
Andreas Hector
Dominik Hartl
University of Tübingen · DECopenhagen University Hospital · DKLudwig-Maximilians-Universität München · DEPediatrics and Genetics · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neutrophils represent the major fraction of circulating immune cells and are rapidly recruited to sites of infection and inflammation. The inflammasome is a multiprotein complex that regulates the generation of IL-1 family proteins. The precise subcellular localization and functionality of the inflammasome in human neutrophils are poorly defined. Here we demonstrate that highly purified human neutrophils express key components of the NOD-like receptor family, pyrin domain containing 3 (NLRP3), and absent in melanoma 2 (AIM2) inflammasomes, particularly apoptosis-associated speck-like protein containing a CARD (ASC), AIM2, and caspase-1. Subcellular fractionation and microscopic analyses further showed that inflammasome components were localized in the cytoplasm and also noncanonically in secretory vesicle and tertiary granule compartments. Whereas IL-1β and IL-18 were expressed at the mRNA level and released as protein, highly purified neutrophils neither expressed nor released IL-1α at baseline or upon stimulation. Upon inflammasome activation, highly purified neutrophils released substantially lower levels of IL-1β protein compared with partially purified neutrophils. Serine proteases and caspases were differentially involved in IL-1β release, depending on the stimulus. Spontaneous activation of the NLRP3 inflammasome in neutrophils in vivo affected IL-1β, but not IL-18 release. In summary, these studies show that human neutrophils express key components of the inflammasome machinery in distinct intracellular compartments and release IL-1β and IL-18, but not IL-1α or IL-33 protein. Targeting the neutrophil inflammasome may represent a future therapeutic strategy to modulate neutrophilic inflammatory diseases, such as cystic fibrosis, rheumatoid arthritis, or sepsis.

Indexed as

AdultCarrier ProteinsCaspasesCell CompartmentationGene Expression ProfilingHumansInflammasomesInterleukinsIntracellular SpaceNeutrophilsNLR Family, Pyrin Domain-Containing 3 ProteinProtein TransportRNA, MessengerSerine ProteasesSubcellular FractionsCarrier ProteinsCaspasesInflammasomesInterleukinsNLR Family, Pyrin Domain-Containing 3 ProteinNLRP3 protein, humanRNA, MessengerSerine ProteasesCytokineImmunityInflammationInnate ImmunityNeutrophilsPathogen-associated Molecular Pattern (PAMP)Toll-like Receptor (TLR)

Identifiers

PMID24398679
PMCPMC3931087
OpenAlexW1989853799

What OpenQuestion holds

Textmetadata
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.