Evidence map›Paper›PMID 26349659›Full record

ArticleMucosal immunology2016

NLRP12 modulates host defense through IL-17A-CXCL1 axis.

S Cai, S Batra, F Del Piero, S Jeyaseelan

Open access · bronzeAbstract read
In one paragraph

Article in Mucosal immunology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

30 citing papers in PubMed, 47 citations in OpenAlex.

  1. Review
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  9. RMD open · 2023
    Review
  10. Article
  11. Review
  12. Article
  13. Host defense against the infection ofFrontiers in cellular and infection microbiology · 2022
    Review
  14. Host Defense againstJournal of immunology (Baltimore, Md. : 1950) · 2021
    Article
  15. Article
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  20. Observational
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

4 authors at 1 institution in 1 country.

S CaiLaboratory of Lung Biology, Department of Pathobiological Sciences and Center for Experimental Infectious Disease Research, Louisiana State University (LSU) School of Veterinary Medicine, Baton Rouge, Louisiana, USA.
S BatraLaboratory of Lung Biology, Department of Pathobiological Sciences and Center for Experimental Infectious Disease Research, Louisiana State University (LSU) School of Veterinary Medicine, Baton Rouge, Louisiana, USA.
F Del PieroLaboratory of Lung Biology, Department of Pathobiological Sciences and Center for Experimental Infectious Disease Research, Louisiana State University (LSU) School of Veterinary Medicine, Baton Rouge, Louisiana, USA.
S JeyaseelanLaboratory of Lung Biology, Department of Pathobiological Sciences and Center for Experimental Infectious Disease Research, Louisiana State University (LSU) School of Veterinary Medicine, Baton Rouge, Louisiana, USA.
Louisiana State University · US

Funding

TNF AND MCP-1 IN RETROVIRUS-INDUCED BRAIN DISEASEP20RR020159 · NCRR · LOUISIANA STATE UNIV A&M COL BATON ROUGE · PI KOUSOULAS, KONSTANTIN G · 2004 to 2011
$16.1M
Neutrophil Accumulation in Bacterial PneumoniaR01HL091958 · NHLBI · LOUISIANA STATE UNIV A&M COL BATON ROUGE · PI JEYASEELAN, SAMITHAMBY · 2008 to 2017
$3.8M
Neutrophil Function in Bacterial PneumoniaR01AI113720 · NIAID · LOUISIANA STATE UNIV A&M COL BATON ROUGE · PI JEYASEELAN, SAMITHAMBY · 2015 to 2019
$1.9M
NOD-Like Receptor Signaling is Critical to Secondhand Smoke-Induced Immunity andR15ES023151 · NIEHS · SOUTHERN UNIV A&M COL BATON ROUGE · PI BATRA, SANJAY · 2013 to 2016
$369k
NCRR NIH HHS P20 RR020159NHLBI NIH HHS R01 HL-091958NHLBI NIH HHS R01 HL091958NIAID NIH HHS R01 AI-113720NIAID NIH HHS R01 AI113720NIEHS NIH HHS R15-1R15ES023151-01NIEHS NIH HHS R15 ES023151
6 · The paper itself

Abstract

We used an extracellular pathogen Klebsiella pneumoniae to determine the role of NLRP12 (NOD-like receptor (NLR) family pyrin domain containing 12) as this bacterium is associated with devastating pulmonary infections. We found that human myeloid cells (neutrophils and macrophages) and non-myeloid cells (epithelial cells) show upregulation of NLRP12 in human pneumonic lungs. NLRP12-silenced human macrophages and murine Nlrp12(-/-) macrophages displayed reduced activation of nuclear factor-κB and mitogen-activated protein kinase, as well as expression of histone deacetylases following K. pneumoniae infection. NLRP12 is important for the production of interleukin-1β (IL-1β) in human and murine macrophages following K. pneumoniae infection. Furthermore, host survival, bacterial clearance, and neutrophil recruitment are dependent on NLRP12 following K. pneumoniae infection. Using bone marrow chimeras, we showed that hematopoietic cell-driven NLRP12 signaling predominantly contributes to host defense against K. pneumoniae. Intratracheal administration of either IL-17A+ CD4 T cells or chemokine (C-X-C motif) ligand 1 (CXCL1+) macrophages rescues host survival, bacterial clearance, and neutrophil recruitment in Nlrp12(-/-) mice following K. pneumoniae infection. These novel findings reveal the critical role of NLRP12-IL-17A-CXCL1 axis in host defense by modulating neutrophil recruitment against this extracellular pathogen.

Indexed as

AnimalsBone MarrowCD4-Positive T-LymphocytesChemokine CXCL1Epithelial CellsFemaleGene Expression RegulationHumansInterleukin-17Intracellular Signaling Peptides and ProteinsKlebsiella InfectionsKlebsiella pneumoniaeLungMacrophagesMiceMice, Inbred C57BLChemokine CXCL1Cxcl1 protein, mouseInterleukin-17Intracellular Signaling Peptides and ProteinsNLRP12 protein, mouse

Identifiers

PMID26349659
PMCPMC5089371
OpenAlexW1466085076

What OpenQuestion holds

Textmetadata
LicenceTDM
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.