Evidence map›Paper›PMID 25609235›Full record

ArticleNature communications2015

Autophagy enhances NFκB activity in specific tissue macrophages by sequestering A20 to boost antifungal immunity.

Masashi Kanayama, Makoto Inoue, Keiko Danzaki, Gianna Hammer, You-Wen He, Mari L Shinohara

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 76 papers.

0numbers the graph read from it
0cells of the map it votes in
76citing papers in PubMed
8.7field-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

76 citing papers in PubMed, 110 citations in OpenAlex.

  1. Review
  2. Article
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  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Modern Technologies in Diagnosis of Fungal Keratitis (Review).Sovremennye tekhnologii v meditsine · 2023
    Review
  13. Review
  14. Article
  15. Review
  16. Review
  17. A dynamically evolving war between autophagy and pathogenic microorganisms.Journal of Zhejiang University. Science. B · 2022
    Article
  18. Autophagy and Skin Diseases.Frontiers in pharmacology · 2022
    Review
  19. Article
  20. Review

16 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

6 authors at 2 institutions in 1 country.

Masashi KanayamaDepartment of Immunology, Duke University Medical Center, Durham, North Carolina 27710, USA.
Makoto InoueDepartment of Immunology, Duke University Medical Center, Durham, North Carolina 27710, USA.
Keiko DanzakiDepartment of Immunology, Duke University Medical Center, Durham, North Carolina 27710, USA.
Gianna HammerDepartment of Immunology, Duke University Medical Center, Durham, North Carolina 27710, USA.
You-Wen HeDepartment of Immunology, Duke University Medical Center, Durham, North Carolina 27710, USA.
Mari L Shinohara1] Department of Immunology, Duke University Medical Center, Durham, North Carolina 27710, USA [2] Department of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, North Carolina 27710, USA.
Duke Medical Center · USDuke University Hospital · US

Funding

Role of osteopontin in innate immunity during infections and inflammationR01AI088100 · NIAID · DUKE UNIVERSITY · PI SHINOHARA, MARI L. · 2011 to 2021
$4.3M
Regulation of innate inflammation by CD40 signaling and intracellular osteopontinR21AI103584 · NIAID · DUKE UNIVERSITY · PI SHINOHARA, MARI L. · 2014 to 2015
$432k
NIAID NIH HHS R01 AI088100NIAID NIH HHS R01AI088100NIAID NIH HHS R21 AI103584
6 · The paper itself

Abstract

Immune responses must be well restrained in a steady state to avoid excessive inflammation. However, such restraints are quickly removed to exert antimicrobial responses. Here we report a role of autophagy in an early host antifungal response by enhancing NFκB activity through A20 sequestration. Enhancement of NFκB activation is achieved by autophagic depletion of A20, an NFκB inhibitor, in F4/80(hi) macrophages in the spleen, peritoneum and kidney. We show that p62, an autophagic adaptor protein, captures A20 to sequester it in the autophagosome. This allows the macrophages to release chemokines to recruit neutrophils. Indeed, mice lacking autophagy in myeloid cells show higher susceptibility to Candida albicans infection due to impairment in neutrophil recruitment. Thus, at least in the specific aforementioned tissues, autophagy appears to break A20-dependent suppression in F4/80(hi) macrophages, which express abundant A20 and contribute to the initiation of efficient innate immune responses.

Indexed as

AutophagyAnimalsAutophagy-Related Protein 7Candida albicansCandidiasisChemokine CXCL1Chemokine CXCL2ChemokinesChemotaxisCysteine EndopeptidasesDown-RegulationFemaleImmunity, InnateInflammationIntracellular Signaling Peptides and ProteinsKidneyAtg7 protein, mouseAutophagy-Related Protein 7Chemokine CXCL1Chemokine CXCL2ChemokinesCxcl1 protein, mouseCxcl2 protein, mouseCysteine EndopeptidasesIntracellular Signaling Peptides and ProteinsMicrotubule-Associated ProteinsNF-kappa B p50 SubunitNfkb1 protein, mouseTnfaip3 protein, mouseTumor Necrosis Factor alpha-Induced Protein 3

Identifiers

PMID25609235
PMCPMC4304414
OpenAlexW1984813184

What OpenQuestion holds

Textmetadata
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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.