Evidence map›Paper›PMID 22627362›Full record

ArticleInternational archives of allergy and immunology2012

Alternaria fungus induces the production of GM-CSF, interleukin-6 and interleukin-8 and calcium signaling in human airway epithelium through protease-activated receptor 2.

Yoshinori Matsuwaki, Kota Wada, Thomas White, Hiroshi Moriyama, Hirohito Kita

Open access · bronzeAbstract read
In one paragraph

Article in International archives of allergy and immunology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

44 citing papers in PubMed, 84 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. ATP functions as a primary alarmin in allergen-induced type 2 immunity.American journal of physiology. Cell physiology · 2023
    Review
  6. Article
  7. Allergen-induced DNA release by the airway epithelium amplifies type 2 immunity.The Journal of allergy and clinical immunology · 2023
    Article
  8. Immunopathologic Role of Fungi in Chronic Rhinosinusitis.International journal of molecular sciences · 2023
    Review
  9. Article
  10. Article
  11. Frontiers in immunology · 2022
    Article
  12. Article
  13. Article
  14. Journal of fungi (Basel, Switzerland) · 2021
    Review
  15. PAR-2-activated secretion by airway gland serous cells: role for CFTR and inhibition byAmerican journal of physiology. Lung cellular and molecular physiology · 2021
    Article
  16. Article
  17. The Airway Epithelium-A Central Player in Asthma Pathogenesis.International journal of molecular sciences · 2020
    Review
  18. Article
  19. Article
  20. Article
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

5 authors at 3 institutions in 2 countries.

Yoshinori MatsuwakiDepartment of Immunology and Medicine, Mayo Clinic, Rochester, Minn, USA. matuwaki@jikei.ac.jp
Kota Wada
Thomas White
Hiroshi Moriyama
Hirohito Kita
Mayo Clinic · USJikei University School of Medicine · JPMayo Clinic in Arizona · US

Funding

The Pathogenesis of Chronic RhinosinusitisR01AI049235 · NIAID · MAYO CLINIC ROCHESTER · PI KITA, HIROHITO · 2001 to 2011
$4.5M
MECHANISMS OF EOSINOPHIL DEGRANULATION IN HUMAN DISEASER01AI034486 · NIAID · MAYO CLINIC ROCHESTER · PI KITA, HIROHITO · 2000 to 2010
$3.2M
Mechanisms of Eosinophilic Inflammation in Human DiseaseR56AI034486 · NIAID · MAYO CLINIC ROCHESTER · PI KITA, HIROHITO · 2005 to 2012
$769k
The Pathogenesis of Chronic RhinosinusitisR56AI049235 · NIAID · MAYO CLINIC ROCHESTER · PI KITA, HIROHITO · 2012 to 2012
$278k
MECHANISMS OF EOSINOPHIL DEGRANULATIONR29AI034486 · NIAID · MAYO CLINIC COLL OF MEDICINE, ROCHESTER · PI KITA, HIROHITO · 1994 to 1998
–
NIAID NIH HHS AI34486NIAID NIH HHS AI49235NIAID NIH HHS R01 AI034486NIAID NIH HHS R01 AI049235NIAID NIH HHS R29 AI034486NIAID NIH HHS R56 AI034486NIAID NIH HHS R56 AI049235
6 · The paper itself

Abstract

rationaleRecent studies suggest that host immune responses to environmental fungi may play an important role in the development of allergic diseases, such as human asthma. Epithelium is considered an active participant in allergic inflammation. We previously reported that aspartate protease from Alternaria induces the activation and degranulation of human eosinophils that are mediated through protease-activated receptor 2 (PAR-2). However, our current knowledge on the innate immune responses of epithelium to environmental fungi is very limited. We investigated the responses of epithelium to fungi and the mechanisms of these responses.

methodsHuman airway epithelial cell line BEAS-2B and Calu-3 (both from American Type Culture Collection) were incubated with PAR-2 peptides and extracts of various fungi. The cellular responses, including GM-CSF, interleukin (IL)-6, IL-8, eotaxin, eotaxin-2 and RANTES production as well as increases in intracellular calcium concentration ([Ca(2+)](i)), were examined. To characterize the proteases involved in these responses, protease inhibitors such as pepstatin A and alkalo-thermophilic Bacillus inhibitor (ATBI), HIV protease inhibitors and 4-amidinophenylmethanesulfonyl fluoride hydrochloride were used. To investigate the role of PAR-2, PAR-2-agonistic and PAR-2-antagonistic peptides were used.

resultsPAR-2-activating peptide, but not the control peptide, induced GM-CSF, IL-6 and IL-8 production; these cellular responses were accompanied by a quick and marked increase in [Ca(2+)](i). Among 7 common environmental fungi, only Alternaria induced GM-CSF, IL-6 and IL-8 production and increased [Ca(2+)](i) response. Both cytokine production and increased [Ca(2+)](i) were significantly inhibited by PAR-2 antagonist peptide and by aspartate protease inhibitors (pepstatin A, ritonavir, nelfinavir and ATBI), but not by the PAR-2 control peptide or by other protease inhibitors.

conclusionsAspartate proteases from Alternaria induce cytokine production and calcium response in airway epithelium that is mediated through PAR-2. This protease-mediated activation of airway epithelium may be implicated in the development and exacerbation of airway allergic disease.

Indexed as

AlternariaCalcium SignalingCell LineCytokinesEosinophilsEpithelial CellsEpitheliumHumansOligopeptidesProtease InhibitorsReceptor, PAR-2Respiratory SystemCytokinesOligopeptidesProtease InhibitorsReceptor, PAR-2

Identifiers

PMID22627362
PMCPMC3395436
OpenAlexW2136378686

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.