Evidence map›Paper›PMID 26451347›Full record

ArticleTissue barriers

Low molecular weight components of pollen alter bronchial epithelial barrier functions.

Cornelia Blume, Emily J Swindle, Stefanie Gilles, Claudia Traidl-Hoffmann, Donna E Davies

Open access · bronzeAbstract read
In one paragraph

Article in Tissue barriers. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.2field-weighted citation impact, top 24% 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

17 citing papers in PubMed, 32 citations in OpenAlex.

  1. Review
  2. Article
  3. Special Issue "Molecular and Cellular Advances in Atopic Diseases".International journal of molecular sciences · 2024
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. 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 4 institutions in 2 countries.

Cornelia BlumeBrooke Laboratory; Clinical and Experimental Sciences; Faculty of Medicine; University of Southampton; University Hospital Southampton ; Southampton, UK.
Emily J SwindleBrooke Laboratory; Clinical and Experimental Sciences; Faculty of Medicine; University of Southampton; University Hospital Southampton ; Southampton, UK.
Stefanie GillesInstitute of Environmental Medicine; UNIKA-T; Technische Universität Munich ; Munich, Germany ; CK CARE; Christine Kühne Center for Allergy Research and Education ; Davos, Switzerland.
Claudia Traidl-HoffmannInstitute of Environmental Medicine; UNIKA-T; Technische Universität Munich ; Munich, Germany ; CK CARE; Christine Kühne Center for Allergy Research and Education ; Davos, Switzerland.
Donna E DaviesBrooke Laboratory; Clinical and Experimental Sciences; Faculty of Medicine; University of Southampton; University Hospital Southampton ; Southampton, UK ; Southampton NIHR Respiratory Biomedical Research Unit; University Hospital Southampton ; Southampton, UK.
CK-CARE · CHFaculty (United Kingdom) · GBUniversity Hospital Southampton NHS Foundation Trust · GBUniversity of Southampton · GB

Funding

Medical Research Council G0900453
6 · The paper itself

Abstract

The bronchial epithelium plays a key role in providing a protective barrier against many environmental substances of anthropogenic or natural origin which enter the lungs during breathing. Appropriate responses to these agents are critical for regulation of tissue homeostasis, while inappropriate responses may contribute to disease pathogenesis. Here, we compared epithelial barrier responses to different pollen species, characterized the active pollen components and the signaling pathways leading to epithelial activation. Polarized bronchial cells were exposed to extracts of timothy grass (Phleum pratense), ragweed (Ambrosia artemisifolia), mugwort (Artemisia vulgaris), birch (Betula alba) and pine (Pinus sylvestris) pollens. All pollen species caused a decrease in ionic permeability as monitored trans-epithelial electrical resistance (TER) and induced polarized release of mediators analyzed by ELISA, with grass pollen showing the highest activity. Ultrafiltration showed that the responses were due to components <3kDa. However, lipid mediators, including phytoprostane E1, had no effect on TER, and caused only modest induction of mediator release. Reverse-phase chromatography separated 2 active fractions: the most hydrophilic maximally affected cytokine release whereas the other only affected TER. Inhibitor studies revealed that JNK played a more dominant role in regulation of barrier permeability in response to grass pollen exposure, whereas ERK and p38 controlled cytokine release. Adenosine and the flavonoid isorhamnetin present in grass pollen contributed to the overall effect on airway epithelial barrier responses. In conclusion, bronchial epithelial barrier functions are differentially affected by several low molecular weight components released by pollen. Furthermore, ionic permeability and innate cytokine production are differentially regulated.

Indexed as

bronchial epithelial barrierpolarized mediator releasepollenpollen-associated lipid mediatortight junctions

Identifiers

PMID26451347
PMCPMC4574901
OpenAlexW1602708848

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.