Evidence map›Paper›PMID 16186496›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2005

Human airway epithelial cell determinants of survival and functional phenotype for primary human mast cells.

F H Hsieh, P Sharma, A Gibbons, T Goggans, S C Erzurum, S J Haque

Open access · greenAbstract readComparative Study
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
0.6field-weighted citation impact, top 33% 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

19 citing papers in PubMed, 56 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Observational
  8. Article
  9. Article
  10. Article
  11. Mast cells in airway diseases and interstitial lung disease.European journal of pharmacology · 2016
    Review
  12. Article
  13. Activity of the leukotriene pathway in Barrett's metaplasia and oesophageal adenocarcinoma.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2012
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. 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

6 authors at 1 institution in 1 country.

F H HsiehDepartment of Pulmonary, Allergy, and Critical Care Medicine, Cleveland Clinic Foundation, 9500 Euclid Avenue, Cleveland, OH 44195, USA. hsiehf@ccf.org
P Sharma
A Gibbons
T Goggans
S C Erzurum
S J Haque
Cleveland Clinic · US

Funding

VIRALLY-INDUCED STAT-1, STAT-3 AND STAT-6M01RR018390 · NCRR · CLEVELAND CLINIC LERNER COM-CWRU · PI SCHREIBER, MARTIN A · 2003 to 2007
$11.0M
NEGATIVE REGULATION OF INTERLEUKIN-4 SIGNALINGR01GM060533 · NIGMS · CLEVELAND CLINIC LERNER COL/MED-CWRU · PI HAQUE, SAIKH JAHARUL · 2000 to 2004
$957k
Effector mechanisms in allergic inflammationK08HL074129 · NHLBI · CLEVELAND CLINIC LERNER COM-CWRU · PI HSIEH, FRED H · 2003 to 2007
$633k
NO SYNTHESIS AND CONSUMPTION IN THE LUNGK24HL004265 · NHLBI · CLEVELAND CLINIC LERNER COL/MED-CWRU · PI ERZURUM, SERPIL C. · 2000 to 2004
$510k
NCRR NIH HHS M01 RR018390NCRR NIH HHS RR018390NHLBI NIH HHS HL04265NHLBI NIH HHS HL074129NHLBI NIH HHS K08 HL074129NHLBI NIH HHS K24 HL004265NIAID NIH HHS AI70649NIGMS NIH HHS GM060533NIGMS NIH HHS R01 GM060533
6 · The paper itself

Abstract

Mast cells (MCs) are found in increased numbers at airway mucosal surfaces in asthmatic patients. Because human airway epithelial cells (HAECs) actively participate in airway inflammatory responses and are in direct contact with MCs in the mucosa, we hypothesized that HAEC-MC interactions may contribute to the differentiation and survival of MCs in the airway mucosa. Here, we show that HAECs express mRNA and protein for soluble and membrane-bound stem cell factor, releasing soluble stem cell factor into the cell culture supernatant at a concentration of 5.9 +/- 0.1 ng per 10(6) HAEC. HAECs were able to support MC survival in coculture in the absence of any exogenous cytokines for at least 4 d. Before the initiation of coculture, MCs were uniformly tryptase and chymase (MC(TC)) double positive, but by 2 d of coculture the majority of MCs expressed tryptase (MC(T)) alone. MCs supported in coculture generated low amounts of cysteinyl-leukotrienes (cys-LT) after FcepsilonRI-dependent activation (0.2 +/- 0.1 ng of cys-LT per 10(6) cells) and required priming with IL-4 and IL-3 during coculture to achieve a quantity of cys-LT generation within the range expected for human lung mucosal MC (26.5 +/- 16 ng of cys-LT per 10(6) cells). In these culture conditions, HAECs were able to direct mucosal MC protease phenotype, but T cell-derived Th2 cytokines were required for the expression of a functional airway MC eicosanoid phenotype. Thus, distinct cell types may direct unique aspects of reactive mucosal MC phenotype in the airways.

Indexed as

PhenotypeAnalysis of VarianceCell Culture TechniquesCell DifferentiationCell SurvivalChymasesCysteineCytokinesDNA PrimersEnzyme-Linked Immunosorbent AssayHumansImmunohistochemistryLeukotrienesMast CellsRespiratory MucosaReverse Transcriptase Polymerase Chain ReactionChymasesCysteinecysteinyl-leukotrieneCytokinesDNA PrimersLeukotrienesSerine EndopeptidasesStem Cell FactorTryptases

Identifiers

PMID16186496
PMCPMC1242292
OpenAlexW2060449890

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.