Evidence map›Paper›PMID 27306366›Full record

ArticleAmerican journal of physiology. Cell physiology2016

Differentiation of human bronchial epithelial cells: role of hydrocortisone in development of ion transport pathways involved in mucociliary clearance.

Nathan A Zaidman, Angela Panoskaltsis-Mortari, Scott M O'Grady

Open access · bronzeAbstract read
In one paragraph

Article in American journal of physiology. Cell physiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.5field-weighted citation impact, top 16% 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

10 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Dexamethasone Creates a Suppressive Microenvironment and PromotesJournal of fungi (Basel, Switzerland) · 2021
    Article
  7. Oxygenation as a driving factor in epithelial differentiation at the air-liquid interface.Integrative biology : quantitative biosciences from nano to macro · 2021
    Article
  8. Article
  9. Characterizing well-differentiated culture of primary human nasal epithelial cells for use in wound healing assays.Laboratory investigation; a journal of technical methods and pathology · 2018
    Article
  10. Large-conductance CaThe Journal of physiology · 2017
    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

3 authors at 1 institution in 1 country.

Nathan A ZaidmanDepartment of Integrative Biology and Physiology, University of Minnesota, Minneapolis, Minnesota;
Angela Panoskaltsis-MortariDepartment of Integrative Biology and Physiology, University of Minnesota, Minneapolis, Minnesota; Department of Pediatrics, University of Minnesota, Minneapolis, Minnesota; and.
Scott M O'GradyDepartment of Integrative Biology and Physiology, University of Minnesota, Minneapolis, Minnesota; Department of Animal Science, University of Minnesota, Minneapolis, Minnesota ograd001@umn.edu.
University of Minnesota · US

Funding

Overcoming Barriers to Bioengineering 3-D Human LungR01HL108627 · NHLBI · UNIVERSITY OF MINNESOTA · PI PANOSKALTSIS-MORTARI, ANGELA, TAYLOR, DORIS A · 2011 to 2014
$3.0M
Allergen-induced IL-33 release by the airway epitheliumR01HL110539 · NHLBI · MAYO CLINIC ROCHESTER · PI KITA, HIROHITO, O'GRADY, SCOTT M. · 2011 to 2014
$2.0M
Engineering human iPS cells into an airway epithelium capable of ion transportF31EB018707 · NIBIB · UNIVERSITY OF MINNESOTA · PI ZAIDMAN, NATHAN A · 2014 to 2015
$58k
NHLBI NIH HHS R01 HL108627NHLBI NIH HHS R01 HL110539NIBIB NIH HHS F31 EB018707
6 · The paper itself

Abstract

Glucocorticoids strongly influence the mucosal-defense functions performed by the bronchial epithelium, and inhaled corticosteroids are critical in the treatment of patients with inflammatory airway diseases such as asthma, chronic obstructive pulmonary disease, and cystic fibrosis. A common pathology associated with these diseases is reduced mucociliary clearance, a defense mechanism involving the coordinated transport of salt, water, and mucus by the bronchial epithelium, ultimately leading to retention of pathogens and particles in the airways and to further disease progression. In the present study we investigated the role of hydrocortisone (HC) in differentiation and development of the ion transport phenotype of normal human bronchial epithelial cells under air-liquid interface conditions. Normal human bronchial epithelial cells differentiated in the absence of HC (HC0) showed significantly less benzamil-sensitive short-circuit current than controls, as well as a reduced response after stimulation with the selective β2-adrenergic receptor agonist salbutamol. Apical membrane localization of epithelial Na(+) channel α-subunits was similarly reduced in HC0 cells compared with controls, supporting a role of HC in the trafficking and density of Na(+) channels in the plasma membrane. Additionally, glucocorticoid exposure during differentiation regulated the transcription of cystic fibrosis transmembrane conductance regulator and β2-adrenergic receptor mRNAs and appeared to be necessary for the expression of cystic fibrosis transmembrane conductance regulator-dependent anion secretion in response to β2-agonists. HC had no significant effect on surface cell differentiation but did modulate the expression of mucin mRNAs. These findings indicate that glucocorticoids support mucosal defense by regulating critical transport pathways essential for effective mucociliary clearance.

Indexed as

AmilorideBronchiCell DifferentiationCells, CulturedCystic FibrosisCystic Fibrosis Transmembrane Conductance RegulatorEpithelial CellsEpithelial Sodium ChannelsHumansHydrocortisoneIon TransportMucinsMucociliary ClearanceReceptors, Adrenergic, beta-2Respiratory MucosaSodiumAmiloridebenzamilCystic Fibrosis Transmembrane Conductance RegulatorEpithelial Sodium ChannelsHydrocortisoneMucinsReceptors, Adrenergic, beta-2Sodiumcystic fibrosis transmembrane conductance regulatorepithelial ion transportepithelial sodium channelsalbutamolβ2-adrenergic receptors

Identifiers

PMID27306366
PMCPMC5129773
OpenAlexW2430636228

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.