Evidence map›Paper›PMID 30300884›Full record

ArticleCells, tissues, organs2018

Na+/H+ Exchangers Are Required for the Development and Function of Vertebrate Mucociliary Epithelia.

Dingyuan I Sun, Alexia Tasca, Maximilian Haas, Grober Baltazar, Richard M Harland, Walter E Finkbeiner, Peter Walentek

Open access · greenAbstract read
In one paragraph

Article in Cells, tissues, organs, 2018. 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 17% 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, 18 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Role of Genetic Mutations of the NaMolecular and cellular biochemistry · 2021
    Review
  7. Article
  8. Article
  9. Article
  10. 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

7 authors at 5 institutions in 4 countries.

Dingyuan I SunGenetics, Genomics and Development Division, Molecular and Cell Biology Department, University of California, Berkeley, California, USA.
Alexia TascaRenal Division, Department of Medicine, University Freiburg Medical Center and ZBSA - Center for Systems Biological Analysis, Freiburg, Germany.
Maximilian HaasRenal Division, Department of Medicine, University Freiburg Medical Center and ZBSA - Center for Systems Biological Analysis, Freiburg, Germany.
Grober BaltazarGenetics, Genomics and Development Division, Molecular and Cell Biology Department, University of California, Berkeley, California, USA.
Richard M HarlandGenetics, Genomics and Development Division, Molecular and Cell Biology Department, University of California, Berkeley, California, USA.
Walter E FinkbeinerDepartment of Pathology, University of California, San Francisco, California, USA.
Peter WalentekGenetics, Genomics and Development Division, Molecular and Cell Biology Department, University of California, Berkeley, California, USApeter.walentek@medizin.uni-freiburg.de.
University of California, San Francisco · USUniversity of Freiburg · DEChildren's Medical Research Institute · AUInstitut thématique Génétique, génomique et bioinformatique · FRUniversity Medical Center Freiburg · DE

Funding

SynthesisP30DK072517 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI VERKMAN, ALAN S · 2005 to 2022
$18.1M
Gene Expression in Amphibian DevlopementR01GM042341 · NIGMS · UNIVERSITY OF CALIFORNIA BERKELEY · PI HARLAND, RICHARD M · 1988 to 2016
$5.7M
Molecular mechanisms of mucociliary function and airway clearanceK99HL127275 · NHLBI · UNIVERSITY OF CALIFORNIA BERKELEY · PI WALENTEK, PETER · 2016 to 2017
$268k
NHLBI NIH HHS K99 HL127275NIDDK NIH HHS P30 DK072517NIGMS NIH HHS R01 GM042341
6 · The paper itself

Abstract

Na+/H+ exchangers (NHEs) represent a highly conserved family of ion transporters that regulate pH homeostasis. NHEs as well as other proton transporters were previously linked to the regulation of the Wnt signaling pathway, cell polarity signaling, and mucociliary function. Furthermore, mutations in the gene SLC9A3 (encoding NHE3) were detected as additional risk factors for airway infections in cystic fibrosis patients. Here, we used the Xenopus embryonic mucociliary epidermis as well as human airway epithelial cells (HAECs) as models to investigate the functional roles of NHEs in mucociliary development and regeneration. In Xenopus embryos, NHEs 1-3 were expressed during epidermal development, and loss of NHE function impaired mucociliary clearance in tadpoles. Clearance defects were caused by reduced cilia formation, disrupted alignment of basal bodies in multiciliated cells (MCCs), and dysregulated mucociliary gene expression. These data also suggested that NHEs may contribute to the activation of Wnt signaling in mucociliary epithelia. In HAECs, pharmacological inhibition of NHE function also caused defective ciliation and regeneration in airway MCCs. Collectively, our data revealed a requirement for NHEs in vertebrate mucociliary epithelia and linked NHE activity to cilia formation and function in differentiating MCCs. Our results provide an entry point for the understanding of the contribution of NHEs to signaling, development, and pathogenesis in the human respiratory tract.

Indexed as

AnimalsCells, CulturedEpitheliumHumansSodium-Hydrogen Exchanger 3Sodium-Hydrogen ExchangersWnt Signaling PathwayXenopusSodium-Hydrogen Exchanger 3Sodium-Hydrogen ExchangersAirwayCiliaNa+/H+ exchangersSlc9a1Slc9a2Slc9a3Xenopus

Identifiers

PMID30300884
PMCPMC6397095
OpenAlexW2898035156

What OpenQuestion holds

Textmetadata
LicenceTDM
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.