Evidence map›Paper›PMID 23415939›Full record

ArticleJournal of theoretical biology2013

A mechanochemical model for auto-regulation of lung airway surface layer volume.

Gregory Herschlag, Guilherme J M Garcia, Brian Button, Robert Tarran, Brandon Lindley, Benjamin Reinhardt, Timothy C Elston, M Gregory Forest

Abstract read
In one paragraph

Article in Journal of theoretical biology, 2013. 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
1.2field-weighted citation impact, top 18% 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, 16 citations in OpenAlex.

  1. Metachrony drives effective mucociliary transport via a calcium-dependent mechanism.American journal of physiology. Lung cellular and molecular physiology · 2024
    Article
  2. Article
  3. TheThe European respiratory journal · 2018
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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

8 authors at 5 institutions in 2 countries.

Gregory HerschlagDepartment of Mathematics, University of North Carolina, Chapel Hill, NC, USA. gregoryh@unc.edu
Guilherme J M Garcia
Brian Button
Robert Tarran
Brandon Lindley
Benjamin Reinhardt
Timothy C Elston
M Gregory Forest
University of North Carolina at Chapel Hill · USCornell University · USFederal University of São João del-Rei · BRUnited States Naval Research Laboratory · USUniversity of North Carolina Health Care · US

Funding

Virtual Lung Project: Integrated Modeling of EpithelialR01HL077546 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SUPERFINE, RICHARD · 2006 to 2010
$3.6M
SPLUNC1-Derived Peptides as ENaC AntagonistsR01HL108927 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI TARRAN, ROBERT · 2012 to 2015
$1.4M
Computational and Cell Culture Models for Mucus ClearanceRC1ES018686 · NIEHS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SUPERFINE, RICHARD · 2009 to 2010
$972k
NHLBI NIH HHS HL108927NHLBI NIH HHS R01 HL077546NHLBI NIH HHS R01HL077546-0105NHLBI NIH HHS R01 HL108927NIEHS NIH HHS 5-RC1-ES018686-01-02NIEHS NIH HHS RC1 ES018686
6 · The paper itself

Abstract

We develop a proof-of-principle model for auto-regulation of water volume in the lung airway surface layer (ASL) by coupling biochemical kinetics, transient ASL volume, and homeostatic mechanical stresses. The model is based on the hypothesis that ASL volume is sensed through soluble mediators and phasic stresses generated by beating cilia and air drag forces. Model parameters are fit based on the available data on human bronchial epithelial cell cultures. Simulations then demonstrate that homeostatic volume regulation is a natural consequence of the processes described. The model maintains ASL volume within a physiological range that modulates with phasic stress frequency and amplitude. Next, we show that the model successfully reproduces the responses of cell cultures to significant isotonic and hypotonic challenges, and to hypertonic saline, an effective therapy for mucus hydration in cystic fibrosis patients. These results compel an advanced airway hydration model with therapeutic value that will necessitate detailed kinetics of multiple molecular pathways, feedback to ASL viscoelasticity properties, and stress signaling from the ASL to the cilia and epithelial cells.

Indexed as

Models, BiologicalBody WaterCiliaElasticityHomeostasisHumansLungMucusRespiratory MucosaStress, MechanicalViscosity

Identifiers

PMID23415939
PMCPMC3631568
OpenAlexW2165139790

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.