Evidence map›Paper›PMID 20056713›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2010

An EGFR autocrine loop encodes a slow-reacting but dominant mode of mechanotransduction in a polarized epithelium.

Nikola Kojic, Euiheon Chung, Alvin T Kho, Jin-Ah Park, Austin Huang, Peter T C So, Daniel J Tschumperlin

Abstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
–field-weighted citation impact
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

16 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Airway mechanical compression: its role in asthma pathogenesis and progression.European respiratory review : an official journal of the European Respiratory Society · 2020
    Review
  5. Article
  6. Cell Jamming in the Airway Epithelium.Annals of the American Thoracic Society · 2016
    Review
  7. Article
  8. Coming to terms with tissue engineering and regenerative medicine in the lung.American journal of physiology. Lung cellular and molecular physiology · 2015
    Review
  9. Putting the Squeeze on Airway Epithelia.Physiology (Bethesda, Md.) · 2015
    Review
  10. Article
  11. miR-146a regulates mechanotransduction and pressure-induced inflammation in small airway epithelium.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2012
    Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. 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.

Nikola KojicDivision of Health Sciences and Technology, Harvard-Massachusetts Institute of Technology, Cambridge, Massachusetts, USA.
Euiheon Chung
Alvin T Kho
Jin-Ah Park
Austin Huang
Peter T C So
Daniel J Tschumperlin

Funding

Progenitor Cells inHuman Skeletal MuscleP01NS040828 · NINDS · CHILDREN'S HOSPITAL BOSTON · PI GUSSONI, EMANUELA · 2001 to 2007
$8.6M
Progenitor Cells inHuman Skeletal MuscleP50NS040828 · NINDS · BOSTON CHILDREN'S HOSPITAL · PI KOHANE, ISAAC S. · 2008 to 2011
$5.9M
Mechanical Stress as a Stimulus for Airway RemodelingR01HL088028 · NHLBI · HARVARD SCHOOL OF PUBLIC HEALTH · PI DRAZEN, JEFFREY MARK · 2007 to 2011
$2.0M
Transduction of the environment in airway epitheliumR01HL082856 · NHLBI · HARVARD SCHOOL OF PUBLIC HEALTH · PI TSCHUMPERLIN, DANIEL J. · 2006 to 2009
$1.4M
A Developmental Basis for Chronic Obstructive Lung DiseaseK25HL091124 · NHLBI · BOSTON CHILDREN'S HOSPITAL · PI KHO, ALVIN THONG-JUAK · 2008 to 2012
$743k
NHLBI NIH HHS HL082856NHLBI NIH HHS HL88028NHLBI NIH HHS K25 HL091124NHLBI NIH HHS R01 HL082856NHLBI NIH HHS R01 HL088028NINDS NIH HHS NS040828NINDS NIH HHS P01 NS040828NINDS NIH HHS P50 NS040828
6 · The paper itself

Abstract

The mechanical landscape in biological systems can be complex and dynamic, with contrasting sustained and fluctuating loads regularly superposed within the same tissue. How resident cells discriminate between these scenarios to respond accordingly remains largely unknown. Here, we show that a step increase in compressive stress of physiological magnitude shrinks the lateral intercellular space between bronchial epithelial cells, but does so with strikingly slow exponential kinetics (time constant approximately 110 s). We confirm that epidermal growth factor (EGF)-family ligands are constitutively shed into the intercellular space and demonstrate that a step increase in compressive stress enhances EGF receptor (EGFR) phosphorylation with magnitude and onset kinetics closely matching those predicted by constant-rate ligand shedding in a slowly shrinking intercellular geometry. Despite the modest degree and slow nature of EGFR activation evoked by compressive stress, we find that the majority of transcriptomic responses to sustained mechanical loading require ongoing activity of this autocrine loop, indicating a dominant role for mechanotransduction through autocrine EGFR signaling in this context. A slow deformation response to a step increase in loading, accompanied by synchronous increases in ligand concentration and EGFR activation, provides one means for cells to mount a selective and context-appropriate response to a sustained change in mechanical environment.

Indexed as

Autocrine CommunicationMechanotransduction, CellularCell PolarityEpitheliumErbB ReceptorsHumansEGFR protein, humanErbB Receptors

Identifiers

PMID20056713
PMCPMC2879944

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.