Evidence map›Paper›PMID 22956984›Full record

ArticleCellular and molecular bioengineering2010

Influence of Transmural Pressure and Cytoskeletal Structure on NF-κB Activation in Respiratory Epithelial Cells.

Yan Huang, Caroline Haas, Samir N Ghadiali

Abstract read
In one paragraph

Article in Cellular and molecular bioengineering, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.6field-weighted citation impact, top 11% 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

21 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Magnetoactive,Cellular and molecular bioengineering · 2024
    Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. The Aftermath of Bronchoconstriction.Journal of engineering and science in medical diagnostics and therapy · 2019
    Review
  9. Review
  10. Article
  11. Article
  12. Cell Jamming in the Airway Epithelium.Annals of the American Thoracic Society · 2016
    Review
  13. Putting the Squeeze on Airway Epithelia.Physiology (Bethesda, Md.) · 2015
    Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. 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
  20. 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.

Yan HuangDepartment of Biomedical Engineering, The Ohio State University, 270 Bevis Hall, 1080 Carmack Road, Columbus, OH 43210, USA.
Caroline Haas
Samir N Ghadiali
The Ohio State University · US

Funding

Testing/ImagingP50DC007667 · NIDCD · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI ALPER, CUNEYT METIN · 2006 to 2017
$12.6M
Biomechanical Evaluation of Eustachian Tube DysfunctionR01DC007230 · NIDCD · OHIO STATE UNIVERSITY · PI GHADIALI, SAMIR N · 2006 to 2010
$704k
NIDCD NIH HHS P50 DC007667NIDCD NIH HHS R01 DC007230
6 · The paper itself

Abstract

Respiratory epithelial cells are exposed to complex mechanical forces which are often modulated during pathological conditions such as Otitis Media and acute lung injury. The transduction of these mechanical forces into altered inflammatory signaling may play an important role in the persistence of disease conditions and inflammation. In this study, we investigated how static and oscillatory pressures altered the activation of NF-κB inflammatory pathways and how changes in the actin cytoskeleton influenced the mechanotransduction of pressure into NF-κB activation. An in vitro system was used to apply static and oscillatory pressures to alveolar epithelial cells cultured at an air-liquid interface. Latrunculin A and Jasplakinolide were used to alter the cytoskeleton and tight-junction structure and ELISA was used to monitor activation of NF-κB. Results indicate that both static and oscillatory pressures can activate NF-κB and that this activation is magnitude-dependent at low oscillation frequencies only. Jasplakinolide treated cells did not exhibit significant changes in normalized NF-κB activation compared to unloaded controls while Latrunculin treated cells exhibited increases in normalized NF-κB activation only at low frequency or static pressures. These results indicate that altering the actin cytoskeleton may be a useful way to mitigate the mechanotransduction of pressure forces into inflammatory signaling.

Identifiers

PMID22956984
PMCPMC3433077
OpenAlexW2020521000

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.