Evidence map›Paper›PMID 29345194›Full record

ArticleAmerican journal of physiology. Lung cellular and molecular physiology2018

Transient stretch induces cytoskeletal fluidization through the severing action of cofilin.

Bo Lan, Ramaswamy Krishnan, Chan Yong Park, Rodrigo A Watanabe, Ronald Panganiban, James P Butler, Quan Lu, William C Cole, Jeffrey J Fredberg

Open access · bronzeAbstract read
In one paragraph

Article in American journal of physiology. Lung cellular and molecular physiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.9field-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

17 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
  2. An Opto-Actuated Hydrogel for Cell Mechanoactuation and Real-Time Force Monitoring.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Vimentin intermediate filaments and filamentous actin form unexpected interpenetrating networks that redefine the cell cortex.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Tissue traction microscopy to quantify muscle contraction within precision-cut lung slices.American journal of physiology. Lung cellular and molecular physiology · 2020
    Article
  14. Airway smooth muscle tone increases actin filamentogenesis and contractile capacity.American journal of physiology. Lung cellular and molecular physiology · 2020
    Article
  15. Article
  16. The Aftermath of Bronchoconstriction.Journal of engineering and science in medical diagnostics and therapy · 2019
    Review
  17. Mitigation of airways responsiveness by deep inflation of the lung.Journal of applied physiology (Bethesda, Md. : 1985) · 2018
    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

9 authors at 4 institutions in 2 countries.

Bo LanDepartment of Environmental Health, Harvard T. H. Chan School of Public Health , Boston, Massachusetts.
Ramaswamy KrishnanCenter for Vascular Biology Research, Department of Emergency Medicine, Beth Israel Deaconess Medical Center , Boston, Massachusetts.
Chan Yong ParkDepartment of Environmental Health, Harvard T. H. Chan School of Public Health , Boston, Massachusetts.
Rodrigo A WatanabeDepartment of Environmental Health, Harvard T. H. Chan School of Public Health , Boston, Massachusetts.
Ronald PanganibanDepartment of Environmental Health, Harvard T. H. Chan School of Public Health , Boston, Massachusetts.
James P ButlerDepartment of Environmental Health, Harvard T. H. Chan School of Public Health , Boston, Massachusetts.
Quan LuDepartment of Environmental Health, Harvard T. H. Chan School of Public Health , Boston, Massachusetts.
William C ColeSmooth Muscle Research Group and Department of Physiology and Pharmacology, Cumming School of Medicine, University of Calgary, Alberta, Canada.
Jeffrey J FredbergDepartment of Environmental Health, Harvard T. H. Chan School of Public Health , Boston, Massachusetts.
Harvard University · USUniversity of Calgary · CABrigham and Women's Hospital · USCenter for Vascular Biology Research · US

Funding

Training Program in Molecular and Integrative Physiological SciencesT32HL007118 · NHLBI · HARVARD UNIVERSITY (SCH OF PUBLIC HLTH) · PI LU, QUAN · 1985 to 2025
$14.3M
Physics of collective cellular migration in lung health and diseaseP01HL120839 · NHLBI · HARVARD SCHOOL OF PUBLIC HEALTH · PI FREDBERG, JEFFREY J · 2014 to 2018
$12.2M
Epithelial layer jamming in breast cancer cell migrationU01CA202123 · NCI · HARVARD SCHOOL OF PUBLIC HEALTH · PI FREDBERG, JEFFREY J · 2015 to 2019
$3.4M
Mechanics of Monolayer MigrationR01HL107561 · NHLBI · HARVARD SCHOOL OF PUBLIC HEALTH · PI FREDBERG, JEFFREY J · 2011 to 2015
$3.1M
Monitoring contractile forces during airway constrictionR21HL123522 · NHLBI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI KRISHNAN, RAMASWAMY · 2016 to 2017
$492k
CIHR MOP-13505CIHR MOP-97988NCI NIH HHS U01 CA202123NHLBI NIH HHS P01 HL120839NHLBI NIH HHS R01 HL107561NHLBI NIH HHS R21 HL123522NHLBI NIH HHS T32 HL007118
6 · The paper itself

Abstract

With every deep inspiration (DI) or sigh, the airway wall stretches, as do the airway smooth muscle cells in the airway wall. In response, the airway smooth muscle cell undergoes rapid stretch-induced cytoskeletal fluidization. As a molecular mechanism underlying the cytoskeletal fluidization response, we demonstrate a key role for the actin-severing protein cofilin. Using primary human airway smooth muscle cells, we simulated a DI by imposing a transient stretch of physiological magnitude and duration. We used traction microscopy to measure the resulting changes in contractile forces. After a transient stretch, cofilin-knockdown cells exhibited a 29 ± 5% decrease in contractile force compared with prestretch conditions. By contrast, control cells exhibited a 67 ± 6% decrease ( P < 0.05, knockdown vs. control). Consistent with these contractile force changes with transient stretch, actin filaments in cofilin-knockdown cells remained largely intact, whereas actin filaments in control cells were rapidly disrupted. Furthermore, in cofilin-knockdown cells, contractile force at baseline was higher and rate of remodeling poststretch was slower than in control cells. Additionally, the severing action of cofilin was restricted to the release phase of the transient stretch. We conclude that the actin-severing activity of cofilin is an important factor in stretch-induced cytoskeletal fluidization and may account for an appreciable part of the bronchodilatory effects of a DI.

Indexed as

Actin CytoskeletonCells, CulturedCofilin 1CytoskeletonHumansMechanotransduction, CellularMuscle ContractionMyocytes, Smooth MuscleRespiratory SystemRheologyRNA, Small InterferingCofilin 1RNA, Small Interferingairway smooth musclecofilincytoskeletondeep inspirationfluidizationstretch

Identifiers

PMID29345194
PMCPMC6008132
OpenAlexW2782629689

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.