Evidence map›Paper›PMID 25897778›Full record

ArticleNature communications2015

Length regulation of mechanosensitive stereocilia depends on very slow actin dynamics and filament-severing proteins.

Praveena Narayanan, Paul Chatterton, Akihiro Ikeda, Sakae Ikeda, David P Corey, James M Ervasti, Benjamin J Perrin

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 68 papers.

0numbers the graph read from it
0cells of the map it votes in
68citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

68 citing papers in PubMed, 101 citations in OpenAlex.

  1. Article
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  9. Review
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  11. Clarin-2 gene supplementation durably preserves hearing in a model of progressive hearing loss.Molecular therapy : the journal of the American Society of Gene Therapy · 2024
    Article
  12. Article
  13. Mechanisms of actin disassembly and turnover.The Journal of cell biology · 2023
    Review
  14. Review
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Review

8 more citing papers are in PubMed but not listed here.

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 2 institutions in 1 country.

Praveena NarayananDepartment of Biochemistry, Molecular Biology and Biophysics, University of Minnesota, Minneapolis, Minnesota 55455, USA.
Paul ChattertonDepartment of Biochemistry, Molecular Biology and Biophysics, University of Minnesota, Minneapolis, Minnesota 55455, USA.
Akihiro IkedaDepartment of Medical Genetics, University of Wisconsin-Madison, Madison, Wisconsin 53706, USA.
Sakae IkedaDepartment of Medical Genetics, University of Wisconsin-Madison, Madison, Wisconsin 53706, USA.
David P CoreyDepartment of Neurobiology, Harvard Medical School and Howard Hughes Medical Institute, Boston, Massachusetts 02115, USA.
James M ErvastiDepartment of Biochemistry, Molecular Biology and Biophysics, University of Minnesota, Minneapolis, Minnesota 55455, USA.
Benjamin J PerrinDepartment of Biology, Indiana University-Purdue University Indianapolis, Indianapolis, Indiana 46022, USA.
University of Minnesota · USUniversity of Wisconsin–Madison · US

Funding

Costamere Defects in Muscular DystrophiesR01AR049899 · NIAMS · UNIVERSITY OF WISCONSIN-MADISON · PI ERVASTI, JAMES M · 2005 to 2025
$8.2M
Corneal Epithelial Proliferation and Neovascularization*R01EY016108 · NEI · UNIVERSITY OF WISCONSIN-MADISON · PI IKEDA, SAKAE · 2005 to 2018
$4.6M
MOLECULAR BASIS OF INHERITED DEAFNESSR01DC002281 · NIDCD · MASSACHUSETTS GENERAL HOSPITAL · PI COREY, DAVID P · 1994 to 2018
$4.4M
Cytoskeletal dynamics in stereocilia maintenanceR03DC012354 · NIDCD · UNIVERSITY OF MINNESOTA · PI PERRIN, BENJAMIN J · 2012 to 2014
$451k
Howard Hughes Medical InstituteNEI NIH HHS R01 EY016108NEI NIH HHS R01EY016108NIAMS NIH HHS R01 AR049899NIAMS NIH HHS R01AR049899NIDCD NIH HHS R01 DC002281NIDCD NIH HHS R03 DC012354NIDCD NIH HHS R03DC12354
6 · The paper itself

Abstract

Auditory sensory hair cells depend on stereocilia with precisely regulated lengths to detect sound. Since stereocilia are primarily composed of crosslinked, parallel actin filaments, regulated actin dynamics are essential for controlling stereocilia length. Here we assessed stereocilia actin turnover by monitoring incorporation of inducibly expressed β-actin-GFP in adult mouse hair cells in vivo and by directly measuring β-actin-GFP turnover in explants. Stereocilia actin incorporation is remarkably slow and restricted to filament barbed ends in a small tip compartment, with minimal accumulation in the rest of the actin core. Shorter rows of stereocilia, which have mechanically gated ion channels, show more variable actin turnover than the tallest stereocilia, which lack channels. Finally, the proteins ADF and AIP1, which both mediate actin filament severing, contribute to stereocilia length maintenance. Altogether, the data support a model whereby stereocilia actin cores are largely static, with dynamic regulation at the tips to maintain a critical length.

Indexed as

Actin CytoskeletonActinsAnimalsCloning, MolecularGene Expression RegulationMechanotransduction, CellularMiceOrgan of CortiActins

Identifiers

PMID25897778
PMCPMC4523390
OpenAlexW2038659992

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.