Evidence map›Paper›PMID 25995473›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2015

Selective deletion of cochlear hair cells causes rapid age-dependent changes in spiral ganglion and cochlear nucleus neurons.

Ling Tong, Melissa K Strong, Tejbeer Kaur, Jose M Juiz, Elizabeth C Oesterle, Clifford Hume, Mark E Warchol, Richard D Palmiter, Edwin W Rubel

Open access · hybridAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
3.4field-weighted citation impact, top 8% 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

55 citing papers in PubMed, 90 citations in OpenAlex.

  1. Article
  2. Article
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  4. Infrared light stimulates the cochlea through a mechanical displacement detected and amplified by hair cells.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  5. Article
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  7. Review
  8. Article
  9. The transcription factorFrontiers in cellular neuroscience · 2024
    Article
  10. Article
  11. Article
  12. Single-cell transcriptomic profiling of the mouse cochlea: An atlas for targeted therapies.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  13. Article
  14. Article
  15. Article
  16. Cochlear Health and Cochlear-implant Function.Journal of the Association for Research in Otolaryngology : JARO · 2023
    Review
  17. Article
  18. Article
  19. Article
  20. Repair of surviving hair cells in the damaged mouse utricle.Proceedings of the National Academy of Sciences of the United States of America · 2022
    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 5 institutions in 2 countries.

Ling TongVirginia Merrill Bloedel Hearing Research Center, Department of Otolaryngology-Head and Neck Surgery.
Melissa K StrongVirginia Merrill Bloedel Hearing Research Center, Department of Otolaryngology-Head and Neck Surgery.
Tejbeer KaurDepartment of Otolaryngology, Washington University School of Medicine, St. Louis, Missouri 63110.
Jose M JuizDiscapacidades Neurológicas and School of medicine, Universidad de Castilla-La Mancha, 02008 Albacete, Spain, and.
Elizabeth C OesterleVirginia Merrill Bloedel Hearing Research Center, Department of Otolaryngology-Head and Neck Surgery.
Clifford HumeVirginia Merrill Bloedel Hearing Research Center, Department of Otolaryngology-Head and Neck Surgery.
Mark E WarcholDepartment of Otolaryngology, Washington University School of Medicine, St. Louis, Missouri 63110.
Richard D PalmiterDepartment of Biochemistry and Howard Hughes Medical Institute, and.ORCID http://orcid.org/0000-0001-6587-0582
Edwin W RubelVirginia Merrill Bloedel Hearing Research Center, Department of Otolaryngology-Head and Neck Surgery, Department of Physiology and Biophysics, University of Washington, Seattle, Washington 98195, rubel@uw.edu.ORCID http://orcid.org/0000-0002-7265-0411
Merrill (United States) · USWashington University in St. Louis · USHoward Hughes Medical Institute · USUniversity of Castilla-La Mancha · ESUniversity of Washington · US

Funding

UNIVERSITY OF WASHINGTON RESEARCH CORE CENTERP30DC004661 · NIDCD · UNIVERSITY OF WASHINGTON · PI RAIBLE, DAVID W, STONE, JENNIFER S. · 2000 to 2014
$11.1M
Auditory Neuroscience Traning ProgramT32DC005361 · NIDCD · UNIVERSITY OF WASHINGTON · PI Adrian KC Lee, DAVID J PERKEL · 2002 to 2026
$8.8M
Sensory Function CoreP30DC004665 · NIDCD · WASHINGTON UNIVERSITY · PI FADDIS, BRIAN T · 2001 to 2015
$8.0M
Intellectual and Developmental Disabilities Research CenterU54HD083091 · NICHD · UNIVERSITY OF WASHINGTON · PI DOHERTY, DANIEL · 2014 to 2019
$7.9M
MECHANISMS OF SENSORY REGENERATIONR01DC006283 · NIDCD · WASHINGTON UNIVERSITY · PI WARCHOL, MARK · 2004 to 2025
$6.8M
Motley Diversity SupplementR01DC003829 · NIDCD · UNIVERSITY OF WASHINGTON · PI RUBEL, EDWIN W · 1999 to 2014
$6.0M
NRSA Training CoreTL1TR001415 · NCATS · UNIVERSITY OF CALIFORNIA-IRVINE · PI CAIOZZO, VINCENT JAMES, HEAD, ELIZABETH · 2015 to 2023
$4.2M
NCATS NIH HHS TL1 TR001415NICHD NIH HHS U54 HD083091NIDCD NIH HHS DC006283NIDCD NIH HHS DC03829NIDCD NIH HHS DC04661NIDCD NIH HHS DC04665NIDCD NIH HHS P30 DC004661NIDCD NIH HHS P30 DC004665NIDCD NIH HHS R01 DC003829NIDCD NIH HHS R01 DC006283NIDCD NIH HHS T32 DC005361
6 · The paper itself

Abstract

During nervous system development, critical periods are usually defined as early periods during which manipulations dramatically change neuronal structure or function, whereas the same manipulations in mature animals have little or no effect on the same property. Neurons in the ventral cochlear nucleus (CN) are dependent on excitatory afferent input for survival during a critical period of development. Cochlear removal in young mammals and birds results in rapid death of target neurons in the CN. Cochlear removal in older animals results in little or no neuron death. However, the extent to which hair-cell-specific afferent activity prevents neuronal death in the neonatal brain is unknown. We further explore this phenomenon using a new mouse model that allows temporal control of cochlear hair cell deletion. Hair cells express the human diphtheria toxin (DT) receptor behind the Pou4f3 promoter. Injections of DT resulted in nearly complete loss of organ of Corti hair cells within 1 week of injection regardless of the age of injection. Injection of DT did not influence surrounding supporting cells directly in the sensory epithelium or spiral ganglion neurons (SGNs). Loss of hair cells in neonates resulted in rapid and profound neuronal loss in the ventral CN, but not when hair cells were eliminated at a more mature age. In addition, normal survival of SGNs was dependent on hair cell integrity early in development and less so in mature animals. This defines a previously undocumented critical period for SGN survival.

Indexed as

AnimalsCell DeathCochlear NucleusDiphtheria ToxinHair Cells, AuditoryHearingHeparin-binding EGF-like Growth FactorMiceMice, Inbred C57BLMice, Inbred CBASpiral GanglionDiphtheria ToxinHeparin-binding EGF-like Growth Factorcochleacochlear nucleuscritical perioddiphtheria toxin receptor knock-inneuronal deathspiral ganglion

Identifiers

PMID25995473
PMCPMC4438131
OpenAlexW1514449661

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.