Evidence map›Paper›PMID 25385613›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2014

Spontaneous regeneration of cochlear supporting cells after neonatal ablation ensures hearing in the adult mouse.

Marcia M Mellado Lagarde, Guoqiang Wan, LingLi Zhang, Angelica R Gigliello, John J McInnis, Yingxin Zhang, Dwight Bergles, Jian Zuo, Gabriel Corfas

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

52 citing papers in PubMed, 68 citations in OpenAlex.

  1. Article
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  8. Extracellular vesicles for developing targeted hearing loss therapy.Journal of controlled release : official journal of the Controlled Release Society · 2024
    Review
  9. Hair Cell Regeneration: From Animals to Humans.Clinical and experimental otorhinolaryngology · 2024
    Review
  10. Review
  11. Article
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  14. Article
  15. Article
  16. Article
  17. Cochlear Development; New Tools and Approaches.Frontiers in cell and developmental biology · 2022
    Review
  18. Article
  19. 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

9 authors at 6 institutions in 2 countries.

Marcia M Mellado LagardeDepartment of Developmental Neurobiology, St. Jude Children's Research Hospital, Memphis, TN 38105; Hearing Research Group, School of Pharmacy and Biomolecular Sciences, University of Brighton, Brighton BN2 4GJ, United Kingdom;
Guoqiang WanF. M. Kirby Neurobiology Center, Children's Hospital Boston, Harvard Medical School, Boston, MA 02115; Departments of Neurology and Kresge Hearing Research Institute, Department of Otolaryngology-Head and Neck Surgery, University of Michigan, Ann Arbor, MI 48109; and.
LingLi ZhangDepartment of Developmental Neurobiology, St. Jude Children's Research Hospital, Memphis, TN 38105;
Angelica R GiglielloF. M. Kirby Neurobiology Center, Children's Hospital Boston, Harvard Medical School, Boston, MA 02115;
John J McInnisF. M. Kirby Neurobiology Center, Children's Hospital Boston, Harvard Medical School, Boston, MA 02115;
Yingxin ZhangSolomon H. Snyder Department of Neuroscience, John Hopkins University School of Medicine, Baltimore, MD 21205.
Dwight BerglesSolomon H. Snyder Department of Neuroscience, John Hopkins University School of Medicine, Baltimore, MD 21205.
Jian ZuoDepartment of Developmental Neurobiology, St. Jude Children's Research Hospital, Memphis, TN 38105; jian.zuo@stjude.org corfas@med.umich.edu.
Gabriel CorfasF. M. Kirby Neurobiology Center, Children's Hospital Boston, Harvard Medical School, Boston, MA 02115; Departments of Neurology and Kresge Hearing Research Institute, Department of Otolaryngology-Head and Neck Surgery, University of Michigan, Ann Arbor, MI 48109; and Otology and Laryngology, Harvard Medical School, Boston, MA 02115; jian.zuo@stjude.org corfas@med.umich.edu.
Boston Children's Hospital · USHarvard University · USSt. Jude Children's Research Hospital · USJohns Hopkins Medicine · USJohns Hopkins University · USUniversity of Brighton · GB

Funding

Viral Vector Technology (VVTSR)P30CA021765 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI CHARLES ROBERTS · 1985 to 2026
$166.9M
SYNAPTIC MECHANISMS IN HIPPOCAMPAL EPILEPTOGENESISP30HD018655 · NICHD · CHILDREN'S HOSPITAL BOSTON · PI POMEROY, SCOTT LOREN · 1985 to 2015
$26.2M
Trophic Interactions in the Developing and Adult Inner EarR01DC004820 · NIDCD · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI CORFAS, GABRIEL · 2002 to 2019
$6.2M
GENETIC ANALYSIS OF MAMMALIAN HEARING SENSITIVITYR01DC006471 · NIDCD · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI ZUO, JIAN · 2004 to 2013
$3.5M
Drug discovery for hair cell regeneration in adult mammalian cochleaeR21DC013879 · NIDCD · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI ZUO, JIAN · 2014 to 2015
$479k
NCI NIH HHS P30 CA021765NCI NIH HHS P30CA21765NICHD NIH HHS P30 HD018655NICHD NIH HHS P30 HD18655NIDCD NIH HHS DC006471NIDCD NIH HHS R01 DC004820NIDCD NIH HHS R01DC004820NIDCD NIH HHS R01 DC006471NIDCD NIH HHS R21 DC013879Wellcome Trust 08915
6 · The paper itself

Abstract

Supporting cells in the cochlea play critical roles in the development, maintenance, and function of sensory hair cells and auditory neurons. Although the loss of hair cells or auditory neurons results in sensorineural hearing loss, the consequence of supporting cell loss on auditory function is largely unknown. In this study, we specifically ablated inner border cells (IBCs) and inner phalangeal cells (IPhCs), the two types of supporting cells surrounding inner hair cells (IHCs) in mice in vivo. We demonstrate that the organ of Corti has the intrinsic capacity to replenish IBCs/IPhCs effectively during early postnatal development. Repopulation depends on the presence of hair cells and cells within the greater epithelial ridge and is independent of cell proliferation. This plastic response in the neonatal cochlea preserves neuronal survival, afferent innervation, and hearing sensitivity in adult mice. In contrast, the capacity for IBC/IPhC regeneration is lost in the mature organ of Corti, and consequently IHC survival and hearing sensitivity are impaired significantly, demonstrating that there is a critical period for the regeneration of cochlear supporting cells. Our findings indicate that the quiescent neonatal organ of Corti can replenish specific supporting cells completely after loss in vivo to guarantee mature hearing function.

Indexed as

HearingRegenerationAnimalsAnimals, NewbornCochleaMicecell ablationdeafnessgliahair cellorgan of Corti

Identifiers

PMID25385613
PMCPMC4250150
OpenAlexW2045653118

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.