Evidence map›Paper›PMID 23318633›Full record

ArticleDevelopmental biology2013

The Atoh1-lineage gives rise to hair cells and supporting cells within the mammalian cochlea.

Elizabeth Carroll Driver, Laura Sillers, Thomas M Coate, Matthew F Rose, Matthew W Kelley

Open access · greenAbstract read
In one paragraph

Article in Developmental biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 99 papers.

0numbers the graph read from it
0cells of the map it votes in
99citing papers in PubMed
6.2field-weighted citation impact, top 2% 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

99 citing papers in PubMed, 142 citations in OpenAlex.

  1. Article
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  6. Retinoic acid receptor assembly dynamics governs dual functions in cochlear organogenesis.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  7. Article
  8. Sponge bHLH Gene Expression inInternational journal of molecular sciences · 2025
    Article
  9. Article
  10. Long-rangeProceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  11. Article
  12. Revisiting the Potency of Tbx2 Expression in Transforming Outer Hair Cells into Inner Hair Cells at Multiple Ages In Vivo.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
  13. Article
  14. Review
  15. Fgf8Neuroscience bulletin · 2023
    Article
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  18. Review
  19. Article
  20. Dispensable role of Rac1 and Rac3 after cochlear hair cell specification.Journal of molecular medicine (Berlin, Germany) · 2023
    Article

39 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

5 authors at 2 institutions in 1 country.

Elizabeth Carroll DriverLaboratory of Cochlear Development, National Institute on Deafness and Other Communications Disorders, NIH, Bethesda, MD 20892, USA. drivere@nidcd.nih.gov
Laura Sillers
Thomas M Coate
Matthew F Rose
Matthew W Kelley
National Institute on Deafness and Other Communication Disorders · USBaylor College of Medicine · US

Funding

Hair Cell Development in the Mammalian CochleaZIADC000059 · NIDCD · NATIONAL INSTITUTE ON DEAFNESS AND OTHER COMMUNICATION DISORDERS · PI KELLEY, MATTHEW · 2009 to 2025
$41.8M
Howard Hughes Medical InstituteIntramural NIH HHS Z99 CL999999Intramural NIH HHS Z99 DA999999Intramural NIH HHS Z99 DC999999Intramural NIH HHS Z99 OD999999Intramural NIH HHS ZIA DC000059
6 · The paper itself

Abstract

The organ of Corti, located within the mammalian cochlea, contains a precise mosaic of hair cells (HC) and supporting cells (SC), the patterning of which is critical for auditory function. Progenitors of HCs and SCs are found in the same post-mitotic region of the cochlear duct during early stages of cochlear development, and both HCs and SCs are absent in mice lacking the transcription factor Atoh1. Based on existing data, Atoh1 is thought to be the earliest determinant of HC fate, and to have a cell-autonomous role in HC differentiation, but the lineage of Atoh1-positive cells within the cochlear duct remains unclear. To address this issue, we used an inducible Atoh1(Cre⁎PR) allele to permanently mark Atoh1-expressing cells at different developmental time points. We found that up to 30% of cells from the Atoh1-lineage develop as SCs, and that the number of Atoh1-positive SCs decreases both spatially and temporally in a pattern consistent with ongoing commitment. Modulation of Notch signaling, necessary for formation of the HC-SC mosaic, changes the percentage of cells from the Atoh1-lineage that develop as either HCs or SCs. The HC-SC ratio is also affected by morphogenesis of the cochlea, as inhibiting the outgrowth of the cochlear duct increases the number of Atoh1-lineage cells that develop as SCs. Our results demonstrate that the Atoh1-lineage is established early in cochlear development, but also show that expression of Atoh1 does not absolutely result in commitment to a HC fate.

Indexed as

Age FactorsAnalysis of VarianceAnimalsBasic Helix-Loop-Helix ProteinsCell DifferentiationCochleaGene Expression ProfilingGene Expression Regulation, DevelopmentalHair Cells, AuditoryImmunohistochemistryLabyrinth Supporting CellsMiceReceptors, NotchSignal TransductionAtoh1 protein, mouseBasic Helix-Loop-Helix ProteinsReceptors, Notch

Identifiers

PMID23318633
PMCPMC3652277
OpenAlexW2064465610

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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.