Evidence map›Paper›PMID 24107947›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2013

Ectopic expression of activated notch or SOX2 reveals similar and unique roles in the development of the sensory cell progenitors in the mammalian inner ear.

Wei Pan, Ying Jin, Jing Chen, Robbert J Rottier, Karen P Steel, Amy E Kiernan

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed
5.9field-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

63 citing papers in PubMed, 101 citations in OpenAlex.

  1. Article
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  4. The Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
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  11. Comparative assessment of Fgf's diverse roles in inner ear development: A zebrafish perspective.Developmental dynamics : an official publication of the American Association of Anatomists · 2021
    Review
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  19. Review
  20. Development (Cambridge, England) · 2020
    Article

3 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

6 authors at 4 institutions in 3 countries.

Wei PanDepartment of Ophthalmology and Department of Biomedical Genetics, University of Rochester, Rochester, New York 14642, Department of Pediatric Surgery, Erasmus MC-Sophia Children's Hospital, 3000 CA Rotterdam, the Netherlands, and Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge CB10 1SA, United Kingdom.
Ying Jin
Jing Chen
Robbert J Rottier
Karen P Steel
Amy E Kiernan
Ophthalmology Associates (United States) · USWellcome Sanger Institute · GBErasmus MC - Sophia Children’s Hospital · NLUniversity of Rochester · US

Funding

Sensory Organ Formation in the Inner EarR01DC009250 · NIDCD · UNIVERSITY OF ROCHESTER · PI KIERNAN, AMY · 2009 to 2019
$3.8M
Medical Research Council G0300212Medical Research Council MC_QA137918NIDCD NIH HHS DC009250NIDCD NIH HHS R01 DC009250Wellcome Trust 098051Wellcome Trust 100669
6 · The paper itself

Abstract

Hearing impairment or vestibular dysfunction in humans often results from a permanent loss of critical cell types in the sensory regions of the inner ear, including hair cells, supporting cells, or cochleovestibular neurons. These important cell types arise from a common sensory or neurosensory progenitor, although little is known about how these progenitors are specified. Studies have shown that Notch signaling and the transcription factor Sox2 are required for the development of these lineages. Previously we and others demonstrated that ectopic activation of Notch can direct nonsensory cells to adopt a sensory fate, indicating a role for Notch in early specification events. Here, we explore the relationship between Notch and SOX2 by ectopically activating these factors in nonsensory regions of the mouse cochlea, and demonstrate that, similar to Notch, SOX2 can specify sensory progenitors, consistent with a role downstream of Notch signaling. However, we also show that Notch has a unique role in promoting the proliferation of the sensory progenitors. We further demonstrate that Notch can only induce ectopic sensory regions within a certain time window of development, and that the ectopic hair cells display specialized stereocilia bundles similar to endogenous hair cells. These results demonstrate that Notch and SOX2 can both drive the sensory program in nonsensory cells, indicating these factors may be useful in cell replacement strategies in the inner ear.

Indexed as

AnimalsCell DifferentiationEar, InnerImmunohistochemistryMiceMice, TransgenicMicroscopy, Electron, ScanningNeural Stem CellsReceptors, NotchSignal TransductionSOXB1 Transcription FactorsReceptors, NotchSox2 protein, mouseSOXB1 Transcription Factors

Identifiers

PMID24107947
PMCPMC3792456
OpenAlexW1983443051

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.