Evidence map›Paper›PMID 23132246›Full record

ArticleDevelopment (Cambridge, England)2012

A dual function for canonical Wnt/β-catenin signaling in the developing mammalian cochlea.

Bonnie E Jacques, Chandrakala Puligilla, Rachel M Weichert, Anna Ferrer-Vaquer, Anna-Katerina Hadjantonakis, Matthew W Kelley, Alain Dabdoub

Open access · bronzeAbstract read
In one paragraph

Article in Development (Cambridge, England), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 109 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
109citing papers in PubMed, 1 pooled it
6.1field-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

109 citing papers in PubMed, 1 synthesis or guideline pooled it, 159 citations in OpenAlex.

  1. Pooled it
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  10. Wnt7b acts in concert with Wnt5a to regulate tissue elongation and planar cell polarity via noncanonical Wnt signaling.Proceedings of the National Academy of Sciences of the United States of America · 2024
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  11. Review
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  19. The Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
    Article
  20. Article

49 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 3 institutions in 1 country.

Bonnie E JacquesUniversity of California San Diego, School of Medicine, Department of Surgery, Division of Otolaryngology, La Jolla, CA 92093-0666, USA. bjacques@ucsd.edu
Chandrakala Puligilla
Rachel M Weichert
Anna Ferrer-Vaquer
Anna-Katerina Hadjantonakis
Matthew W Kelley
Alain Dabdoub
University of California, San Diego · USKettering University · USNational Institute on Deafness and Other Communication Disorders · US

Funding

VIRAL MALIGNANCYP30CA023100 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI DIANE M SIMEONE · 1985 to 2026
$124.9M
Hair Cell Development in the Mammalian CochleaZIADC000059 · NIDCD · NATIONAL INSTITUTE ON DEAFNESS AND OTHER COMMUNICATION DISORDERS · PI KELLEY, MATTHEW · 2009 to 2025
$41.8M
Regulation of hair cell determination by the Wnt/Calcium signaling pathwayR01DC011104 · NIDCD · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI DABDOUB, ALAIN · 2010 to 2012
$1.1M
NCI NIH HHS P30 CA023100NCI NIH HHS P30 CA23100NIDCD NIH HHS R01 DC011104NIDCD NIH HHS R01DC011104
6 · The paper itself

Abstract

The canonical Wnt/β-catenin signaling pathway is known to play crucial roles in organogenesis by regulating both proliferation and differentiation. In the inner ear, this pathway has been shown to regulate the size of the otic placode from which the cochlea will arise; however, direct activity of canonical Wnt signaling as well as its function during cochlear mechanosensory hair cell development had yet to be identified. Using TCF/Lef:H2B-GFP reporter mice and transfection of an independent TCF/Lef reporter construct, we describe the pattern of canonical Wnt activity in the developing mouse cochlea. We show that prior to terminal mitosis, canonical Wnt activity is high in early prosensory cells from which hair cells and support cells will differentiate, and activity becomes reduced as development progresses. Using an in vitro model we demonstrate that Wnt/β-catenin signaling regulates both proliferation and hair cell differentiation within the developing cochlear duct. Inhibition of Wnt/β-catenin signaling blocks proliferation during early mitotic phases of development and inhibits hair cell formation in the differentiating organ of Corti. Conversely, activation increases the number of hair cells that differentiate and induces proliferation in prosensory cells, causing an expansion of the Sox2-positive prosensory domain. We further demonstrate that the induced proliferation of Sox2-positive cells may be mediated by the cell cycle regulator cyclin D1. Lastly, we provide evidence that the mitotic Sox2-positive cells are competent to differentiate into hair cells. Combined, our data suggest that Wnt/β-catenin signaling has a dual function in cochlear development, regulating both proliferation and hair cell differentiation.

Indexed as

Wnt Signaling PathwayAnimalsbeta CateninCell DifferentiationCell ProliferationCochleaCyclin D1Green Fluorescent ProteinsHair Cells, AuditoryMiceMice, TransgenicOrgan Culture TechniquesOrgan of CortiOrganogenesisSOXB1 Transcription FactorsWnt Proteinsbeta CateninCyclin D1Green Fluorescent ProteinsSox2 protein, mouseSOXB1 Transcription FactorsWnt Proteins

Identifiers

PMID23132246
PMCPMC3509733
OpenAlexW2156310646

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.