Evidence map›Paper›PMID 29217752›Full record

ArticleDevelopment (Cambridge, England)2018

Mapping the distribution of stem/progenitor cells across the mouse middle ear during homeostasis and inflammation.

Abigail S Tucker, Carlene J Dyer, Juan M Fons Romero, Tathyane H N Teshima, Jennifer C Fuchs, Hannah Thompson

Open access · bronzeAbstract read
In one paragraph

Article in Development (Cambridge, England), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.5field-weighted citation impact, top 22% 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

9 citing papers in PubMed, 21 citations in OpenAlex.

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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 2 institutions in 3 countries.

Abigail S TuckerCentre for Craniofacial and Regenerative Biology, Department of Craniofacial Development and Stem Cell Biology, King's College London, London SE1 9RT, UK abigail.tucker@kcl.ac.uk.ORCID 0000-0001-8871-6094
Carlene J DyerCentre for Craniofacial and Regenerative Biology, Department of Craniofacial Development and Stem Cell Biology, King's College London, London SE1 9RT, UK.
Juan M Fons RomeroCentre for Craniofacial and Regenerative Biology, Department of Craniofacial Development and Stem Cell Biology, King's College London, London SE1 9RT, UK.
Tathyane H N TeshimaCentre for Craniofacial and Regenerative Biology, Department of Craniofacial Development and Stem Cell Biology, King's College London, London SE1 9RT, UK.
Jennifer C FuchsCentre for Craniofacial and Regenerative Biology, Department of Craniofacial Development and Stem Cell Biology, King's College London, London SE1 9RT, UK.ORCID 0000-0001-8701-1228
Hannah ThompsonCentre for Craniofacial and Regenerative Biology, Department of Craniofacial Development and Stem Cell Biology, King's College London, London SE1 9RT, UK.
King's College London · GBUniversidade de São Paulo · BR

Funding

Wellcome Trust 102889/Z/13/Z
6 · The paper itself

Abstract

The middle ear epithelium is derived from neural crest and endoderm, which line distinct regions of the middle ear cavity. Here, we investigate the distribution of putative stem cell markers in the middle ear, combined with an analysis of the location of label-retaining cells (LRCs) to create a map of the middle ear mucosa. We show that proliferating cells and LRCs were associated with specific regions of the ear epithelium, concentrated in the hypotympanum at the base of the auditory bulla and around the ear drum. Sox2 was widely expressed in the endodermally derived ciliated pseudostratified epithelium of the hypotympanum. This part of the middle ear showed high levels of Wnt activity, as indicated by the expression of Axin2, a readout of Wnt signalling. Keratin 5 showed a more restricted expression within the basal cells of this region, with very little overlap between the Sox2- and keratin 5-positive epithelium, indicating that these genes mark distinct populations. Little expression of Sox2 or keratin 5 was observed in the neural crest-derived middle ear epithelium that lined the promontory, except in cases of otitis media when this epithelium underwent hyperplasia. This study lays the foundation for furthering our understanding of homeostasis and repair in the middle ear.

Indexed as

Ear, MiddleHomeostasisStem CellsWnt Signaling PathwayAnimalsAxin ProteinGene Expression RegulationKeratin-15MiceMice, TransgenicOtitis MediaSOXB1 Transcription FactorsAxin2 protein, mouseAxin ProteinKeratin-15Krt15 protein, mouseSox2 protein, mouseSOXB1 Transcription FactorsEndodermKeratin 5Label-retaining cellsNeural crestOtitis mediaSox2

Identifiers

PMID29217752
PMCPMC5825877
OpenAlexW2775087732

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.