Evidence map›Paper›PMID 26702830›Full record

ArticleDevelopmental cell2015

Migration of Founder Epithelial Cells Drives Proper Molar Tooth Positioning and Morphogenesis.

Jan Prochazka, Michaela Prochazkova, Wen Du, Frantisek Spoutil, Jolana Tureckova, Renee Hoch, Tomomi Shimogori, Radislav Sedlacek, John L Rubenstein, Torsten Wittmann and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Developmental cell, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

32 citing papers in PubMed, 54 citations in OpenAlex.

  1. Article
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  8. Ectopic Activation ofInternational journal of molecular sciences · 2024
    Article
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  14. Tooth number abnormality: from bench to bedside.International journal of oral science · 2023
    Review
  15. Article
  16. The conundrum of pharyngeal teeth origin: the role of germ layers, pouches, and gill slits.Biological reviews of the Cambridge Philosophical Society · 2022
    Review
  17. Article
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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

11 authors at 4 institutions in 4 countries.

Jan ProchazkaDepartment of Orofacial Sciences and Program in Craniofacial Biology, University of California, San Francisco, 513 Parnassus Avenue, San Francisco, CA 94143, USA; Laboratory of Transgenic Models of Diseases, Institute of Molecular Genetics of the ASCR, v.v.i., Prague 4 14220, Czech Republic.
Michaela ProchazkovaDepartment of Orofacial Sciences and Program in Craniofacial Biology, University of California, San Francisco, 513 Parnassus Avenue, San Francisco, CA 94143, USA; Laboratory of Transgenic Models of Diseases, Institute of Molecular Genetics of the ASCR, v.v.i., Prague 4 14220, Czech Republic.
Wen DuDepartment of Orofacial Sciences and Program in Craniofacial Biology, University of California, San Francisco, 513 Parnassus Avenue, San Francisco, CA 94143, USA; State Key Laboratory of Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, Sichuan 610041, China.
Frantisek SpoutilLaboratory of Transgenic Models of Diseases, Institute of Molecular Genetics of the ASCR, v.v.i., Prague 4 14220, Czech Republic.
Jolana TureckovaLaboratory of Transgenic Models of Diseases, Institute of Molecular Genetics of the ASCR, v.v.i., Prague 4 14220, Czech Republic.
Renee HochDepartment of Psychiatry, Nina Ireland Laboratory of Developmental Neurobiology, University of California, San Francisco, 1500 4th Street, San Francisco, CA 94143, USA.
Tomomi ShimogoriLaboratory for Molecular Mechanisms of Thalamus Development, RIKEN Brain Science Institute, 2-1 Hirosawa Wako, Saitama 351-0198, Japan.
Radislav SedlacekLaboratory of Transgenic Models of Diseases, Institute of Molecular Genetics of the ASCR, v.v.i., Prague 4 14220, Czech Republic.
John L RubensteinDepartment of Psychiatry, Nina Ireland Laboratory of Developmental Neurobiology, University of California, San Francisco, 1500 4th Street, San Francisco, CA 94143, USA.
Torsten WittmannDepartment of Cell and Tissue Biology, University of California, San Francisco, 513 Parnassus Avenue, San Francisco, CA 94143, USA.
Ophir D KleinDepartment of Orofacial Sciences and Program in Craniofacial Biology, University of California, San Francisco, 513 Parnassus Avenue, San Francisco, CA 94143, USA; Department of Pediatrics and Institute for Human Genetics, University of California, San Francisco, 513 Parnassus Avenue, San Francisco, CA 94143, USA. Electronic address: ophir.klein@ucsf.edu.
Czech Academy of Sciences, Institute of Molecular Genetics · CZUniversity of California, San Francisco · USRIKEN Center for Brain Science · JPSichuan University · CN

Funding

GENETIC STUDIES OF CORTEX STRUCTURE AND DEVELOPMENTR01NS034661 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI RUBENSTEIN, JOHN L. R. · 1996 to 2015
$4.6M
The role of Bmi1 in regulation of dental stem cellsR01DE021420 · NIDCR · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI KLEIN, OPHIR D · 2011 to 2015
$2.0M
The role of Hippo and YAP/TAZ in dental renewalR01DE024988 · NIDCR · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI KLEIN, OPHIR D · 2015 to 2016
$793k
Spinning disk confocal / FRAP microscope for quantitative live cell imagingS10RR026758 · NCRR · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI WITTMANN, TORSTEN · 2010 to 2010
$500k
Analysis of Fgf17 roles and regulation in mammalian forebrain developmentF32MH081431 · NIMH · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI HOCH, RENEE VICTORIA · 2008 to 2010
$104k
NCRR NIH HHS S10 RR026758NCRR NIH HHS S10-RR026758NIDCR NIH HHS R01 DE021420NIDCR NIH HHS R01-DE021420NIDCR NIH HHS R01 DE024988NIDCR NIH HHS R01-DE024988NIMH NIH HHS F32 MH081431NIMH NIH HHS F32-MH081431NINDS NIH HHS R01 NS034661NINDS NIH HHS R01-NS34661
6 · The paper itself

Abstract

The proper positioning of organs during development is essential, yet little is known about the regulation of this process in mammals. Using murine tooth development as a model, we have found that cell migration plays a central role in positioning of the organ primordium. By combining lineage tracing, genetic cell ablation, and confocal live imaging, we identified a migratory population of Fgf8-expressing epithelial cells in the embryonic mandible. These Fgf8-expressing progenitors furnish the epithelial cells required for tooth development, and the progenitor population migrates toward a Shh-expressing region in the mandible, where the tooth placode will initiate. Inhibition of Fgf and Shh signaling disrupted the oriented migration of cells, leading to a failure of tooth development. These results demonstrate the importance of intraepithelial cell migration in proper positioning of an initiating organ.

Indexed as

AnimalsCell MovementEpithelial CellsFibroblast Growth FactorsGene Expression Regulation, DevelopmentalMesodermMiceMolarMorphogenesisOdontogenesisToothFibroblast Growth Factors

Identifiers

PMID26702830
PMCPMC4710359
OpenAlexW2210102832

What OpenQuestion holds

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Registered trials

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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.