Evidence map›Paper›PMID 26538639›Full record

ArticleBiology open2015

Epithelial topography for repetitive tooth formation.

Marcia Gaete, Juan Manuel Fons, Elena Mădălina Popa, Lemonia Chatzeli, Abigail S Tucker

Open access · goldAbstract read
In one paragraph

Article in Biology open, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

11 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. From snapshots to movies: Understanding early tooth development in four dimensions.Developmental dynamics : an official publication of the American Association of Anatomists · 2017
    Review
  11. LGR4 is required for sequential molar development.Biochemistry and biophysics reports · 2016
    Article
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 2 countries.

Marcia GaeteDepartment of Craniofacial Development and Stem Cell Biology, King's College London, London SE1 9RT, UK Department of Anatomy, Faculty of Medicine, Pontificia Universidad Católica de Chile, Santiago 8331150, Chile mgaetec@med.puc.cl.
Juan Manuel FonsDepartment of Craniofacial Development and Stem Cell Biology, King's College London, London SE1 9RT, UK.
Elena Mădălina PopaDepartment of Craniofacial Development and Stem Cell Biology, King's College London, London SE1 9RT, UK.
Lemonia ChatzeliDepartment of Craniofacial Development and Stem Cell Biology, King's College London, London SE1 9RT, UK.
Abigail S TuckerDepartment of Craniofacial Development and Stem Cell Biology, King's College London, London SE1 9RT, UK.
King's College London · GBPontificia Universidad Católica de Chile · CL

Funding

Wellcome Trust 102889
6 · The paper itself

Abstract

During the formation of repetitive ectodermally derived organs such as mammary glands, lateral line and teeth, the tissue primordium iteratively initiates new structures. In the case of successional molar development, new teeth appear sequentially in the posterior region of the jaw from Sox2(+) cells in association with the posterior aspect of a pre-existing tooth. The sequence of molar development is well known, however, the epithelial topography involved in the formation of a new tooth is unclear. Here, we have examined the morphology of the molar dental epithelium and its development at different stages in the mouse in vivo and in molar explants. Using regional lineage tracing we show that within the posterior tail of the first molar the primordium for the second and third molar are organized in a row, with the tail remaining in connection with the surface, where a furrow is observed. The morphology and Sox2 expression of the tail retains characteristics reminiscent of the earlier stages of tooth development, such that position along the A-P axes of the tail correlates with different temporal stages. Sox9, a stem/progenitor cell marker in other organs, is expressed mainly in the suprabasal epithelium complementary with Sox2 expression. This Sox2 and Sox9 expressing molar tail contains actively proliferating cells with mitosis following an apico-basal direction. Snail2, a transcription factor implicated in cell migration, is expressed at high levels in the tip of the molar tail while E-cadherin and laminin are decreased. In conclusion, our studies propose a model in which the epithelium of the molar tail can grow by posterior movement of epithelial cells followed by infolding and stratification involving a population of Sox2(+)/Sox9(+) cells.

Indexed as

OdontogenesisOrganogenesisSox2Sox9Successional tooth development

Identifiers

PMID26538639
PMCPMC4736031
OpenAlexW2106153833

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.