Evidence map›Paper›PMID 25122764›Full record

ArticleThe Journal of biological chemistry2014

A pituitary homeobox 2 (Pitx2):microRNA-200a-3p:β-catenin pathway converts mesenchymal cells to amelogenin-expressing dental epithelial cells.

Thad Sharp, Jianbo Wang, Xiao Li, Huojun Cao, Shan Gao, Myriam Moreno, Brad A Amendt

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

21 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. Article
  3. miR-200a TargetsAnimals : an open access journal from MDPI · 2025
    Article
  4. Article
  5. Article
  6. Article
  7. Exploring microRNAs in craniofacial regenerative medicine.Biochemical Society transactions · 2023
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
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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

7 authors at 2 institutions in 1 country.

Thad SharpDepartment of Anatomy and Cell Biology, Carver College of Medicine, University of Iowa, Iowa City, Iowa 52242.
Jianbo WangInstitute of Biosciences and Technology, Texas A&M Health Science Center, Houston, Texas 77030, and.
Xiao LiDepartment of Anatomy and Cell Biology, Carver College of Medicine, University of Iowa, Iowa City, Iowa 52242.
Huojun CaoInstitute of Biosciences and Technology, Texas A&M Health Science Center, Houston, Texas 77030, and.
Shan GaoInstitute of Biosciences and Technology, Texas A&M Health Science Center, Houston, Texas 77030, and.
Myriam MorenoDepartment of Anatomy and Cell Biology, Carver College of Medicine, University of Iowa, Iowa City, Iowa 52242.
Brad A AmendtDepartment of Anatomy and Cell Biology, Carver College of Medicine, University of Iowa, Iowa City, Iowa 52242,; Craniofacial Anomalies Research Center, Carver College of Medicine, University of Iowa, Iowa City, Iowa 52242. Electronic address: brad-amendt@uiowa.edu.
University of Iowa · USTexas A&M Health Science Center · US

Funding

Molecular Mechanisms of PITX2 During Craniofacial DevelopmentR01DE013941 · NIDCR · UNIVERSITY OF TULSA · PI AMENDT, BRAD A · 2000 to 2013
$4.2M
NIDCR NIH HHS DE13941NIDCR NIH HHS R01 DE013941
6 · The paper itself

Abstract

Pitx2, Wnt/β-catenin signaling, and microRNAs (miRs) play a critical role in the regulation of dental stem cells during embryonic development. In this report, we have identified a Pitx2:β-catenin regulatory pathway involved in epithelial cell differentiation and conversion of mesenchymal cells to amelogenin expressing epithelial cells via miR-200a. Pitx2 and β-catenin are expressed in the labial incisor cervical loop or epithelial stem cell niche, with decreased expression in the differentiating ameloblast cells of the mouse lower incisor. Bioinformatics analyses reveal that miR-200a-3p expression is activated in the pre-ameloblast cells to enhance epithelial cell differentiation. We demonstrate that Pitx2 activates miR-200a-3p expression and miR-200a-3p reciprocally represses Pitx2 and β-catenin expression. Pitx2 and β-catenin interact to synergistically activate gene expression during odontogenesis and miR-200a-3p attenuates their expression and directs differentiation. To understand how this mechanism controls cell differentiation and cell fate, oral epithelial and odontoblast mesenchymal cells were reprogrammed by a two-step induction method using Pitx2 and miR-200a-3p. Conversion to amelogenin expressing dental epithelial cells involved an up-regulation of the stem cell marker Sox2 and proliferation genes and decreased expression of mesenchymal markers. E-cadherin expression was increased as well as ameloblast specific factors. The combination of Pitx2, a regulator of dental stem cells and miR-200a converts mesenchymal cells to a fully differentiated dental epithelial cell type. This pathway and reprogramming can be used to reprogram mesenchymal or oral epithelial cells to dental epithelial (ameloblast) cells, which can be used in tissue repair and regeneration studies.

Indexed as

AmelogeninAnimalsbeta CateninCell DifferentiationEpithelial CellsHomeobox Protein PITX2Homeodomain ProteinsHumansIncisorMesenchymal Stem CellsMiceMice, TransgenicMicroRNAsSOXB1 Transcription FactorsTranscription FactorsAmelogeninbeta CateninHomeobox Protein PITX2Homeodomain ProteinsMicroRNAsMIRN200 microRNA, humanMirn200 microRNA, mouseSOX2 protein, humanSox2 protein, mouseSOXB1 Transcription FactorsTranscription FactorsBeta-catenin (B-catenin)Epithelial-Mesenchymal Transition (EMT)Gene ExpressionMicroRNA (miRNA)Paired-like Homeodomain Transcription Factor 2 (PITX2)Reprogramming

Identifiers

PMID25122764
PMCPMC4175363
OpenAlexW2049845899

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.