Evidence map›Paper›PMID 24278477›Full record

ArticlePloS one2013

TGF-ß regulates enamel mineralization and maturation through KLK4 expression.

Andrew Cho, Naoto Haruyama, Bradford Hall, Mary Jo S Danton, Lu Zhang, Praveen Arany, David J Mooney, Yassine Harichane, Michel Goldberg, Carolyn W Gibson and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.5field-weighted citation impact, top 12% 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

20 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
  2. Review
  3. A novelFrontiers in physiology · 2026
    Article
  4. Review
  5. Article
  6. Review
  7. Frontiers in cell and developmental biology · 2022
    Article
  8. Article
  9. Article
  10. Calcium Sets the Clock in Ameloblasts.Frontiers in physiology · 2020
    Article
  11. Review
  12. Meeting report: a hard look at the state of enamel research.International journal of oral science · 2017
    Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Review
  19. Article
  20. Review
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 5 institutions in 3 countries.

Andrew ChoGene Transfer Core, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, Maryland, United States of America.
Naoto Haruyama
Bradford Hall
Mary Jo S Danton
Lu Zhang
Praveen Arany
David J Mooney
Yassine Harichane
Michel Goldberg
Carolyn W Gibson
Ashok B Kulkarni
National Institutes of Health · USHarvard University Press · USNational Institute of Dental and Craniofacial Research · USUniversité Paris Cité · FRUniversity of Pennsylvania · US

Funding

Molecular Roles of Cdk5 in Neuronal Functions and Pain SignalingZIADE000664 · NIDCR · NATIONAL INSTITUTE OF DENTAL & CRANIOFACIAL RESEARCH · PI KULKARNI, ASHOK · 2009 to 2025
$20.4M
Micromechanical Determinants of Organ Design and Engineering (SysCODE 6 of 10)RL1DE019023 · NIDCR · BOSTON CHILDREN'S HOSPITAL · PI INGBER, DONALD E · 2007 to 2011
$2.9M
Oral Wound HealingZIADE000741 · NIDCR · NATIONAL INSTITUTE OF DENTAL & CRANIOFACIAL RESEARCH · PI ARANY, PRAVEEN · 2013 to 2015
$2.0M
NIDCR NIH HHS R01DE019023-01NIDCR NIH HHS RL1 DE019023
6 · The paper itself

Abstract

Transforming growth factor-ß (TGF-ß) signaling plays an important role in regulating crucial biological processes such as cell proliferation, differentiation, apoptosis, and extracellular matrix remodeling. Many of these processes are also an integral part of amelogenesis. In order to delineate a precise role of TGF-ß signaling during amelogenesis, we developed a transgenic mouse line that harbors bovine amelogenin promoter-driven Cre recombinase, and bred this line with TGF-ß receptor II floxed mice to generate ameloblast-specific TGF-ß receptor II conditional knockout (cKO) mice. Histological analysis of the teeth at postnatal day 7 (P7) showed altered enamel matrix composition in the cKO mice as compared to the floxed mice that had enamel similar to the wild-type mice. The µCT and SEM analyses revealed decreased mineral content in the cKO enamel concomitant with increased attrition and thinner enamel crystallites. Although the mRNA levels remained unaltered, immunostaining revealed increased amelogenin, ameloblastin, and enamelin localization in the cKO enamel at the maturation stage. Interestingly, KLK4 mRNA levels were significantly reduced in the cKO teeth along with a slight increase in MMP-20 levels, suggesting that normal enamel maturation is regulated by TGF-ß signaling through the expression of KLK4. Thus, our study indicates that TGF-ß signaling plays an important role in ameloblast functions and enamel maturation.

Indexed as

AnimalsDental EnamelKallikreinsMiceMice, TransgenicReal-Time Polymerase Chain ReactionTransforming Growth Factor betaX-Ray Microtomographykallikrein 4KallikreinsTransforming Growth Factor beta

Identifiers

PMID24278477
PMCPMC3835418
OpenAlexW2123230395

What OpenQuestion holds

Textmetadata
LicenceCC0
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.