Evidence map›Paper›PMID 24466234›Full record

ArticlePloS one2014

Matrix metalloproteinase-20 over-expression is detrimental to enamel development: a Mus musculus model.

Masashi Shin, Yuanyuan Hu, Coralee E Tye, Xiaomu Guan, Craig C Deagle, Jerry V Antone, Charles E Smith, James P Simmer, John D Bartlett

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

16 citing papers in PubMed, 25 citations in OpenAlex.

  1. Integrative multi-omics and bioinformatic analysis ofThe Japanese dental science review · 2026
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  16. Maturation stage enamel malformations in Amtn and Klk4 null mice.Matrix biology : journal of the International Society for Matrix Biology
    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

9 authors at 3 institutions in 2 countries.

Masashi ShinDepartment of Mineralized Tissue Biology and Harvard School of Dental Medicine, The Forsyth Institute, Cambridge Massachusetts, United States of America.
Yuanyuan HuDepartment of Biologic and Materials Sciences, University of Michigan School of Dentistry, Ann Arbor, Michigan, United States of America.
Coralee E TyeDepartment of Mineralized Tissue Biology and Harvard School of Dental Medicine, The Forsyth Institute, Cambridge Massachusetts, United States of America.
Xiaomu GuanDepartment of Mineralized Tissue Biology and Harvard School of Dental Medicine, The Forsyth Institute, Cambridge Massachusetts, United States of America.
Craig C DeagleProgram in Endodontics, Harvard School of Dental Medicine, Boston Massachusetts, United States of America.
Jerry V AntoneDepartment of Mineralized Tissue Biology and Harvard School of Dental Medicine, The Forsyth Institute, Cambridge Massachusetts, United States of America.
Charles E SmithDepartment of Biologic and Materials Sciences, University of Michigan School of Dentistry, Ann Arbor, Michigan, United States of America ; Facility for Electron Microscopy Research, Department of Anatomy & Cell Biology, and Faculty of Dentistry, McGill University, Montreal, QC, Canada.
James P SimmerDepartment of Biologic and Materials Sciences, University of Michigan School of Dentistry, Ann Arbor, Michigan, United States of America.
John D BartlettDepartment of Mineralized Tissue Biology and Harvard School of Dental Medicine, The Forsyth Institute, Cambridge Massachusetts, United States of America.
University of Michigan–Ann Arbor · USHarvard University · USMichigan United · US

Funding

Enamelysin Processing Mechanisms in AmelogenesisR01DE016276 · NIDCR · OHIO STATE UNIVERSITY · PI BARTLETT, JOHN D · 2006 to 2014
$4.4M
Functional Studies of Kallikrein 4R01DE019775 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SIMMER, JAMES P · 2009 to 2013
$1.8M
MicroCT Core Facility in the Forsyth InstituteS10RR027553 · NCRR · ADA FORSYTH INSTITUTE, INC. · PI SASAKI, HAJIME · 2010 to 2010
$295k
NCRR NIH HHS 1S10RR027553-01NCRR NIH HHS S10 RR027553NIDCR NIH HHS R01 DE016276NIDCR NIH HHS R01DE016276NIDCR NIH HHS R01 DE019775NIDCR NIH HHS R01DE019775
6 · The paper itself

Abstract

backgroundMatrix metalloproteinase-20 (Mmp20) ablated mice have enamel that is thin and soft with an abnormal rod pattern that abrades from the underlying dentin. We asked if introduction of transgenes expressing Mmp20 would revert this Mmp20 null phenotype back to normal. Unexpectedly, for transgenes expressing medium or high levels of Mmp20, we found opposite enamel phenotypes depending on the genetic background (Mmp20(-/-) or Mmp20(+/+) ) in which the transgenes were expressed. METHODOLOGY/PRINCIPAL

findingsAmelx-promoter-Mmp20 transgenic founder mouse lines were assessed for transgene expression and those expressing low, medium or high levels of Mmp20 were selected for breeding into the Mmp20 null background. Regardless of expression level, each transgene brought the null enamel back to full thickness. However, the high and medium expressing Mmp20 transgenes in the Mmp20 null background had significantly harder more mineralized enamel than did the low transgene expresser. Strikingly, when the high and medium expressing Mmp20 transgenes were present in the wild-type background, the enamel was significantly less well mineralized than normal. Protein gel analysis of enamel matrix proteins from the high and medium expressing transgenes present in the wild-type background demonstrated that greater than normal amounts of cleavage products and smaller quantities of higher molecular weight proteins were present within their enamel matrices. CONCLUSIONS/SIGNIFICANCE: Mmp20 expression levels must be within a specific range for normal enamel development to occur. Creation of a normally thick enamel layer may occur over a wider range of Mmp20 expression levels, but acquisition of normal enamel hardness has a narrower range. Since over-expression of Mmp20 results in decreased enamel hardness, this suggests that a balance exists between cleaved and full-length enamel matrix proteins that are essential for formation of a properly hardened enamel layer. It also suggests that few feedback controls are present in the enamel matrix to prevent excessive MMP20 activity.

Indexed as

AmelogeninAnimalsBlotting, WesternDental EnamelDental Enamel ProteinsFemaleHardnessHumansMaleMatrix Metalloproteinase 20MiceMice, Inbred C57BLMice, TransgenicMicroscopy, Electron, ScanningModels, AnimalPhenotypeAmelogeninAmelx protein, mouseDental Enamel Proteinsenamel matrix proteinsMatrix Metalloproteinase 20Mmp20 protein, mouseRNA, Messenger

Identifiers

PMID24466234
PMCPMC3900650
OpenAlexW2124840971

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.