Evidence map›Paper›PMID 25406311›Full record

ArticleThe Journal of biological chemistry2015

p38α MAPK is required for tooth morphogenesis and enamel secretion.

Matthew B Greenblatt, Jung-Min Kim, Hwanhee Oh, Kwang Hwan Park, Min-Kyung Choo, Yasuyo Sano, Coralee E Tye, Ziedonis Skobe, Roger J Davis, Jin Mo Park and 3 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.4field-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

19 citing papers in PubMed, 38 citations in OpenAlex.

  1. Journal of dental research · 2026
    Article
  2. Review
  3. International journal of molecular sciences · 2025
    Article
  4. Review
  5. Roles of calcium in ameloblasts during tooth development: A scoping review.Journal of Taibah University Medical Sciences · 2025
    Review
  6. Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. Calcium Sets the Clock in Ameloblasts.Frontiers in physiology · 2020
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. [Expression and function of microRNAs in enamel development].Hua xi kou qiang yi xue za zhi = Huaxi kouqiang yixue zazhi = West China journal of stomatology · 2017
    Review
  17. Article
  18. Article
  19. 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

13 authors at 6 institutions in 2 countries.

Matthew B GreenblattFrom the Department of Pathology, Brigham and Women's Hospital, Boston, Massachusetts 02115, mag3003@med.cornell.edu.
Jung-Min Kimthe Department of Pathology and Laboratory Medicine, Weill Cornell Medical College, New York, New York 10065.
Hwanhee Ohthe Department of Pathology and Laboratory Medicine, Weill Cornell Medical College, New York, New York 10065.
Kwang Hwan Parkthe Department of Pathology and Laboratory Medicine, Weill Cornell Medical College, New York, New York 10065, the Department of Microbiology, Brain Korea 21 PLUS Project for Medical Sciences and Department of Orthopaedic Surgery, Yonsei University College of Medicine, Seoul, Republic of Korea.
Min-Kyung Choothe Cutaneous Biology Research Center, Massachusetts General Hospital and Harvard Medical School, Charlestown, Massachusetts 02129.
Yasuyo Sanothe Cutaneous Biology Research Center, Massachusetts General Hospital and Harvard Medical School, Charlestown, Massachusetts 02129.
Coralee E Tyethe Department of Biochemistry, University of Vermont College of Medicine, Burlington, Vermont, 05405.
Ziedonis Skobethe Forsyth Institute, Cambridge, Massachusetts 02142.
Roger J Davisthe Howard Hughes Medical Institute and Program in Molecular Medicine, Department of Biochemistry and Molecular Biology, University of Massachusetts Medical School, Worcester, Massachusetts 01605.
Jin Mo Parkthe Cutaneous Biology Research Center, Massachusetts General Hospital and Harvard Medical School, Charlestown, Massachusetts 02129.
Marianna Beithe Department of Surgery, Massachusetts General Hospital, Shriners Burns Hospital, Harvard Medical School, Boston, Massachusetts 02115, and.
Laurie H Glimcherthe Department of Medicine, Weill Cornell Medical College, New York, New York 10065.
Jae-Hyuck Shimthe Department of Pathology and Laboratory Medicine, Weill Cornell Medical College, New York, New York 10065, jas2060@med.cornell.edu.
Cornell University · USHarvard University · USMassachusetts General Hospital · USBrigham and Women's Hospital · USUniversity of Massachusetts Chan Medical School · USUniversity of Vermont · US

Funding

Regulatory targets of p38 MAP kinase in inflammationR01AI074957 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI PARK, JIN MO · 2009 to 2013
$1.9M
NIAID NIH HHS AI074957NIAID NIH HHS R01 AI074957
6 · The paper itself

Abstract

An improved understanding of the molecular pathways that drive tooth morphogenesis and enamel secretion is needed to generate teeth from organ cultures for therapeutic implantation or to determine the pathogenesis of primary disorders of dentition (Abdollah, S., Macias-Silva, M., Tsukazaki, T., Hayashi, H., Attisano, L., and Wrana, J. L. (1997) J. Biol. Chem. 272, 27678-27685). Here we present a novel ectodermal dysplasia phenotype associated with conditional deletion of p38α MAPK in ectodermal appendages using K14-cre mice (p38α(K14) mice). These mice display impaired patterning of dental cusps and a profound defect in the production and biomechanical strength of dental enamel because of defects in ameloblast differentiation and activity. In the absence of p38α, expression of amelogenin and β4-integrin in ameloblasts and p21 in the enamel knot was significantly reduced. Mice lacking the MAP2K MKK6, but not mice lacking MAP2K MKK3, also show the enamel defects, implying that MKK6 functions as an upstream kinase of p38α in ectodermal appendages. Lastly, stimulation with BMP2/7 in both explant culture and an ameloblast cell line confirm that p38α functions downstream of BMPs in this context. Thus, BMP-induced activation of the p38α MAPK pathway is critical for the morphogenesis of tooth cusps and the secretion of dental enamel.

Indexed as

Gene Expression Regulation, DevelopmentalAmeloblastsAmelogeninAnimalsBone Morphogenetic Protein 2Bone Morphogenetic Protein 7Cell DifferentiationCell ProliferationDental EnamelIncisorIntegrin beta4MAP Kinase Kinase 3MAP Kinase Kinase 6MiceMice, TransgenicMitogen-Activated Protein Kinase 14AmelogeninAmelx protein, mouseBmp2 protein, mousebmp7 protein, mouseBone Morphogenetic Protein 2Bone Morphogenetic Protein 7Integrin beta4Map2k3 protein, mouseMap2k6 protein, mouseMAP Kinase Kinase 3MAP Kinase Kinase 6Mitogen-Activated Protein Kinase 14p21-Activated KinasesPak1 protein, mouseAmeloblastBone Morphogenetic Protein (BMP)Ectodermal DysplasiaMicrotubule-associated Protein (MAP)p38 MAPKSMAD Transcription FactorTooth Development

Identifiers

PMID25406311
PMCPMC4281732
OpenAlexW2161241085

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.