Evidence map›Paper›PMID 28824442›Full record

ReviewFrontiers in physiology2017

Endocytosis and Enamel Formation.

Cong-Dat Pham, Charles E Smith, Yuanyuan Hu, Jan C-C Hu, James P Simmer, Yong-Hee P Chun

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in physiology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

18 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Review
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  4. Review
  5. Review
  6. Review
  7. Review
  8. Article
  9. Article
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  11. Article
  12. Article
  13. Enamel defects in Acp4Scientific reports · 2022
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. 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

6 authors at 2 institutions in 2 countries.

Cong-Dat PhamDepartment of Periodontics, School of Dentistry, University of Texas Health Science Center at San AntonioSan Antonio, TX, United States.
Charles E SmithDepartment of Anatomy and Cell Biology, McGill UniversityMontreal, QC, Canada.
Yuanyuan HuDepartment of Biologic and Materials Sciences, University of MichiganAnn Arbor, MI, United States.
Jan C-C HuDepartment of Biologic and Materials Sciences, University of MichiganAnn Arbor, MI, United States.
James P SimmerDepartment of Biologic and Materials Sciences, University of MichiganAnn Arbor, MI, United States.
Yong-Hee P ChunDepartment of Periodontics, School of Dentistry, University of Texas Health Science Center at San AntonioSan Antonio, TX, United States.
University of Michigan–Ann Arbor · USThe University of Texas Health Science Center at San Antonio · US

Funding

Institute for Integration of Medicine & Science: A Partnership to Improve HealthUL1TR001120 · NCATS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI CLARK, ROBERT A, HARGREAVES, KENNETH M · 2013 to 2017
$16.5M
Institutional Research Training GrantT32DE014318 · NIDCR · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Kenneth M Hargreaves · 2002 to 2026
$12.1M
Proteomics and Genetics of Enamel and DentinR01DE015846 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI HU, JAN CHING CHUN · 2004 to 2019
$5.7M
Enamel with overexpressed ameloblastinR01DE026769 · NIDCR · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Yong-Hee Patricia Chun · 2017 to 2026
$3.3M
Role of ameloblastin for ameloblasts and enamel formationK08DE022800 · NIDCR · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI CHUN, YONG-HEE PATRICIA · 2012 to 2016
$645k
Institute for Integration of Medicine & Science: A Partnership to Improve HealthTL1TR001119 · NCATS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI CLARK, ROBERT A, DOUGHERTY, DONALD M · 2013 to 2017
$640k
Ameloblastin concentration on enamel formationR21DE025758 · NIDCR · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI CHUN, YONG-HEE PATRICIA · 2016 to 2017
$431k
Alternative splicing of ameloblastin in enamel formationR21DE030603 · NIDCR · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI CHUN, YONG-HEE PATRICIA · 2021 to 2022
$426k
NCATS NIH HHS TL1 TR001119NCATS NIH HHS UL1 TR001120NIDCR NIH HHS K08 DE022800NIDCR NIH HHS R01 DE015846NIDCR NIH HHS R01 DE026769NIDCR NIH HHS R21 DE025758NIDCR NIH HHS R21 DE030603NIDCR NIH HHS T32 DE014318
6 · The paper itself

Abstract

Enamel formation requires consecutive stages of development to achieve its characteristic extreme mineral hardness. Mineralization depends on the initial presence then removal of degraded enamel proteins from the matrix via endocytosis. The ameloblast membrane resides at the interface between matrix and cell. Enamel formation is controlled by ameloblasts that produce enamel in stages to build the enamel layer (secretory stage) and to reach final mineralization (maturation stage). Each stage has specific functional requirements for the ameloblasts. Ameloblasts adopt different cell morphologies during each stage. Protein trafficking including the secretion and endocytosis of enamel proteins is a fundamental task in ameloblasts. The sites of internalization of enamel proteins on the ameloblast membrane are specific for every stage. In this review, an overview of endocytosis and trafficking of vesicles in ameloblasts is presented. The pathways for internalization and routing of vesicles are described. Endocytosis is proposed as a mechanism to remove debris of degraded enamel protein and to obtain feedback from the matrix on the status of the maturing enamel.

Indexed as

amelogenesisclathrinendocytic traffickingendocytosispinocytosisRab proteins

Identifiers

PMID28824442
PMCPMC5534449
OpenAlexW2741658234

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.