Evidence map›Paper›PMID 19320718›Full record

ArticleEuropean journal of oral sciences2009

Transforming growth factor-beta1 expression is up-regulated in maturation-stage enamel organ and may induce ameloblast apoptosis.

Masahiro Tsuchiya, Ramaswamy Sharma, Coralee E Tye, Toshihiro Sugiyama, John D Bartlett

Open access · greenAbstract read
In one paragraph

Article in European journal of oral sciences, 2009. 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
1.5field-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

19 citing papers in PubMed, 37 citations in OpenAlex.

  1. Review
  2. Roles of calcium in ameloblasts during tooth development: A scoping review.Journal of Taibah University Medical Sciences · 2025
    Review
  3. Review
  4. Article
  5. Role of Cell Death in Cellular Processes During Odontogenesis.Frontiers in cell and developmental biology · 2021
    Review
  6. Calcium Sets the Clock in Ameloblasts.Frontiers in physiology · 2020
    Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Apoptotic signaling in mouse odontogenesis.Omics : a journal of integrative 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

5 authors at 3 institutions in 2 countries.

Masahiro TsuchiyaDepartment of Cytokine Biology, Forsyth Institute, Harvard School of Dental Medicine, Boston, MA 02115, USA.
Ramaswamy Sharma
Coralee E Tye
Toshihiro Sugiyama
John D Bartlett
Harvard University Press · USAkita University · JPTohoku University · JP

Funding

Enamelysin Processing Mechanisms in AmelogenesisR01DE016276 · NIDCR · OHIO STATE UNIVERSITY · PI BARTLETT, JOHN D · 2006 to 2014
$4.4M
Enamelysin Processing Mechanisms in AmelogenesisR56DE016276 · NIDCR · ADA FORSYTH INSTITUTE, INC. · PI BARTLETT, JOHN D · 2011 to 2011
$498k
NIDCR NIH HHS DE 016276NIDCR NIH HHS R01 DE016276NIDCR NIH HHS R56 DE016276
6 · The paper itself

Abstract

Transforming growth factor-beta1 (TGF-beta1) regulates a variety of cellular responses that are dependent on the developmental stage and on the origins of the cell or the tissue. In mature tissues, and especially in tissues of epithelial origin, TGF-beta1 is generally considered to be a growth inhibitor that may also promote apoptosis. The ameloblast cells of the enamel organ epithelium are adjacent to and responsible for the developing enamel layer on unerupted teeth. Once the enamel layer reaches its full thickness, the tall columnar secretory-stage ameloblasts shorten, and a portion of these maturation-stage ameloblasts become apoptotic. Here we investigate whether TGF-beta1 plays a role in apoptosis of the maturation-stage ameloblasts. We demonstrate in vitro that ameloblast lineage cells are highly susceptible to TGF-beta1-mediated growth arrest and are prone to TGF-beta1-mediated cell death/apoptosis. We also demonstrate in vivo that TGF-beta1 is expressed in the maturation-stage enamel organ at significantly higher levels than in the earlier secretory-stage enamel organ. This increased expression of TGF-beta1 correlates with an increase in expression of the enamel organ immediate-early stress-response gene and with a decrease in the anti-apoptotic Bcl2 : Bax expression ratio. We conclude that TGF-beta1 may play an important role in ameloblast apoptosis during the maturation stage of enamel development.

Indexed as

AmeloblastsAnimalsApoptosisbcl-2-Associated X ProteinCell DifferentiationCells, CulturedDental EnamelDose-Response Relationship, DrugEnamel OrganGene Expression ProfilingImmediate-Early ProteinsIncisorMiceOdontogenesisProto-Oncogene ProteinsProto-Oncogene Proteins c-bcl-2bcl-2-Associated X ProteinBcl2 protein, mouseImmediate-Early ProteinsProto-Oncogene ProteinsProto-Oncogene Proteins c-bcl-2RNATransforming Growth Factor beta1

Identifiers

PMID19320718
PMCPMC2711557
OpenAlexW2020702809

What OpenQuestion holds

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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.