Evidence map›Paper›PMID 23489896›Full record

ArticleEuropean journal of oral sciences2013

Role of the NH2 -terminal fragment of dentin sialophosphoprotein in dentinogenesis.

Monica P Gibson, Qilin Liu, Qinglin Zhu, Yongbo Lu, Priyam Jani, Xiaofang Wang, Ying Liu, Michael L Paine, Malcolm L Snead, Jian Q Feng and 1 more

Open access · greenAbstract read
In one paragraph

Article in European journal of oral sciences, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.3field-weighted citation impact, top 14% 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

17 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Haploinsufficiency ofFrontiers in physiology · 2020
    Article
  7. Article
  8. Review
  9. Article
  10. Effects of Btbd7 knockdown on the proliferation of human dental pulp cells and expression of Dspp.International journal of clinical and experimental pathology · 2018
    Article
  11. Review
  12. Article
  13. Article
  14. Dentin Matrix Proteins in Bone Tissue Engineering.Advances in experimental medicine and biology · 2015
    Review
  15. Overexpressing the NHJournal of oral biosciences · 2014
    Article
  16. Article
  17. Accelerated enamel mineralization in Dspp mutant mice.Matrix biology : journal of the International Society for Matrix Biology
    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

11 authors at 1 institution in 1 country.

Monica P GibsonTexas A&M Health Science Center Baylor College of Dentistry, Dallas, TX 75246, USA.
Qilin Liu
Qinglin Zhu
Yongbo Lu
Priyam Jani
Xiaofang Wang
Ying Liu
Michael L Paine
Malcolm L Snead
Jian Q Feng
Chunlin Qin
University of Southern California · US

Funding

Studies of the Roles of DMP1 and DSPP in Osteogenesis and DentinogenesisR01DE005092 · NIDCR · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI QIN, CHUNLIN · 1985 to 2012
$4.4M
STUDIES OF PROTEINS INVOLVED IN DENTINOGENESISR37DE005092 · NIDCR · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI BUTLER, WILLIAM T · 1987 to 1996
–
NIDCR NIH HHS DE005092NIDCR NIH HHS DE015209NIDCR NIH HHS R01 DE005092
6 · The paper itself

Abstract

Dentin sialophosphoprotein (DSPP) is a large precursor protein that is proteolytically processed into a NH2 -terminal fragment [composed of dentin sialoprotein (DSP) and a proteoglycan form (DSP-PG)] and a COOH-terminal fragment [dentin phosphoprotein (DPP)]. In vitro studies indicate that DPP is a strong initiator and regulator of hydroxyapatite crystal formation and growth, but the role(s) of the NH2 -terminal fragment of DSPP (i.e., DSP and DSP-PG) in dentinogenesis remain unclear. This study focuses on the function of the NH2 -terminal fragment of DSPP in dentinogenesis. Here, transgenic (Tg) mouse lines expressing the NH2 -terminal fragment of DSPP driven by a 3.6-kb type I collagen promoter (Col 1a1) were generated and cross-bred with Dspp null mice to obtain mice that express the transgene but lack the endogenous Dspp (Dspp KO/DSP Tg). We found that dentin from the Dspp KO/DSP Tg mice was much thinner, more poorly mineralized, and remarkably disorganized compared with dentin from the Dspp KO mice. The fact that Dspp KO/DSP Tg mice exhibited more severe dentin defects than did the Dspp null mice indicates that the NH2 -terminal fragment of DSPP may inhibit dentin mineralization or may serve as an antagonist against the accelerating action of DPP and serve to prevent predentin from being mineralized too rapidly during dentinogenesis.

Indexed as

AnimalsDentinDentinogenesisDentin SialophosphoproteinExtracellular Matrix ProteinsImmunohistochemistryMiceMice, KnockoutMicroscopy, Electron, ScanningPhosphoproteinsReal-Time Polymerase Chain ReactionRNA, MessengerSialoglycoproteinsTooth CalcificationX-Ray MicrotomographyDentin SialophosphoproteinExtracellular Matrix ProteinsPhosphoproteinsRNA, MessengerSialoglycoproteins

Identifiers

PMID23489896
PMCPMC3602929
OpenAlexW1992247331

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.