Evidence map›Paper›PMID 23362283›Full record

ArticleThe Journal of biological chemistry2013

Dentin phosphophoryn activates Smad protein signaling through Ca2+-calmodulin-dependent protein kinase II in undifferentiated mesenchymal cells.

Asha Eapen, Roma Kulkarni, Sriram Ravindran, Amsaveni Ramachandran, Premanand Sundivakkam, Chinnaswammy Tiruppathi, Anne George

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

20 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. CaFrontiers in cell and developmental biology · 2025
    Article
  5. Article
  6. Article
  7. CaMKII inhibition due to TRIC-B loss-of-function dysregulates SMAD signaling in osteogenesis imperfecta.Matrix biology : journal of the International Society for Matrix Biology · 2023
    Article
  8. Article
  9. New Insights into TRP Ion Channels in Stem Cells.International journal of molecular sciences · 2022
    Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Dentin Matrix Proteins in Bone Tissue Engineering.Advances in experimental medicine and biology · 2015
    Review
  18. Article
  19. Multifunctional ECM proteins in bone and teeth.Experimental cell research · 2014
    Review
  20. 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

7 authors at 1 institution in 1 country.

Asha EapenDepartment of Oral Biology, University of Illinois, Chicago, Illinois 60612.
Roma KulkarniDepartment of Oral Biology, University of Illinois, Chicago, Illinois 60612.
Sriram RavindranDepartment of Oral Biology, University of Illinois, Chicago, Illinois 60612.
Amsaveni RamachandranDepartment of Oral Biology, University of Illinois, Chicago, Illinois 60612.
Premanand SundivakkamDepartment of Pharmacology, University of Illinois, Chicago, Illinois 60612.
Chinnaswammy TiruppathiDepartment of Pharmacology, University of Illinois, Chicago, Illinois 60612.
Anne GeorgeDepartment of Oral Biology, University of Illinois, Chicago, Illinois 60612. Electronic address: anneg@uic.edu.
University of Illinois Chicago · US

Funding

Trpm2 Regulation of Phagocyte Bactericidal Activity and Resolution of Lung InjuryP01HL077806 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI MALIK, ASRAR B. · 2005 to 2019
$27.0M
Intracellular and Extracellular function of dentin phosphophorynR01DE019633 · NIDCR · UNIVERSITY OF ILLINOIS AT CHICAGO · PI GEORGE, ANNE · 2010 to 2013
$1.5M
NHLBI NIH HHS P01 HL077806NIDCR NIH HHS DE 19633NIDCR NIH HHS R01 DE019633
6 · The paper itself

Abstract

Dentin phosphophoryn (DPP) is a major noncollagenous protein in the dentin matrix. In this study, we demonstrate that pluripotent stem cells such as C3H10T1/2 and human bone marrow cells can be committed to the osteogenic lineage by DPP. Treatment with DPP can stimulate the release of intracellular Ca(2+). This calcium flux triggered the activation of Ca(2+)-calmodulin-dependent protein kinase II (CaMKII). Activated CaMKII induced the phosphorylation of Smad1 and promoted nuclear translocation of p-Smad1. Inhibition of store Ca(2+) depletion by 1,2-bis(2-aminophenoxy)ethane-N,N,N',N'-tetraacetic acid tetrakis(acetoxymethyl ester) or down-regulation of CaMKII by KN-62, a selective cell-permeable pharmacological inhibitor or a dominant negative plasmid of CaMKII, blocked DPP-mediated Smad1 phosphorylation. Activation of Smad1 resulted in the expression of osteogenic markers such as Runx2, Osterix, DMP1, Bone sialoprotein, Osteocalcin, NFATc1, and Schnurri-2, which have been implicated in osteoblast differentiation. These findings suggest that DPP is capable of triggering commitment of pluripotent stem cells to the osteogenic lineage.

Indexed as

Calcium SignalingCell Differentiation1-(5-Isoquinolinesulfonyl)-2-MethylpiperazineAnimalsAntigens, DifferentiationCalcium-Calmodulin-Dependent Protein Kinase Type 2CattleCell NucleusCells, CulturedDentin SialophosphoproteinDNA-Binding ProteinsEnzyme ActivationExtracellular Matrix ProteinsHumansMesenchymal Stem CellsMice1-(5-Isoquinolinesulfonyl)-2-MethylpiperazineAntigens, DifferentiationCalcium-Calmodulin-Dependent Protein Kinase Type 2Dentin SialophosphoproteinDNA-Binding ProteinsExtracellular Matrix ProteinsHIVEP2 protein, humanKN 62NFATC1 protein, humanNFATC Transcription FactorsPhosphoproteinsSialoglycoproteinsSmad1 ProteinSMAD1 protein, humanSmad Proteins, Receptor-RegulatedTranscription Factors

Identifiers

PMID23362283
PMCPMC3605677
OpenAlexW2008696955

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.