Evidence map›Paper›PMID 23813243›Full record

ArticleIn vitro cellular & developmental biology. Animal2013

Immortalized mouse dental papilla mesenchymal cells preserve odontoblastic phenotype and respond to bone morphogenetic protein 2.

Feng Wang, Li-An Wu, Wentong Li, Yuan Yang, Feng Guo, Qingping Gao, Hui-Hsiu Chuang, Lisa Shoff, Wei Wang, Shuo Chen

Open access · hybridAbstract read
In one paragraph

Article in In vitro cellular & developmental biology. Animal, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

10 citing papers in PubMed, 22 citations in OpenAlex.

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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

10 authors at 3 institutions in 2 countries.

Feng WangDepartment of Developmental Dentistry, Dental School, The University of Texas Health Science Center at San Antonio, 7703 Floyd Curl Drive, San Antonio, TX, 78229-3900, USA.
Li-An Wu
Wentong Li
Yuan Yang
Feng Guo
Qingping Gao
Hui-Hsiu Chuang
Lisa Shoff
Wei Wang
Shuo Chen
The University of Texas Health Science Center at San Antonio · USAir Force Medical University · CNFujian Medical University · CN

Funding

DSPP signaling in dentinogenesisR01DE019802 · NIDCR · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Shuo Chen · 2009 to 2026
$3.4M
Development of iPS cells to study craniometaphyseal dysplasia in humansR21DE019892 · NIDCR · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI LICHTLER, ALEXANDER C, REICHENBERGER, ERNST J · 2009 to 2010
$356k
NIDCR NIH HHS DE019892NIDCR NIH HHS R01 DE019802NIDCR NIH HHS R21 DE019892
6 · The paper itself

Abstract

Odontogenesis is the result of the reciprocal interactions between epithelial-mesenchymal cells leading to terminally differentiated odontoblasts. This process from dental papilla mesenchymal cells to odontoblasts is regulated by a complex signaling pathway. When isolated from the developing tooth germs, odontoblasts quickly lose their potential to maintain the odontoblast-specific phenotype. Therefore, generation of an odontoblast-like cell line would be a good surrogate model for studying the dental mesenchymal cell differentiation into odontoblasts and the molecular events of dentin formation. In this study, immortalized dental papilla mesenchymal cell lines were generated from the first mouse mandibular molars at postnatal day 3 using pSV40. These transformed cells were characterized by RT-PCR, immunohistochemistry, Western blot, and analyzed for alkaline phosphatase activity and mineralization nodule formation. One of these immortalized cell lines, iMDP-3, displayed a high proliferation rate, but retained the genotypic and phenotypic characteristics similar to primary cells as determined by expression of tooth-specific markers and demonstrated the ability to differentiate and form mineralized nodules. Furthermore, iMDP-3 cells had high transfection efficiency as well as were inducible and responded to BMP2 stimulation. We conclude that the establishment of the stable murine dental papilla mesenchymal cell line might be used for studying the mechanisms of dental cell differentiation and dentin formation.

Indexed as

AnimalsAntigens, Viral, TumorBone Morphogenetic Protein 2Cell DifferentiationCells, CulturedDental PapillaEpithelial CellsGene Expression Regulation, DevelopmentalHumansMesodermMiceOdontoblastsOdontogenesisToothTransfectionAntigens, Viral, TumorBMP2 protein, humanBone Morphogenetic Protein 2

Identifiers

PMID23813243
PMCPMC3779316
OpenAlexW2066440651

What OpenQuestion holds

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LicenceCC BY-NC
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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.