Evidence map›Paper›PMID 25081036›Full record

ArticleMolecules and cells2014

Establishment of Hertwig's epithelial root sheath/epithelial rests of Malassez cell line from human periodontium.

Hyun Nam, Ji-Hye Kim, Jae-Won Kim, Byoung-Moo Seo, Joo-Cheol Park, Jung-Wook Kim, Gene Lee

Abstract read
In one paragraph

Article in Molecules and cells, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–field-weighted citation impact
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

14 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Molecules and cells · 2016
    Article
  13. Human odontogenic epithelial cells derived from epithelial rests of Malassez possess stem cell properties.Laboratory investigation; a journal of technical methods and pathology · 2016
    Article
  14. Odontogenic epithelial stem cells: hidden sources.Laboratory investigation; a journal of technical methods and pathology · 2015
    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

7 authors.

Hyun NamLaboratory of Molecular Genetics, Dental Research Institute, School of Dentistry, Seoul National University, Seoul 110-749, Korea ; Present address: Samsung Medical Center, School of Medicine, Sungkyunkwan University, Seoul 135-710, Korea.
Ji-Hye KimLaboratory of Molecular Genetics, Dental Research Institute, School of Dentistry, Seoul National University, Seoul 110-749, Korea.
Jae-Won KimLaboratory of Molecular Genetics, Dental Research Institute, School of Dentistry, Seoul National University, Seoul 110-749, Korea.
Byoung-Moo SeoDepartment of Oral and Maxillofacial Surgery, Seoul National University, Seoul 110-749, Korea.
Joo-Cheol ParkDepartment of Oral Histology-Developmental Biology, Seoul National University, Seoul 110-749, Korea.
Jung-Wook KimDepartment of Pediatric Dentistry, Seoul National University, Seoul 110-749, Korea.
Gene LeeLaboratory of Molecular Genetics, Dental Research Institute, School of Dentistry, Seoul National University, Seoul 110-749, Korea.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human Hertwig's epithelial root sheath/epithelial rests of Malassez (HERS/ERM) cells are epithelial remnants of teeth residing in the periodontium. Although the functional roles of HERS/ERM cells have yet to be elucidated, they are a unique epithelial cell population in adult teeth and are reported to have stem cell characteristics. Therefore, HERS/ERM cells might play a role as an epithelial component for the repair or regeneration of dental hard tissues; however, they are very rare population in periodontium and the primary isolation of them is considered to be difficult. To overcome these problems, we immortalized primary HERS/ERM cells isolated from human periodontium using SV40 large T antigen (SV40 LT) and performed a characterization of the immortalized cell line. Primary HERS/ERM cells could not be maintained for more than 6 passages; however, immortalized HERS/ERM cells were maintained for more than 20 passages. There were no differences in the morphological and immunophenotypic characteristics of HERS/ERM cells and immortalized HERS/ERM cells. The expression of epithelial stem cell and embryonic stem cell markers was maintained in immortalized HERS/ERM cells. Moreover, immortalized HERS/ERM cells could acquire mesenchymal phenotypes through the epithelial-mesenchymal transition via TGF-β1. In conclusion, we established an immortalized human HERS/ERM cell line with SV40 LT and expect this cell line to contribute to the understanding of the functional roles of HERS/ERM cells and the tissue engineering of teeth.

Indexed as

Guided Tissue Regeneration, PeriodontalAdultAdult Stem CellsAntigens, Polyomavirus TransformingBiomarkersCell Line, TransformedCell SeparationEpithelial CellsEpithelial-Mesenchymal TransitionHumansPeriodontiumPhenotypePrimary Cell CultureTooth RootTransforming Growth Factor beta1Antigens, Polyomavirus TransformingBiomarkersTransforming Growth Factor beta1epithelial-mesenchymal transitionHertwig's epithelial root sheath/epithelial rests of Malassez cellsimmortalizationstemnessSV40 large T antigen

Identifiers

PMID25081036
PMCPMC4132309

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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.