Evidence map›Paper›PMID 26160988›Full record

ArticleActa histochemica et cytochemica2015

Hertwig's Epithelial Root Sheath Fate during Initial Cellular Cementogenesis in Rat Molars.

Tsuneyuki Yamamoto, Tamaki Yamada, Tomomaya Yamamoto, Tomoka Hasegawa, Hiromi Hongo, Kimimitsu Oda, Norio Amizuka

Abstract read
In one paragraph

Article in Acta histochemica et cytochemica, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
  2. Review
  3. Expressions of cytokeratin 14 and proliferating cell nuclear antigen in the Hertwig's epithelial root sheath of a Vps4b knockout mouse.Hua xi kou qiang yi xue za zhi = Huaxi kouqiang yixue zazhi = West China journal of stomatology · 2021
    Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Multiple essential MT1-MMP functions in tooth root formation, dentinogenesis, and tooth eruption.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

7 authors.

Tsuneyuki YamamotoDepartment of Developmental Biology of Hard Tissue, Hokkaido University Graduate School of Dental Medicine , Sapporo, Japan.
Tamaki YamadaDepartment of Developmental Biology of Hard Tissue, Hokkaido University Graduate School of Dental Medicine , Sapporo, Japan.
Tomomaya YamamotoDepartment of Developmental Biology of Hard Tissue, Hokkaido University Graduate School of Dental Medicine , Sapporo, Japan.
Tomoka HasegawaDepartment of Developmental Biology of Hard Tissue, Hokkaido University Graduate School of Dental Medicine , Sapporo, Japan.
Hiromi HongoDepartment of Developmental Biology of Hard Tissue, Hokkaido University Graduate School of Dental Medicine , Sapporo, Japan.
Kimimitsu OdaDivision of Biochemistry, Niigata University Graduate School of Medical and Dental Sciences , Niigata, Japan.
Norio AmizukaDepartment of Developmental Biology of Hard Tissue, Hokkaido University Graduate School of Dental Medicine , Sapporo, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To elucidate the fate of the epithelial root sheath during initial cellular cementogenesis, we examined developing maxillary first molars of rats by immunohistochemistry for keratin, vimentin, and tissue non-specific alkaline phosphatase (TNALP) and by TdT-mediated dUTP nick end labeling (TUNEL). The advancing root end was divided into three sections, which follow three distinct stages of initial cellular cementogenesis: section 1, where the epithelial sheath is intact; section 2, where the epithelial sheath becomes fragmented; and section 3, where initial cellular cementogenesis begins. After fragmentation of the epithelial sheath, many keratin-positive epithelial sheath cells were embedded in the rapidly growing cellular cementum. A few unembedded epithelial cells located on the cementum surface. Dental follicle cells, precementoblasts, and cementoblasts showed immunoreactivity for vimentin and TNALP. In all three sections, there were virtually no cells possessing double immunoreactivity for vimentin-keratin or TNALP-keratin and only embedded epithelial cells showed TUNEL reactivity. Taken together, these findings suggest that: (1) epithelial sheath cells divide into two groups; one group is embedded in the cementum and thereafter dies by apoptosis, and the other survives on the cementum surface as epithelial cell rests of Malassez; and (2) epithelial sheath cells do not undergo epithelial-mesenchymal transition during initial cellular cementogenesis.

Indexed as

cellular cementumcementoblastsepithelial-mesenchymal transitionHertwig’s epithelial root sheathrat molars

Identifiers

PMID26160988
PMCPMC4491499

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.