Evidence map›Paper›PMID 41296682›Full record

ArticleStem cells (Dayton, Ohio)2026

Stem cell specification and niche formation in developing incisor require actomyosin forces.

Yasmin Mohtadi Hamadani, Laura Evers, Satu-Marja Myllymäki, Emma Juuri, Maria Jussila, Paul Gueguen, Mina Mina, Irma Thesleff, Anamaria Balic

Abstract read
In one paragraph

Article in Stem cells (Dayton, Ohio), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

9 authors.

Yasmin Mohtadi HamadaniInstitute of Oral Biology, Centre for Dental Medicine, University of Zurich, Zurich 8032, Switzerland.
Laura EversInstitute of Oral Biology, Centre for Dental Medicine, University of Zurich, Zurich 8032, Switzerland.
Satu-Marja MyllymäkiStem Cells and Metabolism Research Program, Faculty of Medicine, University of Helsinki, Helsinki 00014, Finland.
Emma JuuriCleft Palate and Craniofacial Center, Department of Plastic Surgery, Helsinki University Central Hospital, Helsinki 00029, Finland.
Maria JussilaInstitute of Biotechnology, HiLIFE, University of Helsinki, Helsinki 00790, Finland.
Paul GueguenFunctional Genomics Center Zurich, ETH Zurich and University of Zurich, Zurich 8057, Switzerland.
Mina MinaDepartment of Pediatric Dentistry, University of Connecticut Health Center, Farmington, CT 06030, United States.
Irma ThesleffInstitute of Biotechnology, HiLIFE, University of Helsinki, Helsinki 00790, Finland.
Anamaria BalicInstitute of Oral Biology, Centre for Dental Medicine, University of Zurich, Zurich 8032, Switzerland.ORCID 0000-0001-6796-1197

Funding

Dental Association 357-24Jane and Aatos Erkko FoundationSwiss National Science Foundation 310030_215594
6 · The paper itself

Abstract

backgroundThe precise timing of stem cell specification and niche formation during murine incisor development is poorly understood, and it is unclear whether these processes occur simultaneously or in a sequential manner. Functional dental epithelial stem cells are marked by the expression of Sox2, a transcription factor that is broadly expressed in the dental epithelium at the dentition onset and restricted to stem cells in fully developed incisor.

methodsUsing genetic lineage tracing in Sox2CreERT2/+; R26RmT/mG and Sox2CreERT2/+; R26RtdT/+ embryos along with a single-cell RNA sequencing at different stages of incisor development, we investigated the timing of the stem cell specification and its temporal relationship with niche formation.

resultsOur results reveal the presence of a Sox2-expressing stem cell-like population prior to formation of the functional niche. These cells localize to the leading edge of the advancing incisor epithelium where they are maintained in an undifferentiated state. Our data demonstrate presence of actomyosin network and a generation of a contractile tension, which helps confine Sox2+ stem cells to the leading edge.

conclusionThis mechanical confinement likely plays an important role in maintaining their stemness until the niche is functionally and structurally established. Partial or complete disruption of the actomyosin network disables the clustering of Sox2-expressing cells, potentially triggering their premature differentiation, and ultimately leads to impaired formation of the functional stem cell niche and abnormal growth of the incisor.

Indexed as

ActomyosinIncisorStem Cell NicheStem CellsAnimalsCell DifferentiationMiceSOXB1 Transcription FactorsActomyosinSox2 protein, mouseSOXB1 Transcription Factorsactomyosin forcecontinuously growing incisorsingle-cell RNA sequencingSox2stem cell niche formation

Identifiers

PMID41296682
PMCPMC12855154

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.