Evidence map›Paper›PMID 42399254›Full record

ArticleNature communications2026

Ectomesenchyme contributes to epidermal stem cell formation through mesenchymal-to-epithelial transition.

Asaka Miura, Yuki Kobayashi, Yoshikazu Hirose, Tomoyuki Azuma, Takashi Shimbo, Yuya Ouchi, Tomomi Kitayama, Ryoma Yamamoto, Eiichi Takaki, Sho Yamazaki and 7 more

Abstract read
In one paragraph

Article in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

17 authors.

Asaka Miura *Department of Stem Cell Therapy Science, Graduate School of Medicine, The University of Osaka, Suita, Osaka, Japan.
Yuki Kobayashi *StemRIM Inc., Ibaraki, Osaka, Japan.
Yoshikazu HiroseDepartment of Stem Cell Therapy Science, Graduate School of Medicine, The University of Osaka, Suita, Osaka, Japan.
Tomoyuki AzumaStemRIM Inc., Ibaraki, Osaka, Japan.
Takashi ShimboDepartment of Stem Cell Therapy Science, Graduate School of Medicine, The University of Osaka, Suita, Osaka, Japan.ORCID http://orcid.org/0000-0002-0056-8814
Yuya OuchiStemRIM Inc., Ibaraki, Osaka, Japan.
Tomomi KitayamaStemRIM Inc., Ibaraki, Osaka, Japan.
Ryoma YamamotoStemRIM Inc., Ibaraki, Osaka, Japan.
Eiichi TakakiStemRIM Inc., Ibaraki, Osaka, Japan.
Sho YamazakiStemRIM Inc., Ibaraki, Osaka, Japan.
Machika KawamuraStemRIM Inc., Ibaraki, Osaka, Japan.
Aino SasabuchiDepartment of Molecular Craniofacial Embryology and Oral Histology, Graduate School of Medical and Dental Sciences, Institute of Science Tokyo, Bunkyo-ku, Tokyo, Japan.ORCID http://orcid.org/0009-0001-7994-1350
Kotaro SagaDepartment of Stem Cell Therapy Science, Graduate School of Medicine, The University of Osaka, Suita, Osaka, Japan.
Sachiko IsekiDepartment of Molecular Craniofacial Embryology and Oral Histology, Graduate School of Medical and Dental Sciences, Institute of Science Tokyo, Bunkyo-ku, Tokyo, Japan.ORCID http://orcid.org/0000-0001-8448-9410
Yasufumi KanedaDivision of Gene Therapy Science, Graduate School of Medicine, The University of Osaka, Suita, Osaka, Japan.
Manabu FujimotoDepartment of Dermatology, Graduate School of Medicine, The University of Osaka, Suita, Osaka, Japan.
Katsuto TamaiDepartment of Stem Cell Therapy Science, Graduate School of Medicine, The University of Osaka, Suita, Osaka, Japan. tamai@sts.med.osaka-u.ac.jp.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cutaneous development is initiated by crosstalk between non-neural ectodermal epithelium and underlying mesenchymal cells. Recent studies have shown that some mesenchymal cells contribute to keratinocyte regeneration in injured skin. However, whether mesenchymal cells contribute to keratinocyte formation in physiologically normal skin remains unclear. Here we show, using lineage tracing, single-cell transcriptome and epigenome analyses of mouse skin, that the interfollicular epidermis consists largely of mesenchymal-lineage cells. Further lineage-tracing and live-imaging analysis of mouse embryos indicate that these mesenchymal-lineage epidermal progenitor cells arise from ectomesenchyme and contribute to the surface ectoderm through a mesenchymal-to-epithelial transition-like process between embryonic days 8.5 and 9.5. We also establish human induced pluripotent stem cell-derived ectomesenchyme and demonstrate that it generates p63-expressing keratinocytes. These data reveal a previously unappreciated contribution of ectomesenchyme to cutaneous development and provide insight into skin diseases involving epidermal mosaicism.

Indexed as

EctodermEpidermal CellsEpithelial-Mesenchymal TransitionMesodermStem CellsAnimalsCell DifferentiationCell LineageEpidermisHumansInduced Pluripotent Stem CellsKeratinocytesMesenchymal Stem CellsMiceSkinTrans-ActivatorsTrans-ActivatorsTrp63 protein, mouse

Identifiers

PMID42399254
PMCPMC13469143

What Socratic 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 Socratic graph.