Evidence map›Paper›PMID 30944469›Full record

ArticleNature2019

Stem cell competition orchestrates skin homeostasis and ageing.

Nan Liu, Hiroyuki Matsumura, Tomoki Kato, Shizuko Ichinose, Aki Takada, Takeshi Namiki, Kyosuke Asakawa, Hironobu Morinaga, Yasuaki Mohri, Adèle De Arcangelis and 3 more

Abstract read
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In one paragraph

Article in Nature, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 215 papers.

0numbers the graph read from it
0cells of the map it votes in
215citing papers in PubMed
44.0field-weighted citation impact, top 1% 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

215 citing papers in PubMed, 397 citations in OpenAlex.

  1. Trial
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  8. An updated guide to hair follicle stem cell markers and changes in their expression with aging.JID innovations : skin science from molecules to population health · 2026
    Review
  9. Article
  10. Cell proliferation and differentiation during epidermis renewal.Journal of Zhejiang University. Science. B · 2026
    Review
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  12. Article
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  14. Article
  15. Article
  16. Review
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  19. Article
  20. Article

155 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 3 institutions in 2 countries.

Nan Liu *Department of Stem Cell Biology, Medical Research Institute, Tokyo Medical and Dental University, Tokyo, Japan.
Hiroyuki Matsumura *Department of Stem Cell Biology, Medical Research Institute, Tokyo Medical and Dental University, Tokyo, Japan. matsscm@tmd.ac.jp.
Tomoki KatoDepartment of Stem Cell Biology, Medical Research Institute, Tokyo Medical and Dental University, Tokyo, Japan.
Shizuko IchinoseResearch Center for Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo, Japan.
Aki TakadaDepartment of Stem Cell Biology, Medical Research Institute, Tokyo Medical and Dental University, Tokyo, Japan.
Takeshi NamikiDepartment of Dermatology, Tokyo Medical and Dental University Graduate School and Faculty of Medicine, Tokyo, Japan.
Kyosuke AsakawaDepartment of Stem Cell Biology, Medical Research Institute, Tokyo Medical and Dental University, Tokyo, Japan.
Hironobu MorinagaDepartment of Stem Cell Biology, Medical Research Institute, Tokyo Medical and Dental University, Tokyo, Japan.
Yasuaki MohriDepartment of Stem Cell Biology, Medical Research Institute, Tokyo Medical and Dental University, Tokyo, Japan.
Adèle De ArcangelisCNRS UMR7104, Inserm U1258, Institut de Génétique et de Biologie Moléculaire et Cellulaire, Development and Stem Cells Department, Université de Strasbourg, Strasbourg, France.
Elisabeth Geroges-LabouesseCNRS UMR7104, Inserm U1258, Institut de Génétique et de Biologie Moléculaire et Cellulaire, Development and Stem Cells Department, Université de Strasbourg, Strasbourg, France.
Daisuke NanbaDepartment of Stem Cell Biology, Medical Research Institute, Tokyo Medical and Dental University, Tokyo, Japan.
Emi K NishimuraDepartment of Stem Cell Biology, Medical Research Institute, Tokyo Medical and Dental University, Tokyo, Japan. nishscm@tmd.ac.jp.
Tokyo Medical and Dental University · JPInserm · FRUniversité de Strasbourg · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Stem cells underlie tissue homeostasis, but their dynamics during ageing-and the relevance of these dynamics to organ ageing-remain unknown. Here we report that the expression of the hemidesmosome component collagen XVII (COL17A1) by epidermal stem cells fluctuates physiologically through genomic/oxidative stress-induced proteolysis, and that the resulting differential expression of COL17A1 in individual stem cells generates a driving force for cell competition. In vivo clonal analysis in mice and in vitro 3D modelling show that clones that express high levels of COL17A1, which divide symmetrically, outcompete and eliminate adjacent stressed clones that express low levels of COL17A1, which divide asymmetrically. Stem cells with higher potential or quality are thus selected for homeostasis, but their eventual loss of COL17A1 limits their competition, thereby causing ageing. The resultant hemidesmosome fragility and stem cell delamination deplete adjacent melanocytes and fibroblasts to promote skin ageing. Conversely, the forced maintenance of COL17A1 rescues skin organ ageing, thereby indicating potential angles for anti-ageing therapeutic intervention.

Indexed as

HomeostasisAnimalsAtrophyAutoantigensCell DivisionCell ProliferationClone CellsCollagen Type XVIIEpidermal CellsFemaleGenomeHemidesmosomesMaleMiceMice, Inbred C57BLModels, AnimalAutoantigensCollagen Type XVIINon-Fibrillar Collagens

Identifiers

PMID30944469
OpenAlexW2932503900

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.