Evidence map›Paper›PMID 25897083›Full record

ArticleThe Journal of cell biology2015

Cell motion predicts human epidermal stemness.

Daisuke Nanba, Fujio Toki, Sota Tate, Matome Imai, Natsuki Matsushita, Ken Shiraishi, Koji Sayama, Hiroshi Toki, Shigeki Higashiyama, Yann Barrandon

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
4.8field-weighted citation impact, top 5% 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

23 citing papers in PubMed, 45 citations in OpenAlex.

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  6. Principles and mechanisms of asymmetric cell division.Development (Cambridge, England) · 2020
    Review
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  20. Tuning Collective Cell Migration by Cell-Cell Junction Regulation.Cold Spring Harbor perspectives in biology · 2017
    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

10 authors at 3 institutions in 2 countries.

Daisuke NanbaDivision of Cell Growth and Tumor Regulation, Proteo-Science Center; Department of Biochemistry and Molecular Genetics and Department of Dermatology, Graduate School of Medicine; and Translational Research Center, Ehime University Hospital, Ehime University, Toon, Ehime 791-0295, Japan Division of Cell Growth and Tumor Regulation, Proteo-Science Center; Department of Biochemistry and Molecular Genetics and Department of Dermatology, Graduate School of Medicine; and Translational Research Center, Ehime University Hospital, Ehime University, Toon, Ehime 791-0295, Japan nanba.daisuke.mk@ehime-u.ac.jp yann.barrandon@epfl.ch.
Fujio TokiDivision of Cell Growth and Tumor Regulation, Proteo-Science Center; Department of Biochemistry and Molecular Genetics and Department of Dermatology, Graduate School of Medicine; and Translational Research Center, Ehime University Hospital, Ehime University, Toon, Ehime 791-0295, Japan.
Sota TateDivision of Cell Growth and Tumor Regulation, Proteo-Science Center; Department of Biochemistry and Molecular Genetics and Department of Dermatology, Graduate School of Medicine; and Translational Research Center, Ehime University Hospital, Ehime University, Toon, Ehime 791-0295, Japan.
Matome ImaiDivision of Cell Growth and Tumor Regulation, Proteo-Science Center; Department of Biochemistry and Molecular Genetics and Department of Dermatology, Graduate School of Medicine; and Translational Research Center, Ehime University Hospital, Ehime University, Toon, Ehime 791-0295, Japan.
Natsuki MatsushitaDivision of Cell Growth and Tumor Regulation, Proteo-Science Center; Department of Biochemistry and Molecular Genetics and Department of Dermatology, Graduate School of Medicine; and Translational Research Center, Ehime University Hospital, Ehime University, Toon, Ehime 791-0295, Japan.
Ken ShiraishiDivision of Cell Growth and Tumor Regulation, Proteo-Science Center; Department of Biochemistry and Molecular Genetics and Department of Dermatology, Graduate School of Medicine; and Translational Research Center, Ehime University Hospital, Ehime University, Toon, Ehime 791-0295, Japan.
Koji SayamaDivision of Cell Growth and Tumor Regulation, Proteo-Science Center; Department of Biochemistry and Molecular Genetics and Department of Dermatology, Graduate School of Medicine; and Translational Research Center, Ehime University Hospital, Ehime University, Toon, Ehime 791-0295, Japan.
Hiroshi TokiResearch Center for Nuclear Physics, Osaka University, Ibaraki, Osaka 567-0047, Japan.
Shigeki HigashiyamaDivision of Cell Growth and Tumor Regulation, Proteo-Science Center; Department of Biochemistry and Molecular Genetics and Department of Dermatology, Graduate School of Medicine; and Translational Research Center, Ehime University Hospital, Ehime University, Toon, Ehime 791-0295, Japan Division of Cell Growth and Tumor Regulation, Proteo-Science Center; Department of Biochemistry and Molecular Genetics and Department of Dermatology, Graduate School of Medicine; and Translational Research Center, Ehime University Hospital, Ehime University, Toon, Ehime 791-0295, Japan.
Yann BarrandonLaboratory of Stem Cell Dynamics, École Polytechnique Fédérale de Lausanne, CH-1015 Lausanne, Switzerland Department of Experimental Surgery, Centre Hospitalier Universitaire Vaudois, CH-1011 Lausanne, Switzerland nanba.daisuke.mk@ehime-u.ac.jp yann.barrandon@epfl.ch.
Ehime University Hospital · JPÉcole Polytechnique Fédérale de Lausanne · CHOsaka University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Image-based identification of cultured stem cells and noninvasive evaluation of their proliferative capacity advance cell therapy and stem cell research. Here we demonstrate that human keratinocyte stem cells can be identified in situ by analyzing cell motion during their cultivation. Modeling experiments suggested that the clonal type of cultured human clonogenic keratinocytes can be efficiently determined by analysis of early cell movement. Image analysis experiments demonstrated that keratinocyte stem cells indeed display a unique rotational movement that can be identified as early as the two-cell stage colony. We also demonstrate that α6 integrin is required for both rotational and collective cell motion. Our experiments provide, for the first time, strong evidence that cell motion and epidermal stemness are linked. We conclude that early identification of human keratinocyte stem cells by image analysis of cell movement is a valid parameter for quality control of cultured keratinocytes for transplantation.

Indexed as

Epidermal CellsBlotting, WesternCell DifferentiationCell MovementCell ProliferationCells, CulturedCell SeparationComputer SimulationEpidermisFlow CytometryFluorescent Antibody TechniqueHumansIntegrin alpha6KeratinocytesReal-Time Polymerase Chain ReactionReverse Transcriptase Polymerase Chain ReactionIntegrin alpha6RNA, Messenger

Identifiers

PMID25897083
PMCPMC4411274
OpenAlexW2136009951

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.