Cell motion predicts human epidermal stemness
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Updated: Apr 14, 2026

Assessing Neural Stem Cell Motility Using an Agarose Gel-based Microfluidic Device
Published on: February 11, 2008
Daisuke Nanba1, Fujio Toki2, Sota Tate2
1Division 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.
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.
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