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Human keratinocytes have two interconvertible modes of proliferation.


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Authors

Murai, Kasumi 
Fowler, Joanna 
Simons, Benjamin D 
Nikolaidou-Neokosmidou, Varvara 

Abstract

Single stem cells, including those in human epidermis, have a remarkable ability to reconstitute tissues in vitro, but the cellular mechanisms that enable this are ill-defined. Here we used live imaging to track the outcome of thousands of divisions in clonal cultures of primary human epidermal keratinocytes. Two modes of proliferation were seen. In 'balanced' mode, similar proportions of proliferating and differentiating cells were generated, achieving the 'population asymmetry' that sustains epidermal homeostasis in vivo. In 'expanding' mode, an excess of cycling cells was produced, generating large expanding colonies. Cells in expanding mode switched their behaviour to balanced mode once local confluence was attained. However, when a confluent area was wounded in a scratch assay, cells near the scratch switched back to expanding mode until the defect was closed. We conclude that the ability of a single epidermal stem cell to reconstitute an epithelium is explained by two interconvertible modes of proliferation regulated by confluence.

Description

Keywords

Cell Cycle, Cell Differentiation, Cell Movement, Cell Proliferation, Cells, Cultured, Epidermal Growth Factor, Homeostasis, Humans, Infant, Newborn, Keratinocytes, Male, Microscopy, Video, Phenotype, Signal Transduction, Stem Cells, Time Factors, Time-Lapse Imaging, rho-Associated Kinases

Journal Title

Nat Cell Biol

Conference Name

Journal ISSN

1465-7392
1476-4679

Volume Title

18

Publisher

Springer Science and Business Media LLC
Sponsorship
Medical Research Council (MC_UU_12022/3)
Wellcome Trust (098357/Z/12/Z)
Cancer Research UK (C609/A17257)
MRC (unknown)
Wellcome Trust (090334/Z/09/Z)
Wellcome Trust (092096/Z/10/Z)
Wellcome Trust (097922/Z/11/B)
Medical Research Council (MC_UU_12022/5)
The initial association of holoclone and paraclone type behaviour in clonal cultures of NFSK with stem and balanced progenitor dynamics was due to BDS working in collaboration with PHJ, VN-N, David Doupé and Allon Klein, based on the quantitative analysis of published and unpublished colony size distributions6 . We thank Gözde Akdeniz & David Doupé for experimental work that led up to the project that was analysed by Allon Klein and Genneth Zhang, Patrick Lombard at the Wellcome TrustMedical Research Council Cambridge Stem Cell Institute for Bioinformatics analysis and Esther Choolun for technical assistance. We acknowledge the support of the Wellcome Trust, Cambridge Cancer Centre, Medical Research Council, the NC3Rs (National Centre for the Replacement, Refinement and Reduction of Animals in Research) and Cancer Research UK (Programme grant C609/A17257).