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Cell
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License: Elsevier Non-Commercial
Data sources: UnpayWall
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Cell
Article . 2008
License: Elsevier Non-Commercial
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Cell
Article . 2008 . Peer-reviewed
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NFATc1 Balances Quiescence and Proliferation of Skin Stem Cells

Authors: Horsley, Valerie; Aliprantis, Antonios O.; Polak, Lisa; Glimcher, Laurie H.; Fuchs, Elaine;

NFATc1 Balances Quiescence and Proliferation of Skin Stem Cells

Abstract

Quiescent adult stem cells reside in specialized niches where they become activated to proliferate and differentiate during tissue homeostasis and injury. How stem cell quiescence is governed is poorly understood. We report here that NFATc1 is preferentially expressed by hair follicle stem cells in their niche, where its expression is activated by BMP signaling upstream and it acts downstream to transcriptionally repress CDK4 and maintain stem cell quiescence. As stem cells become activated during hair growth, NFATc1 is downregulated, relieving CDK4 repression and activating proliferation. When calcineurin/NFATc1 signaling is suppressed, pharmacologically or via complete or conditional NFATc1 gene ablation, stem cells are activated prematurely, resulting in precocious follicular growth. Our findings may explain why patients receiving cyclosporine A for immunosuppressive therapy display excessive hair growth, and unveil a functional role for calcium-NFATc1-CDK4 circuitry in governing stem cell quiescence.

Keywords

Down-Regulation, Gene Expression, Mice, Nude, Antigens, CD34, CELLCYCLE, Mice, Genes, Reporter, Animals, Cells, Cultured, Cell Proliferation, Cell Nucleus, Mice, Knockout, Biochemistry, Genetics and Molecular Biology(all), Cyclin-Dependent Kinase 4, Gene Expression Regulation, Developmental, Embryo, Mammalian, STEMCELL, Immunohistochemistry, Cyclosporine, Hair Follicle, Biomarkers, Gene Deletion, Immunosuppressive Agents

  • BIP!
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    selected citations
    These citations are derived from selected sources.
    This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
    400
    popularity
    This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
    Top 1%
    influence
    This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
    Top 1%
    impulse
    This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
    Top 1%
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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
400
Top 1%
Top 1%
Top 1%
hybrid