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Cell Stem Cell
Article
License: Elsevier Non-Commercial
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Cell Stem Cell
Article . 2009
License: Elsevier Non-Commercial
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Cell Stem Cell
Article . 2009 . Peer-reviewed
License: Elsevier Non-Commercial
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TAp63 Prevents Premature Aging by Promoting Adult Stem Cell Maintenance

Authors: Young Jin Gi; Maryline Paris; Min Soon Cho; Satrajit Sinha; Larysa H. Pevny; Freda D. Miller; Jeff Biernaskie; +5 Authors

TAp63 Prevents Premature Aging by Promoting Adult Stem Cell Maintenance

Abstract

The cellular mechanisms that regulate the maintenance of adult tissue stem cells are still largely unknown. We show here that the p53 family member, TAp63, is essential for maintenance of epidermal and dermal precursors and that, in its absence, these precursors senesce and skin ages prematurely. Specifically, we have developed a TAp63 conditional knockout mouse and used it to ablate TAp63 in the germline (TAp63−/−) or in K14-expressing cells in the basal layer of the epidermis (TAp63fl/fl;K14cre+). TAp63−/− mice age prematurely and develop blisters, skin ulcerations, senescence of hair follicle-associated dermal and epidermal cells, and decreased hair morphogenesis. These phenotypes are likely due to loss of TAp63 in dermal and epidermal precursors since both cell types show defective proliferation, early senescence, and genomic instability. These data indicate that TAp63 serves to maintain adult skin stem cells by regulating cellular senescence and genomic stability, thereby preventing premature tissue aging.

Keywords

Keratinocytes, Mice, Knockout, Wound Healing, Aging, Premature, Cell Biology, Dermis, Genes, p53, Phosphoproteins, STEMCELL, Genomic Instability, Skin Aging, Adult Stem Cells, Mice, Epidermal Cells, Genetics, Trans-Activators, Molecular Medicine, Animals, Hair Follicle, Cellular Senescence, DNA Damage

  • BIP!
    Impact byBIP!
    citations
    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).
    231
    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 10%
    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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citations
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!
231
Top 1%
Top 10%
Top 1%
hybrid