Human epidermal stem cell function is regulated by circadian oscillations

Human skin copes with harmful environmental factors that are circadian in nature, yet how circadian rhythms modulate the function of human epidermal stem cells is mostly unknown. Here we show that in human epidermal stem cells and their differentiated counterparts, core clock genes peak in a success...

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Detalles Bibliográficos
Autores: Janich, Peggy, 1981-, Toufighi, Kiana, 1980-, Solanas, Guiomar, Luis, Nuno Miguel, 1982-, Minkwitz, Susann, Serrano Pubull, Luis, 1982-, Lehner, Ben, 1978-, Aznar Benitah, Salvador
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2013
País:España
Institución:Universitat Pompeu Fabra
Repositorio:Repositorio Digital de la UPF
OAI Identifier:oai:repositori.upf.edu:10230/23118
Acceso en línea:http://hdl.handle.net/10230/23118
http://dx.doi.org/10.1016/j.stem.2013.09.004
Access Level:acceso abierto
Palabra clave:Ritmes circadiaris -- Efectes fisiològics
Epidermis -- Citologia
Cèl·lules mare -- Citologia
Descripción
Sumario:Human skin copes with harmful environmental factors that are circadian in nature, yet how circadian rhythms modulate the function of human epidermal stem cells is mostly unknown. Here we show that in human epidermal stem cells and their differentiated counterparts, core clock genes peak in a successive and phased manner, establishing distinct temporal intervals during the 24 hr day period. Each of these successive clock waves is associated with a peak in the expression of subsets of transcripts that temporally segregate the predisposition of epidermal stem cells to respond to cues that regulate their proliferation or differentiation, such as TGFβ and calcium. Accordingly, circadian arrhythmia profoundly affects stem cell function in culture and in vivo. We hypothesize that this intricate mechanism ensures homeostasis by providing epidermal stem cells with environmentally relevant temporal functional cues during the course of the day and that its perturbation may contribute to aging and carcinogenesis.