Distinct contribution of stem and progenitor cells to epidermal maintenance

被引:0
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作者
Guilhem Mascré
Sophie Dekoninck
Benjamin Drogat
Khalil Kass Youssef
Sylvain Brohée
Panagiota A. Sotiropoulou
Benjamin D. Simons
Cédric Blanpain
机构
[1] Université Libre de Bruxelles,Department of Physics
[2] IRIBHM,undefined
[3] Brussels B-1070,undefined
[4] Belgium ,undefined
[5] Université Libre de Bruxelles,undefined
[6] Machine Learning Group,undefined
[7] Brussels B-1050,undefined
[8] Belgium ,undefined
[9] Cavendish Laboratory,undefined
[10] J. J. Thomson Avenue,undefined
[11] Cambridge CB3 0HE,undefined
[12] UK,undefined
[13] The Wellcome Trust/Cancer Research UK Gurdon Institute,undefined
[14] University of Cambridge,undefined
[15] Tennis Court Road,undefined
[16] Cambridge CB2 1QN,undefined
[17] UK ,undefined
[18] WELBIO,undefined
[19] Université Libre de Bruxelles,undefined
[20] Brussels B-1070,undefined
[21] Belgium ,undefined
来源
Nature | 2012年 / 489卷
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摘要
The skin interfollicular epidermis (IFE) is the first barrier against the external environment and its maintenance is critical for survival. Two seemingly opposite theories have been proposed to explain IFE homeostasis. One posits that IFE is maintained by long-lived slow-cycling stem cells that give rise to transit-amplifying cell progeny, whereas the other suggests that homeostasis is achieved by a single committed progenitor population that balances stochastic fate. Here we probe the cellular heterogeneity within the IFE using two different inducible Cre recombinase–oestrogen receptor constructs targeting IFE progenitors in mice. Quantitative analysis of clonal fate data and proliferation dynamics demonstrate the existence of two distinct proliferative cell compartments arranged in a hierarchy involving slow-cycling stem cells and committed progenitor cells. After wounding, only stem cells contribute substantially to the repair and long-term regeneration of the tissue, whereas committed progenitor cells make a limited contribution.
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页码:257 / 262
页数:5
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