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Published online
doi:10.1083/jcb.200907080
The Journal of Cell Biology, Vol. 187, No. 1, 91-100
The Rockefeller University Press, 0021-9525 $30.00
© Van Keymeulen et al.
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Epidermal progenitors give rise to Merkel cells during embryonic development and adult homeostasis



Alexandra Van Keymeulen1, Guilhem Mascre1, Khalil Kass Youseff1, Itamar Harel2, Cindy Michaux1, Natalie De Geest3,4, Caroline Szpalski1, Younes Achouri5, Wilhelm Bloch6, Bassem A. Hassan3,4, and Cédric Blanpain1

1 Institut de Recherche Interdisciplinaire en Biologie Humaine et Moléculaire, Université Libre de Bruxelles, Brussels B-1070, Belgium
2 Weizmann Institute of Science, Rehovot 76100, Israel
3 Vlaams Institute for Biotechnology Department of Molecular and Developmental Genetics, 4 Centre for Human Genetics, Catholic University Leuven, 3000 Leuven, Belgium
5 Université catholique de Louvain, Institut de Duve, Brussels B-1200, Belgium
6 Section of Molecular and Cellular Sport Medicine, German Sport University Cologne, D-50933 Cologne, Germany

Correspondence to Cédric Blanpain: Cedric.Blanpain{at}ulb.ac.be

Merkel cells (MCs) are located in the touch-sensitive area of the epidermis and mediate mechanotransduction in the skin. Whether MCs originate from embryonic epidermal or neural crest progenitors has been a matter of intense controversy since their discovery >130 yr ago. In addition, how MCs are maintained during adulthood is currently unknown. In this study, using lineage-tracing experiments, we show that MCs arise through the differentiation of epidermal progenitors during embryonic development. In adults, MCs undergo slow turnover and are replaced by cells originating from epidermal stem cells, not through the proliferation of differentiated MCs. Conditional deletion of the Atoh1/Math1 transcription factor in epidermal progenitors results in the absence of MCs in all body locations, including the whisker region. Our study demonstrates that MCs arise from the epidermis by an Atoh1-dependent mechanism and opens new avenues for study of MC functions in sensory perception, neuroendocrine signaling, and MC carcinoma.


Abbreviations used in this paper: cKO, conditional knockout; CREER, estrogen receptor–inducible CRE; CREPR, Cre progesterone receptor fusion protein; HF, hair follicle; MC, Merkel cell; NCC, neural crest cell; P-cadherin, placental cadherin; SC, stem cell; TAM, tamoxifen.

© 2009 Van Keymeulen et al.
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Merkel cells bear the touch of epidermis
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