Mitotic diversity in homeostatic human interfollicular epidermis

Despite decades of skin research, regulation of proliferation and homeostasis in human epidermis is still insufficiently understood. To address the role of mitoses in tissue regulation, we utilized human long-term skin equivalents and systematically assessed mitoses during early epidermal developmen...

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Main Authors: Nöske, Katharina (Author) , Stark, Hans-Jürgen (Author) , Nevaril, Leonard (Author) , Berning, Manuel (Author) , Langbein, Lutz (Author) , Goyal, Ashish (Author) , Diederichs, Sven (Author) , Boukamp, Petra (Author)
Format: Article (Journal)
Language:English
Published: 28 January 2016
In: International journal of molecular sciences
Year: 2016, Volume: 17, Issue: 2, Pages: 167
ISSN:1422-0067
DOI:10.3390/ijms17020167
Online Access:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.3390/ijms17020167
Verlag, lizenzpflichtig, Volltext: https://www.mdpi.com/1422-0067/17/2/167
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Author Notes:Katharina Nöske, Hans-Jürgen Stark, Leonard Nevaril, Manuel Berning, Lutz Langbein, Ashish Goyal, Sven Diederichs and Petra Boukamp
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Summary:Despite decades of skin research, regulation of proliferation and homeostasis in human epidermis is still insufficiently understood. To address the role of mitoses in tissue regulation, we utilized human long-term skin equivalents and systematically assessed mitoses during early epidermal development and long-term epidermal regeneration. We now demonstrate four different orientations: (1) horizontal, i.e., parallel to the basement membrane (BM) and suggestive of symmetric divisions; (2) oblique with an angle of 45°-70°; or (3) perpendicular, suggestive of asymmetric division. In addition, we demonstrate a fourth substantial fraction of suprabasal mitoses, many of which are committed to differentiation (Keratin K10-positive). As verified also for normal human skin, this spatial mitotic organization is part of the regulatory program of human epidermal tissue homeostasis. As a potential marker for asymmetric division, we investigated for Numb and found that it was evenly spread in almost all undifferentiated keratinocytes, but indeed asymmetrically distributed in some mitoses and particularly frequent under differentiation-repressing low-calcium conditions. Numb deletion (stable knockdown by CRISPR/Cas9), however, did not affect proliferation, neither in a three-day follow up study by life cell imaging nor during a 14-day culture period, suggesting that Numb is not essential for the general control of keratinocyte division.
Item Description:Gesehen am 26.06.2020
Physical Description:Online Resource
ISSN:1422-0067
DOI:10.3390/ijms17020167