External negative electric potential accelerates exocytosis of lamellar bodies in human skin ex vivo

Exocytosis of lamellar bodies at the uppermost nucleated layer of the epidermis is a crucial process for epidermal permeability barrier homoeostasis. We have previously suggested that skin surface electric potential might be associated with barrier homoeostasis. Thus, we hypothesized that the potent...

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Published inExperimental dermatology Vol. 22; no. 6; pp. 421 - 423
Main Authors Kumamoto, Junichi, Goto, Makiko, Denda, Sumiko, Nakatani, Masashi, Takasugi, Yuya, Tsuchiya, Katsunori, Shimizu, Yuji, Takatsuru, Yusuke, Denda, Mitsuhiro
Format Journal Article
LanguageEnglish
Published Denmark Blackwell Publishing Ltd 01.06.2013
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Summary:Exocytosis of lamellar bodies at the uppermost nucleated layer of the epidermis is a crucial process for epidermal permeability barrier homoeostasis. We have previously suggested that skin surface electric potential might be associated with barrier homoeostasis. Thus, we hypothesized that the potential might drive exocytosis of lamellar bodies. In this study, we tested this idea by applying negative electric potential (−0.5 V) to human skin samples ex vivo for 2 h and observing the ultrastructure of the uppermost layer. The secretion of lamellar bodies was accelerated in the potential‐applied skin, compared to that in untreated control skin. Multiphoton observation indicated that extracellular lipid domains were more extensive in treated skin than in control skin. Moreover, the calcium ion gradient was greater at the uppermost layer of the epidermis of treated skin, compared to that in control skin. These results indicate that electric potential may regulate lamellar body secretion in healthy human skin.
Bibliography:ArticleID:EXD12145
Data S1. Materials and methods.Data S2. Two-photon microscopic observation.Figure S1. Two-photon laser microscopic observation of lipids in human skin tissue loaded or not loaded with negative external electric potential. a: Control skin (Bar = 10 μm), b: Treated skin (Bar = 10 μm). c-g: Sections of control skin at intervals of 1 μm (Bars = 2 μm). h-l: Sections of treated skin at intervals of 1 μm (Bars = 2 μm). Longer intercellular lipid domains were observed in treated skin than in control skin. m: Three-dimensional image of treated skin. Clear intercellular lipid domains can be seen (arrows). The length of each axis is indicated.
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SourceType-Other Sources-1
ObjectType-Article-2
content type line 63
ObjectType-Correspondence-1
ISSN:0906-6705
1600-0625
DOI:10.1111/exd.12145