Title of article
TRP Channel Regulates EGFR Signaling in Hair Morphogenesis and Skin Barrier Formation
Author/Authors
Xiping Cheng، نويسنده , , Jie Jin، نويسنده , , Lily Hu Owen Tam Patrick Lo، نويسنده , , Dongbiao Shen، نويسنده , , XIANPING DONG، نويسنده , , Mohammad A. Samie، نويسنده , , Jayne Knoff، نويسنده , , Brian Eisinger، نويسنده , , Mei-ling Liu، نويسنده , , Susan M. Huang، نويسنده , , Michael J. Caterina، نويسنده , , Peter Dempsey، نويسنده , , Lowell Evan Michael، نويسنده , , Andrzej A. Dlugosz، نويسنده , , Nancy C. Andrews، نويسنده , , David E. Clapham، نويسنده , , Haoxing Xu، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2010
Pages
13
From page
331
To page
343
Abstract
A plethora of growth factors regulate keratinocyte proliferation and differentiation that control hair morphogenesis and skin barrier formation. Wavy hair phenotypes in mice result from naturally occurring loss-of-function mutations in the genes for TGF-α and EGFR. Conversely, excessive activities of TGF-α/EGFR result in hairless phenotypes and skin cancers. Unexpectedly, we found that mice lacking the Trpv3 gene also exhibit wavy hair coat and curly whiskers. Here we show that keratinocyte TRPV3, a member of the transient receptor potential (TRP) family of Ca2+-permeant channels, forms a signaling complex with TGF-α/EGFR. Activation of EGFR leads to increased TRPV3 channel activity, which in turn stimulates TGF-α release. TRPV3 is also required for the formation of the skin barrier by regulating the activities of transglutaminases, a family of Ca2+-dependent crosslinking enzymes essential for keratinocyte cornification. Our results show that a TRP channel plays a role in regulating growth factor signaling by direct complex formation.
Journal title
CELL
Serial Year
2010
Journal title
CELL
Record number
1022093
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