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TRP Channel Regulates EGFR Signaling in Hair Morphogenesis and Skin Barrier Formation

机译:TRP通道调节毛发形态发生和皮肤屏障形成中的EGFR信号传导

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摘要

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-a and EGFR. Conversely, excessive activities of TGF-a/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-a/EGFR. Activation of EGFR leads to increased TRPV3 channel activity, which in turn stimulates TGF-a 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.
机译:大量的生长因子调节角质形成细胞的增殖和分化,从而控制头发的形态发生和皮肤屏障的形成。小鼠中的波浪状头发表型是由TGF-α和EGFR基因中自然发生的功能丧失突变引起的。相反,TGF-α/ EGFR的过度活性导致无毛表型和皮肤癌。出乎意料的是,我们发现缺少Trpv3基因的小鼠还表现出波浪状的毛发和卷曲的胡须。在这里,我们显示角质形成细胞TRPV3是Ca2 +渗透通道的瞬时受体电位(TRP)家族的成员,与TGF-α/ EGFR形成信号复合物。 EGFR的激活导致TRPV3通道活性增加,进而刺激TGF-α释放。 TRPV3也是通过调节转谷氨酰胺酶的活性来形成皮肤屏障所必需的,转谷氨酰胺酶是角化细胞角质化必不可少的一系列依赖Ca2 +的交联酶。我们的结果表明,TRP通道通过直接复合物形成在调节生长因子信号传导中起作用。

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