Desmoglein 1-dependent suppression of EGFR signaling promotes epidermal differentiation and morphogenesis

被引:178
作者
Getsios, Spiro [1 ,2 ,3 ]
Simpson, Cory L. [1 ]
Kojima, Shin-ichiro [3 ]
Harmon, Robert [1 ]
Sheu, Linda J. [1 ]
Dusek, Rachel L. [1 ]
Cornwell, Mona [1 ]
Green, Kathleen J. [1 ,2 ]
机构
[1] Northwestern Univ, Dept Pathol, Feinberg Sch Med, Chicago, IL 60611 USA
[2] Northwestern Univ, Dept Dermatol, Feinberg Sch Med, Chicago, IL 60611 USA
[3] Northwestern Univ, Dept Cell & Mol Biol, Feinberg Sch Med, Chicago, IL 60611 USA
关键词
GROWTH-FACTOR RECEPTOR; E-CADHERIN; HAIR FOLLICLE; KERATINOCYTE DIFFERENTIATION; GENE-TRANSCRIPTION; BULLOUS IMPETIGO; EXPRESSION; SKIN; DESMOSOMES; PEMPHIGUS;
D O I
10.1083/jcb.200809044
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Dsg1 (desmoglein 1) is a member of the cadherin family of Ca2+-dependent cell adhesion molecules that is first expressed in the epidermis as keratinocytes transit out of the basal layer and becomes concentrated in the uppermost cell layers of this stratified epithelium. In this study, we show that Dsg1 is not only required for maintaining epidermal tissue integrity in the superficial layers but also supports keratinocyte differentiation and suprabasal morphogenesis. Dsg1 lacking N-terminal ectodomain residues required for adhesion remained capable of promoting keratinocyte differentiation. Moreover, this capability did not depend on cytodomain interactions with the armadillo protein plakoglobin or coexpression of its companion suprabasal cadherin, Dsc1 ( desmocollin 1). Instead, Dsg1 was required for suppression of epidermal growth factor receptor-Erk1/2 (extracellular signal-regulated kinase 1/2) signaling, thereby facilitating keratinocyte progression through a terminal differentiation program. In addition to serving as a rigid anchor between adjacent cells, this study implicates desmosomal cadherins as key components of a signaling axis governing epithelial morphogenesis.
引用
收藏
页码:1243 / 1258
页数:16
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