The Kindlins:: Subcellular localization and expression during murine development

被引:205
|
作者
Ussar, Siegfried
Wang, Hao-Ven
Linder, Stefan
Faessler, Reinhard
Moser, Markus [1 ]
机构
[1] Max Planck Inst Biochem, Dept Mol Med, D-82152 Martinsried, Germany
[2] Univ Munich, Inst Prophylaxe & Epidemiol Kreislaufkrankheiten, D-80336 Munich, Germany
关键词
Kindler syndrome; Integrins; cell-cell adhesion; cell-matrix adhesion;
D O I
10.1016/j.yexcr.2006.06.030
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The three Kindlins are a novel family of focal adhesion proteins. The Kindlin-1 (URP1) gene is mutated in Kindler syndrome, the first skin blistering disease affecting actin attachment in basal keratinocytes. Kindlin-2 (Mig-2), the best studied member of this family, binds ILK and Migfilin, which links Kindlin-2 to the actin cytoskeleton. Kindlin-3 is expressed in hematopoietic cells. Here we describe the genomic organization, gene expression and subcellular localization of murine Kindlins-1 to -3. In situ hybridizations showed that Kindlin-1 is preferentially expressed in epithelia, and Kindlin-2 in striated and smooth muscle cells. Kindlins-1 and -2 are both expressed in the epidermis. While both localize to integrin-mediated adhesion sites in cultured keratinocytes Kindlin-2, but not Kindlin-1, colocalizes with E-cadherin to cell-cell contacts in differentiated keratinocytes. Using a Kindlin-3-specific antiserum and an EGFP-tagged Kindlin-3 construct, we could show that Kindlin-3 is present in the F-actin surrounding ring structure of podosomes, which are specialized adhesion structures of hematopoietic cells. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:3142 / 3151
页数:10
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