The Kindlins:: Subcellular localization and expression during murine development

被引:208
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
相关论文
共 22 条
[1]   A novel LIM protein Cal promotes cardiac differentiation by association with CSX/NKX2-5 [J].
Akazawa, H ;
Kudoh, S ;
Mochizuki, N ;
Takekoshi, N ;
Takano, H ;
Nagai, T ;
Komuro, I .
JOURNAL OF CELL BIOLOGY, 2004, 164 (03) :395-405
[2]   Recurrent mutations in kindlin-1, a novel keratinocyte focal contact protein, in the autosomal recessive skin fragility and photosensitivity disorder, Kindler syndrome [J].
Ashton, GHS ;
McLean, WHI ;
South, AP ;
Oyama, N ;
Smith, FJD ;
Al-Suwaid, R ;
Al ismaily, A ;
Atherton, DJ ;
Harwood, CA ;
Leigh, IM ;
Moss, C ;
Didona, B ;
Zambruno, G ;
Patrizi, A ;
Eady, RAJ ;
McGrath, JA .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2004, 122 (01) :78-83
[3]   Proteomic analysis of the cell-surface membrane in chronic lymphocytic leukemia: identification of two novel proteins, BCNP1 and MIG2B [J].
Boyd, RS ;
Adam, PJ ;
Patel, S ;
Loader, JA ;
Berry, J ;
Redpath, NT ;
Poyser, HR ;
Fletcher, GC ;
Burgess, NA ;
Stamps, AC ;
Hudson, L ;
Smith, P ;
Griffiths, M ;
Willis, TG ;
Karran, EL ;
Oscier, DG ;
Catovsky, D ;
Terrett, JA ;
Dyer, MJS .
LEUKEMIA, 2003, 17 (08) :1605-1612
[4]   The phosphotyrosine binding-like domain of talin activates Integrins [J].
Calderwood, DA ;
Yan, BX ;
de Pereda, JM ;
Alvarez, BG ;
Fujioka, Y ;
Liddington, RC ;
Ginsberg, MH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (24) :21749-21758
[5]   The FERM domain: a unique module involved in the linkage of cytoplasmic proteins to the membrane [J].
Chishti, AH ;
Kim, AC ;
Marfatia, SM ;
Lutchman, M ;
Hanspal, M ;
Jindal, H ;
Liu, SC ;
Low, PS ;
Rouleau, GA ;
Mohandas, N ;
Chasis, JA ;
Conboy, JG ;
Gascard, P ;
Takakuwa, Y ;
Huang, SC ;
Benz, EJ ;
Bretscher, A ;
Fehon, RG ;
Gusella, AF ;
Ramesh, V ;
Solomon, F ;
Marchesi, VT ;
Tsukita, S ;
Tsukita, S ;
Arpin, M ;
Louvard, D ;
Tonks, NK ;
Anderson, JM ;
Fanning, AS ;
Bryant, PJ ;
Woods, DF ;
Hoover, KB .
TRENDS IN BIOCHEMICAL SCIENCES, 1998, 23 (08) :281-282
[6]   Structural determinants of integrin recognition by Talin [J].
García-Alvarez, B ;
de Pereda, JM ;
Calderwood, DA ;
Ulmer, TS ;
Critchley, D ;
Campbell, ID ;
Ginsberg, MH ;
Liddington, RC .
MOLECULAR CELL, 2003, 11 (01) :49-58
[7]   Physical and functional association of migfilin with cell-cell adhesions [J].
Gkretsi, V ;
Zhang, YJ ;
Tu, YZ ;
Chen, K ;
Stolz, DB ;
Yang, YQ ;
Watkins, SC ;
Wu, CY .
JOURNAL OF CELL SCIENCE, 2005, 118 (04) :697-710
[8]   Identification of mutations in a new gene encoding a FERM family protein with a pleckstrin homology domain in Kindler syndrome [J].
Jobard, F ;
Bouadjar, B ;
Caux, E ;
Hadj-Rabia, S ;
Has, C ;
Matsuda, E ;
Weissenbach, J ;
Lathrop, M ;
Prud'homme, JF ;
Fischer, J .
HUMAN MOLECULAR GENETICS, 2003, 12 (08) :925-935
[9]   Expression of the mitogen-inducible gene-2 (mig-2) is elevated in human uterine leiomyomas but not in leiomyosarcomas [J].
Kato, K ;
Shiozawa, T ;
Mitsushita, J ;
Toda, A ;
Horiuchi, A ;
Nikaido, T ;
Fujii, S ;
Konishi, I .
HUMAN PATHOLOGY, 2004, 35 (01) :55-60