Laminin-332 and-511 in skin

被引:94
作者
Sugawara, Koji [1 ]
Tsuruta, Daisuke [1 ]
Ishii, Masamitsu [1 ]
Jones, Jonathan C. R. [2 ]
Kobayashi, Hiromi [1 ]
机构
[1] Osaka City Univ, Grad Sch Med, Dept Dermatol, Abeno Ku, Osaka 5458585, Japan
[2] NW Univ Feinberg, Feinberg Sch Med, Dept Cell & Mol Biol, Chicago, IL USA
关键词
cancer; extracellular matrix; hair; integrin; laminin;
D O I
10.1111/j.1600-0625.2008.00721.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
The extracellular matrix (ECM) was long thought to be merely a structural tissue support and/or a filter. However, recent studies have suggested that ECM proteins regulate many intracellular and extracellular events, including cell growth, cell adhesion, cell division, cell movement, and apoptosis. They do so through activation of several families of cell surface receptor, including the integrins and syndecans. The focus of this review is on two laminin isoforms expressed in the skin. Laminins are an important molecular component of the basement membranes in a variety of tissue types. They have a cruciform shape, and are composed of three chains-alpha, beta, and gamma. Keratinocytes of the skin secrete numerous laminin isoforms, including laminin-511 and laminin-332. The latter are known to affect the behaviour of keratinocytes through binding to membrane-penetrating receptors (outside-in signal transduction). Conversely, the expression, secretion and assembly of laminin-rich matrices is regulated by cell surface receptors through inside-out signal transduction. We will review how integrins regulate laminin matrix assembly and the signals elicited by laminins that support either migration or stable adhesion of keratinocytes. We will also discuss recent data indicating that laminins plays key regulatory roles in the development of skin appendages and contribute to the pathogenesis of skin cancer.
引用
收藏
页码:473 / 480
页数:8
相关论文
共 88 条
[1]   Differential regulation of α6β4 integrin by PKC isoforms in murine skin keratinocytes [J].
Alt, A ;
Gartsbein, M ;
Ohba, M ;
Kuroki, T ;
Tennenbaum, T .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2004, 314 (01) :17-23
[2]   Bone morphogenetic protein 1 is an extracellular processing enzyme of the laminin 5 γ2 chain [J].
Amano, S ;
Scott, IC ;
Takahara, K ;
Koch, M ;
Champliaud, MF ;
Gerecke, DR ;
Keene, DR ;
Hudson, DL ;
Nishiyama, T ;
Lee, S ;
Greenspan, DS ;
Burgeson, RE .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (30) :22728-22735
[3]   The role of laminins in basement membrane function [J].
Aumailley, M ;
Smyth, N .
JOURNAL OF ANATOMY, 1998, 193 :1-21
[4]   A simplified laminin nomenclature [J].
Aumailley, M ;
Bruckner-Tuderman, L ;
Carter, WG ;
Deutzmann, R ;
Edgar, D ;
Ekblom, P ;
Engel, J ;
Engvall, E ;
Hohenester, E ;
Jones, JCR ;
Kleinman, HK ;
Marinkovich, MP ;
Martin, GR ;
Mayer, U ;
Meneguzzi, G ;
Miner, JH ;
Miyazaki, K ;
Patarroyo, M ;
Paulsson, M ;
Quaranta, V ;
Sanes, JR ;
Sasaki, T ;
Sekiguchi, K ;
Sorokin, LM ;
Talts, JF ;
Tryggvason, K ;
Uitto, J ;
Virtanen, I ;
von der Mark, K ;
Wewer, UM ;
Yamada, Y ;
Yurchenco, PD .
MATRIX BIOLOGY, 2005, 24 (05) :326-332
[5]   Syndecan-1 interaction with the LG4/5 domain in laminin-332 is essential for keratinocyte migration [J].
Bachy, Sophie ;
Letourneur, Francois ;
Rousselle, Patricia .
JOURNAL OF CELLULAR PHYSIOLOGY, 2008, 214 (01) :238-249
[6]   Membrane type 1 matrix metalloprotease cleaves laminin-10 and promotes prostate cancer cell migration [J].
Bair, EL ;
Chen, ML ;
McDaniel, K ;
Sekiguchi, K ;
Cress, AE ;
Nagle, RB ;
Bowden, GT .
NEOPLASIA, 2005, 7 (04) :380-389
[7]   Structure sand function of hemidesmosomes: More than simple adhesion complexes [J].
Borradori, L ;
Sonnenberg, A .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1999, 112 (04) :411-418
[8]   Skin and hair follicle integrity is crucially dependent on β1 integrin expression on keratinocytes [J].
Brakebusch, C ;
Grose, R ;
Quondamatteo, F ;
Ramirez, A ;
Jorcano, JL ;
Pirro, A ;
Svensson, M ;
Herken, R ;
Sasaki, T ;
Timpl, R ;
Werner, S ;
Fässler, R .
EMBO JOURNAL, 2000, 19 (15) :3990-4003
[9]  
CARTER BZ, 1991, LAB INVEST, V65, P610
[10]   Human amnion contains a novel laminin variant, laminin 7, which like laminin 6, covalently associates with laminin 5 to promote stable epithelial-stromal attachment [J].
Champliaud, MF ;
Lunstrum, GP ;
Rousselle, P ;
Nishiyama, T ;
Keene, DR ;
Burgeson, RE .
JOURNAL OF CELL BIOLOGY, 1996, 132 (06) :1189-1198