Organization of multiprotein complexes at cell-cell junctions

被引:113
作者
Ebnet, Klaus [1 ]
机构
[1] Univ Munster, Ctr Mol Biol & Inflammat ZMBE, Inst Med Biochem, Munster, Germany
关键词
adherens junction; tight junction; cell polarity; cell-cell adhesion; protein complexes; JAM; PAR proteins;
D O I
10.1007/s00418-008-0418-7
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The formation of stable cell-cell contacts is required for the generation of barrier-forming sheets of epithelial and endothelial cells. During various physiological processes like tissue development, wound healing or tumorigenesis, cellular junctions are reorganized to allow the release or the incorporation of individual cells. Cell-cell contact formation is regulated by multiprotein complexes which are localized at specific structures along the lateral cell junctions like the tight junctions and adherens junctions and which are targeted to these site through their association with cell adhesion molecules. Recent evidence indicates that several major protein complexes exist which have distinct functions during junction formation. However, this evidence also indicates that their composition is dynamic and subject to changes depending on the state of junction maturation. Thus, cell-cell contact formation and integrity is regulated by a complex network of protein complexes. Imbalancing this network by oncogenic proteins or pathogens results in barrier breakdown and eventually in cancer. Here, I will review the molecular organization of the major multiprotein complexes at junctions of epithelial cells and discuss their function in cell-cell contact formation and maintenance.
引用
收藏
页码:1 / 20
页数:20
相关论文
共 196 条
[31]   The cell polarity protein ASIP/PAR-3 directly associates with junctional adhesion molecule (JAM) [J].
Ebnet, K ;
Suzuki, A ;
Horikoshi, Y ;
Hirose, T ;
Meyer zu Brickwedde, MK ;
Ohno, S ;
Vestweber, D .
EMBO JOURNAL, 2001, 20 (14) :3738-3748
[32]   The junctional adhesion molecule (JAM) family members JAM-2 and JAM-3 associate with the cell polarity protein PAR-3: a possible role for JAMs in endothelial cell polarity [J].
Ebnet, K ;
Aurrand-Lions, M ;
Kuhn, A ;
Kiefer, F ;
Butz, S ;
Zander, K ;
Brickwedde, MKMZ ;
Suzuki, A ;
Imhof, BA ;
Vestweber, D .
JOURNAL OF CELL SCIENCE, 2003, 116 (19) :3879-3891
[33]   Junctional adhesion molecules (JAMs): more molecules with dual functions? [J].
Ebnet, K ;
Suzuki, A ;
Ohno, S ;
Vestweber, D .
JOURNAL OF CELL SCIENCE, 2004, 117 (01) :19-29
[34]   Isolation and functional characterization of the actin-binding region in the tight junction protein ZO-1 [J].
Fanning, AS ;
Ma, TY ;
Anderson, JM .
FASEB JOURNAL, 2002, 16 (11) :1835-+
[35]   The tight junction protein ZO-1 establishes a link between the transmembrane protein occludin and the actin cytoskeleton [J].
Fanning, AS ;
Jameson, BJ ;
Jesaitis, LA ;
Anderson, JM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (45) :29745-29753
[36]   Multiple regions of Crumbs3 are required for tight junction formation in MCF10A cells [J].
Fogg, VC ;
Liu, CJ ;
Margolis, B .
JOURNAL OF CELL SCIENCE, 2005, 118 (13) :2859-2869
[37]   Socializing with the neighbors: Stem cells and their niche [J].
Fuchs, E ;
Tumbar, T ;
Guasch, G .
CELL, 2004, 116 (06) :769-778
[38]   Involvement of nectin-activated Cdc42 small G protein in organization of adherens and tight junctions in Madin-Darby canine kidney cells [J].
Fukuhara, A ;
Shimizu, K ;
Kawakatsu, T ;
Fukuhara, T ;
Takai, Y .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (51) :51885-51893
[39]   Activation of Cdc42 by trans interactions of the cell adhesion molecules nectins through c-Src and Cdc42-GEF FRG [J].
Fukuhara, T ;
Shimizu, K ;
Kawakatsu, T ;
Fukuyama, T ;
Minami, Y ;
Honda, T ;
Hoshino, T ;
Yamada, T ;
Ogita, H ;
Okada, M ;
Takai, Y .
JOURNAL OF CELL BIOLOGY, 2004, 166 (03) :393-405
[40]   Involvement of the c-Src-Crk-C3G-Rap1 signaling in the nectin-induced activation of Cdc42 and formation of adherens junctions [J].
Fukuyama, T ;
Ogita, H ;
Kawakatsu, T ;
Fukuhara, T ;
Yamada, T ;
Sato, T ;
Shimizu, K ;
Nakamura, T ;
Matsuda, M ;
Takai, Y .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (01) :815-825