Eph signaling: a structural view

被引:149
作者
Himanen, JP [1 ]
Nikolov, DB [1 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Cellular Biochem & Biophys Program, New York, NY 10021 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1016/S0166-2236(02)00005-X
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Eph receptors, the largest subfamily of receptor tyrosine kinases, and their ephrin ligands are important mediators of cell-cell communication regulating cell attachment, shape and mobility. Both Ephs and ephrins are membrane-bound and their interactions at sites of cell-cell contact initiate unique bidirectional signaling cascades, with information transduced in both the receptor-expressing and the ligand-expressing cells. Recent structural and biophysical studies summarized in this review reveal unique molecular features not previously observed in any other receptor-ligand families and explain many of the biochemical and signaling properties of Ephs and ephrins. Of particular importance is the insight into how approximation of ligand-expressing and receptor-expressing cells could lead to the formation and activation of highly ordered signaling centers at cell-cell interfaces.
引用
收藏
页码:46 / 51
页数:6
相关论文
共 65 条
[1]   Roles of ephrinB ligands and EphB receptors in cardiovascular development: demarcation of arterial/venous domains, vascular morphogenesis, and sprouting angiogenesis [J].
Adams, RH ;
Wilkinson, GA ;
Weiss, C ;
Diella, F ;
Gale, NW ;
Deutsch, U ;
Risau, W ;
Klein, R .
GENES & DEVELOPMENT, 1999, 13 (03) :295-306
[2]   Self-association studies on the EphB2 receptor SAM domain using analytical ultracentrifugation [J].
Behlke, J ;
Labudde, D ;
Ristau, O .
EUROPEAN BIOPHYSICS JOURNAL WITH BIOPHYSICS LETTERS, 2001, 30 (06) :411-415
[3]  
BOYD AW, 2001, SCI STKE, V112, pRE20
[4]   EphrinB ligands recruit GRIP family PDZ adaptor proteins into raft membrane microdomains [J].
Brückner, K ;
Labrador, JP ;
Scheiffele, P ;
Herb, A ;
Seeburg, PH ;
Klein, R .
NEURON, 1999, 22 (03) :511-524
[5]   The junction-associated protein AF-6 interacts and clusters with specific EPH receptor tyrosine kinases at specialized sites of cell-cell contact in the brain [J].
Buchert, M ;
Schneider, S ;
Meskenaite, V ;
Adams, MT ;
Canaani, E ;
Baechi, T ;
Moelling, K ;
Hovens, CM .
JOURNAL OF CELL BIOLOGY, 1999, 144 (02) :361-371
[6]   Disruption of Eph/ephrin signaling affects migration and proliferation in the adult subventricular zone [J].
Conover, JC ;
Doetsch, F ;
Garcia-Verdugo, JM ;
Gale, NW ;
Yancopoulos, GD ;
Alvarez-Buylla, A .
NATURE NEUROSCIENCE, 2000, 3 (11) :1091-1097
[7]   EphB2 guides axons at the midline and is necessary for normal vestibular function [J].
Cowan, CA ;
Yokoyama, N ;
Bianchi, LM ;
Henkemeyer, M ;
Fritzsch, B .
NEURON, 2000, 26 (02) :417-430
[8]   EphB receptors interact with NMDA receptors and regulate excitatory synapse formation [J].
Dalva, MB ;
Takasu, MA ;
Lin, MZ ;
Shamah, SM ;
Hu, L ;
Gale, NW ;
Greenberg, ME .
CELL, 2000, 103 (06) :945-956
[9]   LIGANDS FOR EPH-RELATED RECEPTOR TYROSINE KINASES THAT REQUIRE MEMBRANE ATTACHMENT OR CLUSTERING FOR ACTIVITY [J].
DAVIS, S ;
GALE, NW ;
ALDRICH, TH ;
MAISONPIERRE, PC ;
LHOTAK, V ;
PAWSON, T ;
GOLDFARB, M ;
YANCOPOULOS, GD .
SCIENCE, 1994, 266 (5186) :816-819
[10]   Eph receptors and ephrin ligands: embryogenesis to tumorigenesis [J].
Dodelet, VC ;
Pasquale, EB .
ONCOGENE, 2000, 19 (49) :5614-5619