The neuroligin and neurexin families:: from structure to function at the synapse

被引:139
作者
Lise, M-F.
El-Husseini, A. [1 ]
机构
[1] Univ British Columbia, Dept Psychiat, Vancouver, BC V6T 1Z3, Canada
[2] Univ British Columbia, Brain Res Ctr, Vancouver, BC V6T 1Z3, Canada
关键词
synapse formation; cell adhesion molecule; neuroligin; neurexin; scaffolding protein;
D O I
10.1007/s00018-006-6061-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Proper brain connectivity and neuronal transmission rely on the accurate assembly of neurotransmitter receptors, cell adhesion molecules and several other scaffolding and signaling proteins at synapses. Several new exciting findings point to an important role for the neuroligin family of adhesion molecules in synapse development and function. In this review, we summarize current knowledge of the structure of neuroligins and neurexins, their potential binding partners at the synapse. We also discuss their potential involvement in several aspects of synapse development, including induction, specificity and stabilization. The implication of neuroligins in cognitive disorders such as autism and mental retardation is also discussed.
引用
收藏
页码:1833 / 1849
页数:17
相关论文
共 167 条
[1]   Knowing a nascent synapse when you see it [J].
Ahmari, SE ;
Smith, SJ .
NEURON, 2002, 34 (03) :333-336
[2]   Assembly of presynaptic active zones from cytoplasmic transport packets [J].
Ahmari, SE ;
Buchanan, J ;
Smith, SJ .
NATURE NEUROSCIENCE, 2000, 3 (05) :445-451
[3]   Ankyrin-based subcellular gradient of neurofascin, an immunoglobulin family protein, directs GABAergic innervation at Purkinje axon initial segment [J].
Ango, F ;
di Cristo, G ;
Higashiyama, H ;
Bennett, V ;
Wu, P ;
Huang, ZJ .
CELL, 2004, 119 (02) :257-272
[4]   Evidence for allelic association on chromosome 3q25-27 in families with autism spectrum disorders originating from a subisolate of Finland [J].
Auranen, M ;
Varilo, T ;
Alen, R ;
Vanhala, R ;
Ayers, K ;
Kempas, E ;
Ylisaukko-oja, T ;
Peltonen, L ;
Järvelä, I .
MOLECULAR PSYCHIATRY, 2003, 8 (10) :879-884
[5]   A genomewide screen for autism-spectrum disorders:: Evidence for a major susceptibility locus on chromosome 3q25-27 [J].
Auranen, M ;
Vanhala, R ;
Varilo, T ;
Ayers, K ;
Kempas, E ;
Ylisaukko-oja, T ;
Sinsheimer, JS ;
Peltonen, L ;
Järvelä, I .
AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 71 (04) :777-790
[6]   A Drosophila neurexin is required for septate junction and blood-nerve barrier formation and function [J].
Baumgartner, S ;
Littleton, JT ;
Broadie, K ;
Bhat, MA ;
Harbecke, R ;
Lengyel, JA ;
ChiquetEhrismann, R ;
Prokop, A ;
Bellen, HJ .
CELL, 1996, 87 (06) :1059-1068
[7]   Neurexin IV, caspr and paranodin - novel members of the neurexin family: encounters of axons and glia [J].
Bellen, HJ ;
Lu, Y ;
Beckstead, R ;
Bhat, MA .
TRENDS IN NEUROSCIENCES, 1998, 21 (10) :444-449
[8]   Molecular basis of plasticity in the visual cortex [J].
Berardi, N ;
Pizzorusso, T ;
Ratto, GM ;
Maffei, L .
TRENDS IN NEUROSCIENCES, 2003, 26 (07) :369-378
[9]   Axon-glia interactions and the domain organization of myelinated axons requires Neurexin IV/Caspr/Paranodin [J].
Bhat, MA ;
Rios, JC ;
Lu, Y ;
Garcia-Fresco, GP ;
Ching, W ;
St Martin, M ;
Li, JJ ;
Einheber, S ;
Chesler, M ;
Rosenbluth, J ;
Salzer, JL ;
Bellen, HJ .
NEURON, 2001, 30 (02) :369-383
[10]   CASK and protein 4.1 support F-actin nucleation on neurexins. [J].
Biederer, T ;
Südhof, TC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (51) :47869-47876