New players tip the scales in the balance between excitatory and inhibitory synapses

被引:30
作者
Levinson, Joshua N. [1 ]
El-Husseini, Alaa [1 ]
机构
[1] Univ British Columbia, Dept Psychiat, Brain Res Ctr, Vancouver, BC V6T 1Z3, Canada
来源
MOLECULAR PAIN | 2005年 / 1卷
关键词
D O I
10.1186/1744-8069-1-12
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Synaptogenesis is a highly controlled process, involving a vast array of players which include cell adhesion molecules, scaffolding and signaling proteins, neurotransmitter receptors and proteins associated with the synaptic vesicle machinery. These molecules cooperate in an intricate manner on both the pre- and postsynaptic sides to orchestrate the precise assembly of neuronal contacts. This is an amazing feat considering that a single neuron receives tens of thousands of synaptic inputs but virtually no mismatch between pre- and postsynaptic components occur in vivo. One crucial aspect of synapse formation is whether a nascent synapse will develop into an excitatory or inhibitory contact. The tight control of a balance between the types of synapses formed regulates the overall neuronal excitability, and is thus critical for normal brain function and plasticity. However, little is known about how this balance is achieved. This review discusses recent findings which provide clues to how neurons may control excitatory and inhibitory synapse formation, with focus on the involvement of the neuroligin family and PSD-95 in this process.
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页数:6
相关论文
共 41 条
[1]   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
[2]   Activity-dependent transcription regulation of PSD-95 by neuregulin-1 and Eos [J].
Bao, JX ;
Lin, H ;
Ouyang, Y ;
Lei, DB ;
Osman, A ;
Kim, TW ;
Mei, L ;
Dai, PG ;
Ohlemiller, KK ;
Ambron, RT .
NATURE NEUROSCIENCE, 2004, 7 (11) :1250-1258
[3]   Synaptic cell adhesion proteins and synaptogenesis in the mammalian central nervous system [J].
Brose, N .
NATURWISSENSCHAFTEN, 1999, 86 (11) :516-524
[4]   GABAergic terminals are required for postsynaptic clustering of dystrophin but not of GABAA receptors and gephyrin [J].
Brünig, I ;
Suter, A ;
Knuesel, I ;
Lüscher, B ;
Fritschy, JM .
JOURNAL OF NEUROSCIENCE, 2002, 22 (12) :4805-4813
[5]   A tripartite protein complex with the potential to couple synaptic vesicle exocytosis to cell adhesion in brain [J].
Butz, S ;
Okamoto, M ;
Südhof, TC .
CELL, 1998, 94 (06) :773-782
[6]   Stargazin regulates synaptic targeting of AMPA receptors by two distinct mechanisms [J].
Chen, L ;
Chetkovich, DM ;
Petralia, RS ;
Sweeney, NT ;
Kawasaki, Y ;
Wenthold, RJ ;
Bredt, DS ;
Nicoll, RA .
NATURE, 2000, 408 (6815) :936-943
[7]   Control of excitatory and inhibitory synapse formation by neuroligins [J].
Chih, B ;
Engelman, H ;
Scheiffele, P .
SCIENCE, 2005, 307 (5713) :1324-1328
[8]   Disorder-associated mutations lead to functional inactivation of neuroligins [J].
Chih, B ;
Afridi, SK ;
Clark, L ;
Scheiffele, P .
HUMAN MOLECULAR GENETICS, 2004, 13 (14) :1471-1477
[9]   The Arg451Cys-neuroligin-3 mutation associated with autism reveals a defect in protein processing [J].
Comoletti, D ;
De Jaco, A ;
Jennings, LL ;
Flynn, RE ;
Gaietta, G ;
Tsigelny, I ;
Ellisman, MH ;
Taylor, P .
JOURNAL OF NEUROSCIENCE, 2004, 24 (20) :4889-4893
[10]  
El-Hussein AE, 2000, SCIENCE, V290, P1364