Specification of synaptic connectivity by cell surface interactions

被引:220
作者
de Wit, Joris [1 ,2 ]
Ghosh, Anirvan [3 ]
机构
[1] Katholieke Univ Leuven, VIB Ctr Biol Dis, B-3000 Louvain, Belgium
[2] Katholieke Univ Leuven, Ctr Human Genet, B-3000 Louvain, Belgium
[3] F Hoffmann La Roche & Cie AG, Roche Innovat Ctr Basel, Neurosci Discovery, CH-4070 Basel, Switzerland
基金
欧洲研究理事会; 美国国家卫生研究院;
关键词
TRANSLATIONAL PROFILING APPROACH; LAMINA-RESTRICTED PROJECTION; RETINAL GANGLION-CELLS; RICH REPEAT PROTEINS; N-CADHERIN; MOLECULAR-MECHANISMS; GAMMA-PROTOCADHERINS; CLASSIC CADHERINS; DIFFERENTIAL EXPRESSION; ALPHA-NEUREXINS;
D O I
10.1038/nrn.2015.3
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
The molecular diversification of cell surface molecules has long been postulated to impart specific surface identities on neuronal cell types. The existence of unique cell surface identities would allow neurons to distinguish one another and connect with their appropriate target cells. Although progress has been made in identifying cell type-specific surface molecule repertoires and in characterizing their extracellular interactions, determining how this molecular diversity contributes to the precise wiring of neural circuitry has proven challenging. Here, we review the role of the cadherin, neurexin, immunoglobulin and leucine-rich repeat protein superfamilies in the specification of connectivity. The emerging evidence suggests that the concerted actions of these proteins may critically contribute to the assembly of neural circuits.
引用
收藏
页码:22 / 35
页数:14
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