Protein tyrosine phosphatases PTPδ, PTPσ, and LAR: presynaptic hubs for synapse organization

被引:211
作者
Takahashi, Hideto [1 ,2 ,3 ]
Craig, Ann Marie [1 ,2 ]
机构
[1] Univ British Columbia, Brain Res Ctr, Vancouver, BC V6T 2B5, Canada
[2] Univ British Columbia, Dept Psychiat, Vancouver, BC V6T 2B5, Canada
[3] Inst Rech Clin Montreal, Montreal, PQ H2W 1R7, Canada
基金
加拿大健康研究院; 美国国家卫生研究院;
关键词
synaptogenesis; neurexin; NGL-3; TrkC; IL1RAPL1; Slitrk; LINKED MENTAL-RETARDATION; CELL-ADHESION MOLECULE; LIPRIN-ALPHA; NEUROTROPHIN RECEPTORS; INTERLEUKIN-1; RECEPTOR; NERVOUS-SYSTEM; RPTP-SIGMA; TRANSSYNAPTIC INTERACTION; DIFFERENTIAL EXPRESSION; POSSIBLE ASSOCIATION;
D O I
10.1016/j.tins.2013.06.002
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Synapse development requires differentiation of presynaptic neurotransmitter release sites and postsynaptic receptive apparatus coordinated by synapse organizing proteins. In addition to the well-characterized neurexins, recent studies identified presynaptic type ha receptor-type protein tyrosine phosphatases (RPTPs) as mediators of presynaptic differentiation and triggers of postsynaptic differentiation, thus extending the roles of RPTPs from axon outgrowth and guidance. Similarly to neurexins, RPTPs exist in multiple isoforms generated by alternative splicing that interact in a splice-selective code with diverse postsynaptic partners. The parallel RPTP and neurexin hub design facilitates synapse self-assembly through cooperation, pairs presynaptic similarity with postsynaptic diversity, and balances excitation with inhibition. Upon mutation of individual genes in neuropsychiatric disorders, imbalance of this synaptic organizing network may contribute to impaired cognitive function.
引用
收藏
页码:522 / 534
页数:13
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