Trans-synaptic interactions of ionotropic glutamate receptors

被引:5
|
作者
Fossati, Matteo [1 ,2 ]
Charrier, Cecile [3 ]
机构
[1] CNR Inst Neurosci, Via Manzoni 56, I-20089 Rozzano, MI, Italy
[2] Humanitas Clin & Res Ctr IRCCS, Via Manzoni 56, I-20089 Rozzano, MI, Italy
[3] PSL Res Univ, Inst Biol, Ecole Normale Super, INSERM,Ecole Normale Super IBENS,CNRS, F-75005 Paris, France
基金
欧洲研究理事会;
关键词
KAINATE RECEPTORS; SYNAPSE FORMATION; STRUCTURAL BASIS; CELL SYNAPSES; N-CADHERIN; SPECIFICITY; DELTA-2; SRGAP2; GLUD1; CBLN1;
D O I
10.1016/j.conb.2020.09.001
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Trans-synaptic interactions organize the multiple steps of synaptic development and are critical to generate fully functional neuronal circuits. While trans-synaptic interactions are primarily mediated by cell adhesion molecules (CAMs), some directly involve ionotropic glutamate receptors (iGluRs). Here, we review the expanding extracellular and trans-synaptic proteome of iGluRs. We discuss the role of these molecular networks in specifying the formation of excitatory and inhibitory circuits and in the input-specific recruitment of iGluRs at synapses in various cell types and brain regions. We also shed light on human-specific mutations affecting iGluR-mediated trans-synaptic interactions that may provide unique features to the human brain and contribute to its susceptibility to neurodevelopmental disorders. Together, these data support a view in which iGluR function goes far beyond fast excitatory synaptic transmission by shaping the wiring and the functional properties of neural circuits.
引用
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页码:85 / 92
页数:8
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