Synaptic Neurexin Complexes: A Molecular Code for the Logic of Neural Circuits

被引:517
作者
Sudhof, Thomas C. [1 ,2 ]
机构
[1] Stanford Univ, Med Sch, Dept Mol & Cellular Physiol, 265 Campus Dr, Stanford, CA 94305 USA
[2] Stanford Univ, Howard Hughes Med Inst, Med Sch, 265 Campus Dr, Stanford, CA 94305 USA
关键词
CELL-ADHESION MOLECULE; GLUTAMATE-RECEPTOR DELTA-2; ALPHA-LATROTOXIN RECEPTOR; ATTENTION-DEFICIT/HYPERACTIVITY DISORDER; REPEAT TRANSMEMBRANE PROTEINS; FAMILY MESSENGER-RNAS; LONG-TERM DEPRESSION; INHIBITORY SYNAPSES; CBLN FAMILY; PRESYNAPTIC NEUREXIN-3;
D O I
10.1016/j.cell.2017.10.024
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
Synapses are specialized junctions between neurons in brain that transmit and compute information, thereby connecting neurons into millions of overlapping and interdigitated neural circuits. Here, we posit that the establishment, properties, and dynamics of synapses are governed by a molecular logic that is controlled by diverse trans-synaptic signaling molecules. Neurexins, expressed in thousands of alternatively spliced isoforms, are central components of this dynamic code. Presynaptic neurexins regulate synapse properties via differential binding to multifarious postsynaptic ligands, such as neuroligins, cerebellin/GluD complexes, and latrophilins, thereby shaping the input/output relations of their resident neural circuits. Mutations in genes encoding neurexins and their ligands are associated with diverse neuropsychiatric disorders, especially schizophrenia, autism, and Tourette syndrome. Thus, neurexins nucleate an overall trans-synaptic signaling network that controls synapse properties, which thereby determines the precise responses of synapses to spike patterns in a neuron and circuit and which is vulnerable to impairments in neuropsychiatric disorders.
引用
收藏
页码:745 / 769
页数:25
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