Postsynaptic signaling at glutamatergic synapses as therapeutic targets

被引:6
|
作者
Ge, Yang [1 ,2 ]
Wang, Yu Tian [1 ,2 ]
机构
[1] Univ British Columbia, Djavad Mowafaghian Ctr Brain Hlth, 2215 Wesbrook Mall, Vancouver, BC V6T 1Z7, Canada
[2] Univ British Columbia, Dept Med, 2775 Laurel St,10th Floor, Vancouver, BC V5Z 1M9, Canada
基金
加拿大健康研究院;
关键词
DISRUPTING NNOS-PSD95 INTERACTION; AMPA RECEPTORS; BRAIN-DAMAGE; PDZ DOMAIN; DAPK1; GLUN2B; ENDOCYTOSIS; PLASTICITY; DISCOVERY; BEHAVIOR;
D O I
10.1016/j.conb.2022.102585
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Dysregulation of glutamatergic synapses plays an important role in the pathogenesis of neurological diseases. In addition to mediating excitatory synaptic transmission, postsynaptic glutamate receptors interact with various membrane and intracellular proteins. They form structural and/or signaling synaptic protein complexes and thereby play diverse postsynaptic functions. Recently, several postsynaptic protein complexes have been associated with various neurological diseases and hence, have been characterized as important therapeutic targets. Moreover, novel small molecules and therapeutic peptides targeting and modulating the activities of these protein complexes have been discovered, some of which have advanced through preclinical translational research and/or clinical studies. This article describes the recent investigation of eight key protein complexes associated with the postsynaptic ionotropic and metabotropic glutamate receptors as therapeutic targets for central nervous system diseases.
引用
收藏
页数:10
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