NGL family PSD-95-interacting adhesion molecules regulate excitatory synapse formation

被引:197
作者
Kim, Seho
Burette, Alain
Chung, Hye Sun
Kwon, Seok-Kyu
Woo, Jooyeon
Lee, Hyun Woo
Kim, Karam
Kim, Hyun
Weinberg, Richard J.
Kim, Eunjoon [1 ]
机构
[1] Korea Adv Inst Sci & Technol, Natl Creat Res Initiat Ctr Synaptogenesis, Taejon 305701, South Korea
[2] Korea Adv Inst Sci & Technol, Dept Biol Sci, Taejon 305701, South Korea
[3] Univ N Carolina, Dept Cell & Dev Biol, Chapel Hill, NC 27599 USA
[4] Korea Univ, Dept Anat, Coll Med, Seoul 136705, South Korea
[5] Korea Univ, Div Brain Korea 21, Coll Med, Seoul 136705, South Korea
[6] Univ N Carolina, Ctr Neurosci, Chapel Hill, NC 27599 USA
关键词
D O I
10.1038/nn1763
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Synaptic cell adhesion molecules (CAMs) regulate synapse formation through their trans-synaptic and heterophilic adhesion. Here we show that postsynaptic netrin-G ligand (NGL)CAMs associate with netrin-G CAMs in an isoform-specific manner and, through their cytosolic tail, with the abundant postsynaptic scaffold postsynaptic density-95 (PSD-95). Overexpression of NGL-2 in cultured rat neurons increased the number of PSD-95-positive dendritic protrusions. NGL-2 located on heterologous cells or beads induced functional presynaptic differentiation in contacting neurites. Direct aggregation of NGL-2 on the surface membrane of dendrites induced the clustering of excitatory postsynaptic proteins. Competitive inhibition by soluble NGL-2 reduced the number of excitatory synapses. NGL-2 knockdown reduced excitatory, but not inhibitory, synapse numbers and currents. These results suggest that NGL regulates the formation of excitatory synapses.
引用
收藏
页码:1294 / 1301
页数:8
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