SynCAM, a synaptic adhesion molecule that drives synapse assembly

被引:605
作者
Biederer, T
Sara, Y
Mozhayeva, M
Atasoy, D
Liu, XR
Kavalali, ET
Südhof, TC
机构
[1] Univ Texas, Ctr Basic Neurosci, SW Med Ctr, Dallas, TX 75390 USA
[2] Univ Texas, Dept Mol Genet, SW Med Ctr, Dallas, TX 75390 USA
[3] Univ Texas, Dept Physiol, SW Med Ctr, Dallas, TX 75390 USA
[4] Univ Texas, Howard Hughes Med Inst, SW Med Ctr, Dallas, TX 75390 USA
关键词
D O I
10.1126/science.1072356
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Synapses, the junctions between nerve cells through which they communicate, are formed by the coordinated assembly and tight attachment of pre- and postsynaptic specializations. We now show that SynCAM is a brain-specific, immunoglobulin domain containing protein that binds to intracellular PDZ-domain proteins and functions as a homophilic cell adhesion molecule at the synapse. Expression of the isolated cytoplasmic tail of SynCAM in neurons inhibited synapse assembly. Conversely, expression of full-length SynCAM in nonneuronal cells induced synapse formation by cocultured hippocampal neurons with normal release properties. Glutamatergic synaptic transmission was reconstituted in these nonneuronal cells by coexpressing glutamate receptors with SynCAM, which suggests that a single type of adhesion molecule and glutamate receptor are sufficient for a functional postsynaptic response.
引用
收藏
页码:1525 / 1531
页数:7
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