Neurexins are functional α-latrotoxin receptors

被引:80
作者
Sugita, S
Khvochtev, M
Südhof, TC
机构
[1] Univ Texas, SW Med Ctr, Howard Hughes Med Inst, Ctr Basic Neurosci, Dallas, TX 75235 USA
[2] Univ Texas, SW Med Ctr, Howard Hughes Med Inst, Dept Mol Genet, Dallas, TX 75235 USA
关键词
D O I
10.1016/S0896-6273(00)80704-7
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
alpha-Latrotoxin is a potent neurotoxin that triggers synaptic exocytosis. Surprisingly, two distinct neuronal receptors for alpha-latrotoxin have been described: CIRL/latrophilin 1 (CL1) and neurexin-1 alpha, alpha-latrotoxin is thought to trigger exocytosis by binding to CL1,while the role of neurexin 1 alpha is uncertain. Using PC12 cells, we now demonstrate that neurexins indeed function as alpha-latrotoxin receptors that are at least as potent as CL1. Both alpha- and beta-neurexins represent autonomous alpha latrotoxin receptors that are regulated by alternative splicing. Similar to CL1, truncated neurexins without intracellular sequences are fully active; therefore, neurexins and CL1 recruit alpha-latrotoxin but are not themselves involved in exocytosis. Thus, alpha-latrotoxin is unique among neurotoxins, because it utilizes two unrelated receptors, probably to amplify recruitment of alpha-latrotoxin to active sites.
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页码:489 / 496
页数:8
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