α-Latrotoxin and its receptors:: Neurexins and Cirl/latrophilins

alpha -Latrotoxin, a potent neurotoxin from black widow spider venom, triggers synaptic vesicle exocytosis from presynaptic nerve terminals. alpha -Latrotoxin is a large protein toxin (120 kDa) that contains 22 ankyrin repeats. In stimulating exocytosis, alpha -latrotoxin binds to two distinct families of neuronal cell-surface receptors, neurexins and CLs (Cir1/latrophilins), which probably have a physiological function in synaptic cell adhesion. Binding of alpha -latrotoxin to these receptors does not in itself trigger exocytosis but serves to recruit the toxin to the synapse. Receptor-bound alpha -latrotoxin then inserts into the presynaptic plasma membrane to stimulate exocytosis by two distinct transmitter-specific mechanisms. Exocytosis of classical neurotransmitters (glutamate, GABA, acetylcholine) is induced in a calcium-independent manner by a direct intracellular action of alpha -latrotoxin, while exocytosis of catecholamines requires extracellular calcium. Elucidation of precisely how alpha -latrotoxin works is likely to provide major insight into how synaptic vesicle exocytosis is regulated, and how the release machineries of classical and catecholaminergic neurotransmitters differ.