Complexins regulate a late step in Ca2+-dependent neurotransmitter release.

Journal:

Cell 2001 Jan

Authors:

Reim K, Mansour M, Varoqueaux F, McMahon HT, Südhof TC, Brose N, Rosenmund C

Abstract

Synaptic vesicle fusion at synapses is triggered by increases in cytosolic Ca2+ levels. However, the identity of the Ca2+ sensor and the transduction mechanism of the Ca2+ trigger are unknown. We show that Complexins, stoichiometric components of the exocytotic core complex, are important regulators of transmitter release at a step immediately preceding vesicle fusion. Neurons lacking Complexins show a dramatically reduced transmitter release efficiency due to decreased Ca2+ sensitivity of the s
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ynaptic secretion process. Analyses of mutant neurons demonstrate that Complexins are acting at or following the Ca2+-triggering step of fast synchronous transmitter release by regulating the exocytotic Ca2+ sensor, its interaction with the core complex fusion machinery, or the efficiency of the fusion apparatus itself.[less]

Mesh Headings:

Adaptor Proteins, Vesicular Transport, Animals, Calcimycin, Calcium, Cells, Cultured, Excitatory Postsynaptic Potentials, Gene Deletion, Hippocampus, Ionophores, Mice, Mice, Mutant Strains, Microscopy, Electron, Nerve Tissue Proteins, Neuronal Plasticity, Neurons, Neurotransmitter Agents, Patch-Clamp Techniques, Synaptic Transmission, Synaptic Vesicles