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Updated: Jan 26, 2026

An Optical Assay for Synaptic Vesicle Recycling in Cultured Neurons Overexpressing Presynaptic Proteins
Published on: June 26, 2018
Synaptic Vesicle Recycling Pathway Determines Neurotransmitter Content and Release Properties
Kätlin Silm1, Jing Yang1, Pamela F Marcott2
1Departments of Neurology and Physiology, Graduate Programs in Neuroscience and Cell Biology, Kavli Institute for Fundamental Neuroscience, Weill Institute for the Neurosciences, UCSF School of Medicine, San Francisco, CA 94143, USA.
Abstract:
In contrast to temporal coding by synaptically acting neurotransmitters such as glutamate, neuromodulators such as monoamines signal changes in firing rate. The two modes of signaling have been thought to reflect differences in release by different cells. We now find that midbrain dopamine neurons release glutamate and dopamine with different properties that reflect storage in different synaptic vesicles. The vesicles differ in release probability, coupling to presynaptic Ca2+ channels and frequency dependence. Although previous work has attributed variation in these properties to differences in location or cytoskeletal association of synaptic vesicles, the release of different transmitters shows that intrinsic differences in vesicle identity drive different modes of release. Indeed, dopamine but not glutamate vesicles depend on the adaptor protein AP-3, revealing an unrecognized linkage between the pathway of synaptic vesicle recycling and the properties of exocytosis. Storage of the two transmitters in different vesicles enables the transmission of distinct signals.
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