RIM Determines Ca2+ Channel Density and Vesicle Docking at the Presynaptic Active Zone

SummaryAt presynaptic active zones, neurotransmitter release is initiated by the opening of voltage-gated Ca2+ channels close to docked vesicles. The mechanisms that enrich Ca2+ channels at active zones are, however, largely unknown, possibly because of the limited presynaptic accessibility of most synapses. Here, we have established a Cre-lox based conditional knockout approach at a presynaptically accessible central nervous system synapse, the calyx of Held, to directly study the functions of RIM proteins. Removal of all RIM1/2 isoforms strongly reduced the presynaptic Ca2+ channel density, revealing a role of RIM proteins in Ca2+ channel targeting. Removal of RIMs also reduced the readily releasable pool, paralleled by a similar reduction of the number of docked vesicles, and the Ca2+ channel-vesicle coupling was decreased. Thus, RIM proteins co-ordinately regulate key functions for fast transmitter release, enabling a high presynaptic Ca2+ channel density and vesicle docking at the active zone.

► A conditional knockout approach for the calyx of Held synapse
► Presynaptic recording shows that RIM proteins enrich Ca2+ channels at the active zone
► RIM1/2 proteins determine the number of docked and readily releasable vesicles
► RIM1/2 proteins coordinate vesicle docking and Ca2+ channel density at the synapse