Ca.sup.2+ channel and active zone protein abundance intersects with input-specific synapse organization to shape functional synaptic diversity

• Published in: eLife Vol. 12
• Main Authors: Medeiros, Audrey T, Gratz, Scott J, Delgado, Ambar, Ritt, Jason T, O'Connor-Giles, Kate M
• Format: Journal Article
• Language: English
• Published: eLife Science Publications, Ltd 18-09-2024
• Subjects: Calcium channels; Glutamate; Neural circuitry; Neurophysiology; Canada
• ISSN: 2050-084X; 2050-084X
• DOI: 10.7554/eLife.88412

Synaptic heterogeneity is a hallmark of nervous systems that enables complex and adaptable communication in neural circuits. To understand circuit function, it is thus critical to determine the factors that contribute to the functional diversity of synapses. We investigated the contributions of voltage-gated calcium channel (VGCC) abundance, spatial organization, and subunit composition to synapse diversity among and between synapses formed by two closely related Drosophila glutamatergic motor neurons with distinct neurotransmitter release probabilities (P.sub.r). Surprisingly, VGCC levels are highly predictive of heterogeneous P.sub.r among individual synapses of either low- or high-P.sub.r inputs, but not between inputs. We find that the same number of VGCCs are more densely organized at high-P.sub.r synapses, consistent with tighter VGCC-synaptic vesicle coupling. We generated endogenously tagged lines to investigate VGCC subunits in vivo and found that the [alpha]2[delta]--3 subunit Straightjacket along with the CAST/ELKS active zone (AZ) protein Bruchpilot, both key regulators of VGCCs, are less abundant at high-P.sub.r inputs, yet positively correlate with P.sub.r among synapses formed by either input. Consistently, both Straightjacket and Bruchpilot levels are dynamically increased across AZs of both inputs when neurotransmitter release is potentiated to maintain stable communication following glutamate receptor inhibition. Together, these findings suggest a model in which VGCC and AZ protein abundance intersects with input-specific spatial and molecular organization to shape the functional diversity of synapses.