Not only the amplitude but also the time course of a presynaptic Ca transient determine multiple aspects of synaptic transmission. In small bouton-type synapses, the mechanisms underlying the Ca decay kinetics have not been fully investigated. Here, factors that shape an action-potential-evoked Ca transient were quantitatively studied in synaptic boutons of neocortical layer 5 pyramidal neurons. Ca transients were measured with different concentrations of fluorescent Ca indicators and analyzed based on a single-compartment model. We found a small endogenous Ca-binding ratio (7 ± 2) and a high activity of Ca transporters (0.64 ± 0.03 ms), both of which enable rapid clearance of Ca from the boutons. However, contrary to predictions of the single-compartment model, the decay time course of the measured Ca transients was biexponential and became prolonged during repetitive stimulation. Measurements of [Ca] along the adjoining axon, together with an experimentally constrained model, showed that the initial fast decay of the Ca transients predominantly arose from the diffusion of Ca from the boutons into the axon. Therefore, for small boutons en passant, factors like terminal volume, axon diameter, and the concentration of mobile Ca-binding molecules are critical determinants of Ca dynamics and thus Ca-dependent processes, including short-term synaptic plasticity.
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http://dx.doi.org/10.1016/j.bpj.2018.07.018 | DOI Listing |
Methods Mol Biol
January 2025
Department of Biochemistry, Weill Cornell Medicine, New York, NY, USA.
Complexins are a family of small presynaptic proteins that regulate neurotransmitter release at nerve terminals and are highly conserved in evolution. While direct interactions with SNARE proteins are critical for all complexin functions, binding of their disordered C-terminal domains (CTD) to membranes, especially to synaptic vesicle membranes, is essential for the ability of complexin to inhibit vesicle release. Furthermore, while some complexin CTDs possess an endogenous affinity for membranes, other complexin isoforms are subject to lipidation at their C-termini, which is presumed to confer additional membrane binding.
View Article and Find Full Text PDFNPJ Parkinsons Dis
January 2025
Interfaculty Institute of Biochemistry, University of Tübingen, Tübingen, Germany.
The dysfunction of dopaminergic (DA) neurons is central to Parkinson's disease. Distinct synaptic vesicle (SV) populations, differing in neurotransmitter content (dopamine vs. glutamate), may vary due to differences in trafficking and exocytosis.
View Article and Find Full Text PDFNat Commun
December 2024
Nanobiology Institute, Yale University, West Haven, CT, USA.
Neurotransmitters are released from synaptic vesicles with remarkable precision in response to presynaptic calcium influx but exhibit significant heterogeneity in exocytosis timing and efficacy based on the recent history of activity. This heterogeneity is critical for information transfer in the brain, yet its molecular basis remains poorly understood. Here, we employ a biochemically-defined fusion assay under physiologically relevant conditions to delineate the minimal protein machinery sufficient to account for various modes of calcium-triggered vesicle fusion dynamics.
View Article and Find Full Text PDFHippocampus
January 2025
Departments of Child & Adolescent Psychiatry, Neuroscience & Physiology, and Psychiatry, and the Neuroscience Institute, New York University Langone Health, New York, New York, USA.
Active conductances tune the kinetics of axonal action potentials (APs) to support specialized functions of neuron types. However, the temporal characteristics of voltage signals strongly depend on the size of neuronal structures, as capacitive and resistive effects slow down voltage discharges in the membranes of small elements. Axonal action potentials are particularly sensitive to these inherent biophysical effects because of the large diameter variabilities within individual axons, potentially implying bouton size-dependent synaptic effects.
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