Modelling Vesicular Release at Hippocampal Synapses

Autor: Herbert Levine, Thomas M. Bartol, Suhita Nadkarni, Terrence J. Sejnowski
Jazyk: angličtina
Rok vydání: 2010
Předmět:
Biophysics/Theory and Simulation
Vesicle fusion
Refractory period
Models
Neurological

Computational Biology/Computational Neuroscience
Hippocampal formation
Neurotransmission
Synaptic vesicle
Synaptic Transmission
Exocytosis
Cell Biology/Cell Signaling
03 medical and health sciences
Cellular and Molecular Neuroscience
0302 clinical medicine
Genetics
Neuroscience/Neuronal Signaling Mechanisms
Biophysics/Cell Signaling and Trafficking Structures
Computer Simulation
Neuroscience/Theoretical Neuroscience
Molecular Biology
lcsh:QH301-705.5
CA1 Region
Hippocampal

Ecology
Evolution
Behavior and Systematics

Simulation
030304 developmental biology
0303 health sciences
Stochastic Processes
Neuronal Plasticity
Ecology
Voltage-dependent calcium channel
Chemistry
Vesicle
Neuroscience/Neuronal and Glial Cell Biology
Reproducibility of Results
CA3 Region
Hippocampal

Computational Biology/Signaling Networks
Computational Theory and Mathematics
lcsh:Biology (General)
Modeling and Simulation
Synapses
Biophysics
Biophysics/Biomacromolecule-Ligand Interactions
Calcium
Synaptic Vesicles
Monte Carlo Method
030217 neurology & neurosurgery
Research Article
Zdroj: PLoS Computational Biology
PLoS Computational Biology, Vol 6, Iss 11, p e1000983 (2010)
ISSN: 1553-7358
1553-734X
Popis: We study local calcium dynamics leading to a vesicle fusion in a stochastic, and spatially explicit, biophysical model of the CA3-CA1 presynaptic bouton. The kinetic model for vesicle release has two calcium sensors, a sensor for fast synchronous release that lasts a few tens of milliseconds and a separate sensor for slow asynchronous release that lasts a few hundred milliseconds. A wide range of data can be accounted for consistently only when a refractory period lasting a few milliseconds between releases is included. The inclusion of a second sensor for asynchronous release with a slow unbinding site, and thereby a long memory, affects short-term plasticity by facilitating release. Our simulations also reveal a third time scale of vesicle release that is correlated with the stimulus and is distinct from the fast and the slow releases. In these detailed Monte Carlo simulations all three time scales of vesicle release are insensitive to the spatial details of the synaptic ultrastructure. Furthermore, our simulations allow us to identify features of synaptic transmission that are universal and those that are modulated by structure.
Author Summary Chemical synaptic transmission in neurons takes place when a neurotransmitter released from a nerve terminal of the presynaptic neuron signals to the postsynaptic neuron that an event has occurred. The goal of our research was to model the release at a type of synapse found in the hippocampus, a part of the brain that is involved with learning and memory. The synapse model was simulated in a computer that kept track of all of the important molecules in the nerve terminal. The model led to a better understanding of the extant experimental data including exact conditions that lead to the release of a single packet of neurotransmitter. According to our model, the release of more than one packet can be triggered by a single presynaptic event but the packets are released one at a time. Furthermore, we uncovered the mechanisms underlying an extremely fast form of release that had not been previously studied. The model made predictions for other properties of the synapse that can be tested experimentally. A better understanding of how the normal synapses in the hippocampus work will help us to better understand what goes wrong with synapses in mental disorders such as depression and schizophrenia.
Databáze: OpenAIRE