TY - JOUR
T1 - Implications of all-or-none synaptic transmission and short-term depression beyond vesicle depletion
T2 - A computational study
AU - Matveev, Victor
AU - Wang, Xiao Jing
PY - 2000/2/15
Y1 - 2000/2/15
N2 - The all-or-none character of transmission at central synapses is commonly viewed as evidence that only one vesicle can be released per action potential at a single release site. This interpretation is still a matter of debate; its resolution is important for our understanding of the nature of quantal response. In this work we explore observable consequences of the univesicular release hypothesis by studying a stochastic model of synaptic transmission. We investigated several alternative mechanisms for the all-or- none response: (1) the univesicular release constraint realized through lateral inhibition across presynaptic membrane, (2) the constraint of a single releasable vesicle per active zone, and (3) the postsynaptic receptor saturation. We show that both the univesicular release constraint and the postsynaptic receptor saturation lead to a limited amount of depression by vesicle depletion, so that depletion alone cannot account for the strong paired-pulse depression observed at some cortical synapses. Although depression can be rapid if there is only one releasable vesicle per active zone, this scenario leads to a limit on the transmission probability. We evaluate additional mechanisms beyond vesicle depletion, and our results suggest that the strong paired-pulse depression may be a result of activity- dependent inactivation of the exocytosis machinery. Furthermore, we found that the statistical analysis of release events, in response to a long stimulus train, might allow one to distinguish experimentally between univesicular and multivesicular release scenarios. We show that without the univesicular release constraint, the temporal correlation between release events is always negative, whereas it is typically positive with such a constraint if the vesicle fusion probability is sufficiently large.
AB - The all-or-none character of transmission at central synapses is commonly viewed as evidence that only one vesicle can be released per action potential at a single release site. This interpretation is still a matter of debate; its resolution is important for our understanding of the nature of quantal response. In this work we explore observable consequences of the univesicular release hypothesis by studying a stochastic model of synaptic transmission. We investigated several alternative mechanisms for the all-or- none response: (1) the univesicular release constraint realized through lateral inhibition across presynaptic membrane, (2) the constraint of a single releasable vesicle per active zone, and (3) the postsynaptic receptor saturation. We show that both the univesicular release constraint and the postsynaptic receptor saturation lead to a limited amount of depression by vesicle depletion, so that depletion alone cannot account for the strong paired-pulse depression observed at some cortical synapses. Although depression can be rapid if there is only one releasable vesicle per active zone, this scenario leads to a limit on the transmission probability. We evaluate additional mechanisms beyond vesicle depletion, and our results suggest that the strong paired-pulse depression may be a result of activity- dependent inactivation of the exocytosis machinery. Furthermore, we found that the statistical analysis of release events, in response to a long stimulus train, might allow one to distinguish experimentally between univesicular and multivesicular release scenarios. We show that without the univesicular release constraint, the temporal correlation between release events is always negative, whereas it is typically positive with such a constraint if the vesicle fusion probability is sufficiently large.
KW - Central synapse
KW - Exocytosis
KW - Receptor saturation
KW - Short-term depression
KW - Stochastic model
KW - Univesicular release
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U2 - 10.1523/jneurosci.20-04-01575.2000
DO - 10.1523/jneurosci.20-04-01575.2000
M3 - Article
C2 - 10662847
AN - SCOPUS:0034652344
SN - 0270-6474
VL - 20
SP - 1575
EP - 1588
JO - Journal of Neuroscience
JF - Journal of Neuroscience
IS - 4
ER -