TY - JOUR
T1 - The ubiquitous nature of multivesicular release
AU - Rudolph, Stephanie
AU - Tsai, Ming Chi
AU - von Gersdorff, Henrique
AU - Wadiche, Jacques I.
N1 - Funding Information:
This work was supported by National Institutes of Health grants to J.I.W. (R01NS065920) and H.v.G. (R01DC012938 and R01DC04274). We thank Drs Monica Thanawala, Pascal Kaeser, Jessica Hauser, Anastasios Tzingounis, Jada Vaden, Linda Overstreet-Wadiche, and members of the laboratory of J.I.W. for reading the manuscript.
Publisher Copyright:
© 2015 Elsevier Ltd.
PY - 2015/7/1
Y1 - 2015/7/1
N2 - 'Simplicity is prerequisite for reliability' (E.W. Dijkstra [1]). Presynaptic action potentials trigger the fusion of vesicles to release neurotransmitter onto postsynaptic neurons. Each release site was originally thought to liberate at most one vesicle per action potential in a probabilistic fashion, rendering synaptic transmission unreliable. However, the simultaneous release of several vesicles, or multivesicular release (MVR), represents a simple mechanism to overcome the intrinsic unreliability of synaptic transmission. MVR was initially identified at specialized synapses but is now known to be common throughout the brain. MVR determines the temporal and spatial dispersion of transmitter, controls the extent of receptor activation, and contributes to adapting synaptic strength during plasticity and neuromodulation. MVR consequently represents a widespread mechanism that extends the dynamic range of synaptic processing.
AB - 'Simplicity is prerequisite for reliability' (E.W. Dijkstra [1]). Presynaptic action potentials trigger the fusion of vesicles to release neurotransmitter onto postsynaptic neurons. Each release site was originally thought to liberate at most one vesicle per action potential in a probabilistic fashion, rendering synaptic transmission unreliable. However, the simultaneous release of several vesicles, or multivesicular release (MVR), represents a simple mechanism to overcome the intrinsic unreliability of synaptic transmission. MVR was initially identified at specialized synapses but is now known to be common throughout the brain. MVR determines the temporal and spatial dispersion of transmitter, controls the extent of receptor activation, and contributes to adapting synaptic strength during plasticity and neuromodulation. MVR consequently represents a widespread mechanism that extends the dynamic range of synaptic processing.
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U2 - 10.1016/j.tins.2015.05.008
DO - 10.1016/j.tins.2015.05.008
M3 - Review article
C2 - 26100141
AN - SCOPUS:84933670336
SN - 0166-2236
VL - 38
SP - 428
EP - 438
JO - Trends in Neurosciences
JF - Trends in Neurosciences
IS - 7
ER -