scholarly journals Resolving the Ultrastructural Organization of Synaptic Vesicle Pools at Hippocampal Mossy Fiber and Schaffer Collateral Synapses

2021 ◽  
Author(s):  
Maus Lydia Susann
2019 ◽  
Author(s):  
Lydia Maus ◽  
Bekir Altas ◽  
JeongSeop Rhee ◽  
Nils Brose ◽  
Cordelia Imig ◽  
...  

SUMMARYDespite similarities in the composition of the molecular release machinery, synapses can exhibit strikingly different functional transmitter release properties and short- and long-term plasticity characteristics. To address the question whether ultrastructural differences could contribute to this functional synaptic heterogeneity, we employed a combination of hippocampal organotypic slice cultures, high-pressure freezing, freeze substitution, and 3D-electron tomography to resolve the spatial organization of vesicle pools at individual active zones (AZ) in two functionally distinct synapses, namely Schaffer collateral (SC) and mossy fiber (MF) synapses. We found that mature MF and SC synapses harbor equal numbers of docked vesicles at their AZs, MF synapses at rest exhibit a second pool of possibly ‘tethered’ vesicles in the AZ vicinity, and MF synapses contain at least three morphological types of docked vesicles, indicating that differences in the ultrastructural organization of MF and SC synapses may contribute to their respective functional properties and corresponding plasticity characteristics.


2005 ◽  
Vol 51 (4) ◽  
pp. 435-443 ◽  
Author(s):  
Susumu Kumashiro ◽  
Yun-Fei Lu ◽  
Kazuhito Tomizawa ◽  
Masayuki Matsushita ◽  
Fan-Yan Wei ◽  
...  

2020 ◽  
Author(s):  
Camila Pulido ◽  
Timothy Aidan Ryan

The human brain is a uniquely vulnerable organ as interruption in fuel supply leads to acute cognitive impairment on rapid time scales. The reasons for this vulnerability are not well understood, but nerve terminals are likely loci of this vulnerability as they do not store sufficient ATP molecules and must synthesize them on-demand during activity or suffer acute degradation in performance. The requirements for on-demand ATP synthesis however depends in part on the magnitude of resting metabolic rates. We show here that, at rest, synaptic vesicle (SV) pools are a major source of presynaptic basal energy consumption. This basal metabolism arises from SV-resident V-ATPases compensating for a hidden resting H+ efflux from the SV lumen. We show that this steady-state H+ efflux is 1) mediated by vesicular neurotransmitter transporters, 2) independent of the SV cycle, 3) accounts for ~half of the resting synaptic energy consumption and 4) contributes to nerve terminal intolerance of fuel deprivation.


2001 ◽  
Vol 21 (12) ◽  
pp. 4195-4206 ◽  
Author(s):  
Yann Humeau ◽  
Frédéric Doussau ◽  
Francesco Vitiello ◽  
Paul Greengard ◽  
Fabio Benfenati ◽  
...  

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