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Release probability of hippocampal glutamatergic terminals scales with the size of the active zone

Cortical synapses display remarkable structural, molecular and functional heterogeneity. Our knowledge regarding the relationship between the ultrastructural and functional parameters is still fragmented. Here we asked how the release probability and presynaptic [Ca(2+)] transients relate to the ult...

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Detalles Bibliográficos
Autores principales: Holderith, Noemi, Lorincz, Andrea, Katona, Gergely, Rózsa, Balázs, Kulik, Akos, Watanabe, Masahiko, Nusser, Zoltan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3386897/
https://www.ncbi.nlm.nih.gov/pubmed/22683683
http://dx.doi.org/10.1038/nn.3137
Descripción
Sumario:Cortical synapses display remarkable structural, molecular and functional heterogeneity. Our knowledge regarding the relationship between the ultrastructural and functional parameters is still fragmented. Here we asked how the release probability and presynaptic [Ca(2+)] transients relate to the ultrastructure of rat hippocampal glutamatergic axon terminals. Two-photon Ca(2+) imaging-derived optical quantal analysis and correlated electron microscopic reconstructions revealed a tight correlation between the release probability and the active zone area. The peak amplitude of [Ca(2+)] transients in single boutons also positively correlated with the active zone area. Freeze-fracture immunogold labeling revealed that the voltage-gated Ca(2+) channel subunit Cav2.1 and the presynaptic protein Rim1/2 are confined to the active zone and their numbers scale linearly with the active zone area. Gold particles for Cav2.1 showed a nonrandom distribution within the active zones. Our results demonstrate that the number of several active zone proteins, including presynaptic Ca(2+) channels, docked vesicles and the release probability scales linearly with the active zone area.