Neuromodulator signaling bidirectionally controls vesicle numbers in human synapses

Neuromodulators bind to pre- and postsynaptic G protein-coupled receptors (GPCRs), are able to quickly change intracellular cyclic AMP (cAMP) and Ca2+ levels, and are thought to play important roles in neuropsychiatric and neurodegenerative diseases. Here, we discovered in human neurons an unanticip...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: Patzke, Christopher (VerfasserIn) , Acuna Goycolea, Claudio (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 3 October 2019
In: Cell
Year: 2019, Jahrgang: 179, Heft: 2, Pages: 498-513.e22
ISSN:1097-4172
DOI:10.1016/j.cell.2019.09.011
Online-Zugang:Verlag, Volltext: https://doi.org/10.1016/j.cell.2019.09.011
Verlag: http://www.sciencedirect.com/science/article/pii/S0092867419310177
Volltext
Verfasserangaben:Christopher Patzke, Marisa M. Brockmann, Jinye Dai, Kathlyn J. Gan, M. Katharina Grauel, Pascal Fenske, Yu Liu, Claudio Acuna, Christian Rosenmund, and Thomas C. Südhof
Beschreibung
Zusammenfassung:Neuromodulators bind to pre- and postsynaptic G protein-coupled receptors (GPCRs), are able to quickly change intracellular cyclic AMP (cAMP) and Ca2+ levels, and are thought to play important roles in neuropsychiatric and neurodegenerative diseases. Here, we discovered in human neurons an unanticipated presynaptic mechanism that acutely changes synaptic ultrastructure and regulates synaptic communication. Activation of neuromodulator receptors bidirectionally controlled synaptic vesicle numbers within nerve terminals. This control correlated with changes in the levels of cAMP-dependent protein kinase A-mediated phosphorylation of synapsin-1. Using a conditional deletion approach, we reveal that the neuromodulator-induced control of synaptic vesicle numbers was largely dependent on synapsin-1. We propose a mechanism whereby non-phosphorylated synapsin-1 “latches” synaptic vesicles to presynaptic clusters at the active zone. cAMP-dependent phosphorylation of synapsin-1 then removes the vesicles. cAMP-independent dephosphorylation of synapsin-1 in turn recruits vesicles. Synapsin-1 thereby bidirectionally regulates synaptic vesicle numbers and modifies presynaptic neurotransmitter release as an effector of neuromodulator signaling in human neurons.
Beschreibung:Gesehen am 25.10.2019
Beschreibung:Online Resource
ISSN:1097-4172
DOI:10.1016/j.cell.2019.09.011