Presynaptic cGMP sets synaptic strength in the striatum and is important for motor learning
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Presynaptic cGMP sets synaptic strength in the striatum and is important for motor learning. / Fieblinger, Tim; Perez-Alvarez, Alberto; Lamothe-Molina, Paul J; Gee, Christine E; Oertner, Thomas G.
in: EMBO REP, Jahrgang 23, Nr. 8, e54361, 03.08.2022.Publikationen: SCORING: Beitrag in Fachzeitschrift/Zeitung › SCORING: Zeitschriftenaufsatz › Forschung › Begutachtung
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TY - JOUR
T1 - Presynaptic cGMP sets synaptic strength in the striatum and is important for motor learning
AU - Fieblinger, Tim
AU - Perez-Alvarez, Alberto
AU - Lamothe-Molina, Paul J
AU - Gee, Christine E
AU - Oertner, Thomas G
N1 - © 2022 The Authors. Published under the terms of the CC BY 4.0 license.
PY - 2022/8/3
Y1 - 2022/8/3
N2 - The striatum is a subcortical brain region responsible for the initiation and termination of voluntary movements. Striatal spiny projection neurons receive major excitatory synaptic input from neocortex and thalamus, and cyclic nucleotides have long been known to play important roles in striatal function. Yet, the precise mechanism of action is unclear. Here, we combine optogenetic stimulation, 2-photon imaging, and genetically encoded scavengers to dissect the regulation of striatal synapses in mice. Our data show that excitatory striatal inputs are tonically depressed by phosphodiesterases (PDEs), in particular PDE1. Blocking PDE activity boosts presynaptic calcium entry and glutamate release, leading to strongly increased synaptic transmission. Although PDE1 degrades both cAMP and cGMP, we uncover that the concentration of cGMP, not cAMP, controls the gain of striatal inputs. Disturbing this gain control mechanism in vivo impairs motor skill learning in mice. The tight dependence of striatal excitatory synapses on PDE1 and cGMP offers a new perspective on the molecular mechanisms regulating striatal activity.
AB - The striatum is a subcortical brain region responsible for the initiation and termination of voluntary movements. Striatal spiny projection neurons receive major excitatory synaptic input from neocortex and thalamus, and cyclic nucleotides have long been known to play important roles in striatal function. Yet, the precise mechanism of action is unclear. Here, we combine optogenetic stimulation, 2-photon imaging, and genetically encoded scavengers to dissect the regulation of striatal synapses in mice. Our data show that excitatory striatal inputs are tonically depressed by phosphodiesterases (PDEs), in particular PDE1. Blocking PDE activity boosts presynaptic calcium entry and glutamate release, leading to strongly increased synaptic transmission. Although PDE1 degrades both cAMP and cGMP, we uncover that the concentration of cGMP, not cAMP, controls the gain of striatal inputs. Disturbing this gain control mechanism in vivo impairs motor skill learning in mice. The tight dependence of striatal excitatory synapses on PDE1 and cGMP offers a new perspective on the molecular mechanisms regulating striatal activity.
U2 - 10.15252/embr.202154361
DO - 10.15252/embr.202154361
M3 - SCORING: Journal article
C2 - 35735260
VL - 23
JO - EMBO REP
JF - EMBO REP
SN - 1469-221X
IS - 8
M1 - e54361
ER -