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NMDARs in granule cells contribute to parallel fiber-Purkinje cell synaptic plasticity and motor learning

Research group De Zeeuw
Publication year 2021
Published in Proceedings of the National Academy of Sciences of the United States of America
Authors C.I. De Zeeuw, Martijn Schonewille, Allison E Girasole, Philippe Rostaing, Caroline Mailhes-Hamon, Annick Ayon, Alexandra B Nelson, Antoine Triller, Mariano Casado, Guy Bouvier,
The order of authors may deviate from the original publication due to temporary technical issues.

Long-term synaptic plasticity is believed to be the cellular substrate of learning and memory. Synaptic plasticity rules are defined by the specific complement of receptors at the synapse and the associated downstream signaling mechanisms. In young rodents, at the cerebellar synapse between granule cells (GC) and Purkinje cells (PC), bidirectional plasticity is shaped by the balance between transcellular nitric oxide (NO) driven by presynaptic N-methyl-D-aspartate receptor (NMDAR) activation and postsynaptic calcium dynamics. However, the role and the location of NMDAR activation in these pathways is still debated in mature animals. Here, we show in adult rodents that NMDARs are present and functional in presynaptic terminals where their activation triggers NO signaling. In addition, we find that selective genetic deletion of presynaptic, but not postsynaptic, NMDARs prevents synaptic plasticity at parallel fiber-PC (PF-PC) synapses. Consistent with this finding, the selective deletion of GC NMDARs affects adaptation of the vestibulo-ocular reflex. Thus, NMDARs presynaptic to PCs are required for bidirectional synaptic plasticity and cerebellar motor learning.

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