Mechanisms and functional roles of glutamatergic synapse diversity in a cerebellar circuit
Valeria Zampini,
Jian K Liu,
Marco A Diana,
Paloma P Maldonado,
Nicolas Brunel,
Stéphane Dieudonné
Affiliations
Valeria Zampini
Institut de Biologie de l'ENS, Ecole Normale Supérieure, Paris, France; Inserm, U1024, Paris, France; CNRS, UMR 8197, Paris, France
Jian K Liu
Neurosciences Federation, Université Paris Descartes, Paris, France; Department of Ophthalmology, University Medical Center Goettingen, Goettingen, Germany; Bernstein Center for Computational Neuroscience, Göttingen, Germany
Marco A Diana
Institut de Biologie de l'ENS, Ecole Normale Supérieure, Paris, France; Inserm, U1024, Paris, France; CNRS, UMR 8197, Paris, France
Paloma P Maldonado
Institut de Biologie de l'ENS, Ecole Normale Supérieure, Paris, France; Inserm, U1024, Paris, France; CNRS, UMR 8197, Paris, France
Neurosciences Federation, Université Paris Descartes, Paris, France; Department of Statistics and Neurobiology, University of Chicago, Chicago, United States
Stéphane Dieudonné
Institut de Biologie de l'ENS, Ecole Normale Supérieure, Paris, France; Inserm, U1024, Paris, France; CNRS, UMR 8197, Paris, France
Synaptic currents display a large degree of heterogeneity of their temporal characteristics, but the functional role of such heterogeneities remains unknown. We investigated in rat cerebellar slices synaptic currents in Unipolar Brush Cells (UBCs), which generate intrinsic mossy fibers relaying vestibular inputs to the cerebellar cortex. We show that UBCs respond to sinusoidal modulations of their sensory input with heterogeneous amplitudes and phase shifts. Experiments and modeling indicate that this variability results both from the kinetics of synaptic glutamate transients and from the diversity of postsynaptic receptors. While phase inversion is produced by an mGluR2-activated outward conductance in OFF-UBCs, the phase delay of ON UBCs is caused by a late rebound current resulting from AMPAR recovery from desensitization. Granular layer network modeling indicates that phase dispersion of UBC responses generates diverse phase coding in the granule cell population, allowing climbing-fiber-driven Purkinje cell learning at arbitrary phases of the vestibular input.