A system of feed-forward cerebellar circuits that extend and diversify sensory signaling

Sensory signals are processed by the cerebellum to coordinate movements. Numerous cerebellar functions are thought to require the maintenance of a sensory representation that extends beyond the input signal. Granule cells receive sensory input, but they do not prolong the signal and are thus unlikely to maintain a sensory representation for much longer than the inputs themselves. Unipolar brush cells (UBCs) are excitatory interneurons that project to granule cells and transform sensory input into prolonged increases or decreases in firing, depending on their ON or OFF UBC subtype. Further extension and diversification of the input signal could be produced by UBCs that project to one another, but whether this circuitry exists is unclear. Here we test whether UBCs innervate one another and explore how these small networks of UBCs could transform spiking patterns. We characterized two transgenic mouse lines electrophysiologically and immunohistochemically to confirm that they label ON and OFF UBC subtypes and crossed them together, revealing that ON and OFF UBCs innervate one another. A Brainbow reporter was used to label UBCs of the same ON or OFF subtype with different fluorescent proteins, which showed that UBCs innervate their own subtypes as well. Computational models predict that these feed-forward networks of UBCs extend the length of bursts or pauses and introduce delays—transformations that may be necessary for cerebellar functions from modulation of eye movements to adaptive learning across time scales. SIGNIFICANCE STATEMENT The cerebellum is essential for the accurate performance of behaviors ranging in complexity from stabilizing an image on the retina to playing a piano or performing a gymnastics routine. Cerebellar dysfunction disrupts the ability to produce smooth movements and leads to a disorder called ataxia. Damage to the vestibular cerebellum occurs in various disorders including medulloblastoma and leads to nystagmus, involuntary movements of the eyes that prevent normal vision. Treating disorders of motor control such as nystagmus, requires a better understanding of how representations of movements are maintained in the firing patterns of neurons in the cerebellar circuit. Here we use transgenic mice to label a type of neuron called the unipolar brush cell and revealed that these cells innervate one another and are likely to increase the length and diversity of spiking patterns in the cerebellum. These transformations may be necessary for numerous functions from controlling eye movements to learning new behaviors.

[1]  L. Trussell,et al.  Descending Axonal Projections from the Inferior Colliculus Target Nearly All Excitatory and Inhibitory Cell Types of the Dorsal Cochlear Nucleus , 2022, The Journal of Neuroscience.

[2]  Evan Z. Macosko,et al.  A transcriptomic atlas of mouse cerebellar cortex comprehensively defines cell types , 2021, Nature.

[3]  Evan Z. Macosko,et al.  Peer Review File Manuscript Title: A transcriptomic atlas of mouse cerebellar cortex reveals novel cell types Editorial Notes: Reviewer Comments & Author Rebuttals , 2020 .

[4]  L. Trussell,et al.  Trigeminal Contributions to the Dorsal Cochlear Nucleus in Mouse , 2021, Frontiers in Neuroscience.

[5]  Evan Z. Macosko,et al.  Graded heterogeneity of metabotropic signaling underlies a continuum of cell-intrinsic temporal responses in unipolar brush cells , 2020, Nature Communications.

[6]  Carolina Borges-Merjane,et al.  Incomplete removal of extracellular glutamate controls synaptic transmission and integration at a cerebellar synapse , 2020, bioRxiv.

[7]  Aparna Suvrathan,et al.  Beyond STDP—towards diverse and functionally relevant plasticity rules , 2019, Current Opinion in Neurobiology.

[8]  L. Trussell,et al.  Selective targeting of unipolar brush cell subtypes by cerebellar mossy fibers , 2019, bioRxiv.

[9]  L. Trussell,et al.  Slow AMPAR Synaptic Transmission Is Determined by Stargazin and Glutamate Transporters , 2017, Neuron.

[10]  B. Cohen,et al.  Coding of Velocity Storage in the Vestibular Nuclei , 2017, Front. Neurol..

[11]  Jian K. Liu,et al.  Mechanisms and functional roles of glutamatergic synapse diversity in a cerebellar circuit , 2016, eLife.

[12]  Ken Sugino,et al.  A Mammalian enhancer trap resource for discovering and manipulating neuronal cell types , 2016, eLife.

[13]  R. A. Hensbroek,et al.  Visuo-Vestibular Information Processing by Unipolar Brush Cells in the Rabbit Flocculus , 2015, The Cerebellum.

[14]  C. I. Zeeuw,et al.  Forward Signaling by Unipolar Brush Cells in the Mouse Cerebellum , 2015, The Cerebellum.

[15]  Richard J. Edwards,et al.  Metabotropic Glutamate Receptors , 2015, The Journal of Biological Chemistry.

[16]  Egidio D'Angelo,et al.  Computational modeling predicts the ionic mechanism of late-onset responses in unipolar brush cells , 2014, Front. Cell. Neurosci..

[17]  C. D. De Zeeuw,et al.  Variable timing of synaptic transmission in cerebellar unipolar brush cells , 2014, Proceedings of the National Academy of Sciences.

[18]  Masahiko Watanabe,et al.  Differential distribution of phospholipase C beta isoforms and diaglycerol kinase-beta in rodents cerebella corroborates the division of unipolar brush cells into two major subtypes , 2014, Brain Structure and Function.

[19]  Greg Wayne,et al.  A temporal basis for predicting the sensory consequences of motor commands in an electric fish , 2014, Nature Neuroscience.

[20]  C. Gerfen,et al.  GENSAT BAC Cre-Recombinase Driver Lines to Study the Functional Organization of Cerebral Cortical and Basal Ganglia Circuits , 2013, Neuron.

[21]  E. D’Angelo,et al.  Late‐onset bursts evoked by mossy fibre bundle stimulation in unipolar brush cells: evidence for the involvement of H‐ and TRP‐currents , 2013, The Journal of physiology.

[22]  Josef Spacek,et al.  Extracellular sheets and tunnels modulate glutamate diffusion in hippocampal neuropil , 2013, The Journal of comparative neurology.

[23]  E. Mugnaini,et al.  Electrophysiological, Morphological, and Topological Properties of Two Histochemically Distinct Subpopulations of Cerebellar Unipolar Brush Cells , 2012, The Cerebellum.

[24]  S. Nelson,et al.  A Resource of Cre Driver Lines for Genetic Targeting of GABAergic Neurons in Cerebral Cortex , 2011, Neuron.

[25]  Enrico Mugnaini,et al.  The unipolar brush cell: A remarkable neuron finally receiving deserved attention , 2011, Brain Research Reviews.

[26]  Hans Clevers,et al.  Intestinal Crypt Homeostasis Results from Neutral Competition between Symmetrically Dividing Lgr5 Stem Cells , 2010, Cell.

[27]  Allan R. Jones,et al.  A robust and high-throughput Cre reporting and characterization system for the whole mouse brain , 2009, Nature Neuroscience.

[28]  Lokeshvar Nath Kalia,et al.  Timing and plasticity in the cerebellum: focus on the granular layer , 2009, Trends in Neurosciences.

[29]  R. W. Draft,et al.  Transgenic strategies for combinatorial expression of fluorescent proteins in the nervous system , 2007, Nature.

[30]  E. Mugnaini,et al.  Vesicular glutamate transporters VGLUT1 and VGLUT2 define two subsets of unipolar brush cells in organotypic cultures of mouse vestibulocerebellum , 2003, Neuroscience.

[31]  C. Haenggeli,et al.  Multimodal inputs to the granule cell domain of the cochlear nucleus , 2003, Experimental Brain Research.

[32]  R. Shigemoto,et al.  Differential expression of calretinin and metabotropic glutamate receptor mGluR1α defines subsets of unipolar brush cells in mouse cerebellum , 2002, The Journal of comparative neurology.

[33]  S. Hooper,et al.  A computational role for slow conductances: single-neuron models that measure duration , 2002, Nature Neuroscience.

[34]  N. Slater,et al.  Unipolar brush cells form a glutamatergic projection system within the mouse cerebellar cortex , 2001, The Journal of comparative neurology.

[35]  N. Slater,et al.  Unipolar brush cell: a potential feedforward excitatory interneuron of the cerebellum , 2000, Neuroscience.

[36]  E. Mugnaini,et al.  Unipolar brush cell axons form a large system of intrinsic mossy fibers in the postnatal vestibulocerebellum , 2000, The Journal of comparative neurology.

[37]  S. Lisberger,et al.  Neural Learning Rules for the Vestibulo-Ocular Reflex , 1998, The Journal of Neuroscience.

[38]  Nicholas T. Carnevale,et al.  The NEURON Simulation Environment , 1997, Neural Computation.

[39]  D. Rossi,et al.  Properties of transmission at a giant glutamatergic synapse in cerebellum: the mossy fiber-unipolar brush cell synapse. , 1995, Journal of neurophysiology.

[40]  T. Sejnowski,et al.  A model of spindle rhythmicity in the isolated thalamic reticular nucleus. , 1994, Journal of neurophysiology.

[41]  E. Mugnaini,et al.  Extraordinary synapses of the unipolar brush cell: An electron microscopic study in the rat cerebellum , 1994, Synapse.

[42]  H. Axelrad,et al.  Granular layer collaterals of the unipolar brush cell axon display rosette-like excrescences. A Golgi study in the rat cerebellar cortex , 1994, Neuroscience Letters.

[43]  A G Barto,et al.  Toward a modern theory of adaptive networks: expectation and prediction. , 1981, Psychological review.

[44]  B. Cohen,et al.  Velocity storage in the vestibulo-ocular reflex arc (VOR) , 1979, Experimental Brain Research.

[45]  J. Goldberg,et al.  Physiology of peripheral neurons innervating semicircular canals of the squirrel monkey. II. Response to sinusoidal stimulation and dynamics of peripheral vestibular system. , 1971, Journal of neurophysiology.

[46]  D. Marr A theory of cerebellar cortex , 1969, The Journal of physiology.

[47]  J. Skangiel-Kramska,et al.  Vesicular glutamate transporters VGLUT1 and VGLUT2 in development of mouse barrel cortex , 2006 .

[48]  H. C. Hulscher,et al.  Between in and out: linking morphology and physiology of cerebellar cortical interneurons. , 2005, Progress in brain research.

[49]  O. Castejón Unipolar Brush Cells , 2003 .

[50]  R. Shigemoto,et al.  Metabotropic glutamate receptors are associated with non-synaptic appendages of unipolar brush cells in rat cerebellar cortex and cochlear nuclear complex , 1998, Journal of neurocytology.

[51]  A. Destexhe Kinetic Models of Synaptic Transmission , 1997 .

[52]  M. Ito Cerebellar control of the vestibulo-ocular reflex--around the flocculus hypothesis. , 1982, Annual review of neuroscience.