Literature DB >> 17804630

Molecular, topographic, and functional organization of the cerebellar nuclei: analysis by three-dimensional mapping of the olivonuclear projection and aldolase C labeling.

Izumi Sugihara1, Yoshikazu Shinoda.   

Abstract

The olivocerebellar climbing fiber projection pattern is closely correlated with the pattern of aldolase C expression in cerebellar Purkinje cells. Based on this expression pattern, the olivocerebellar projection can be classified into five "groups" of functional compartments. Each group originates from a subarea within the inferior olive that projects to multiple cortical stripes of Purkinje cells, all of which are either aldolase C positive or aldolase C negative. However, no equivalent compartmental organization has been demonstrated in the cerebellar nuclei (CN). Thus, in the CN of the rat, we systematically mapped the location of olivonuclear projections belonging to the five groups and determined their relationship to the expression of aldolase C in Purkinje cell axonal terminals. The CN were divided into caudoventral aldolase C-positive and rostrodorsal aldolase C-negative parts. The olivonuclear terminations from the five groups projected topographically to five separate compartments within the CN that partly crossed the traditional boundaries that define the fastigial, interposed, and dentate nuclei. Each compartment had mostly uniform cytoarchitecture and the same aldolase C expression (either positive or negative) that was found in the corresponding olivocortical projection. These results suggest a new view of the organization of the CN whereby the pattern of olivonuclear terminations links portions of different CN together. We propose that each compartment in the CN, along with its corresponding olivary subarea and cortical stripes, may be related to a different aspect of motor control.

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Year:  2007        PMID: 17804630      PMCID: PMC6672958          DOI: 10.1523/JNEUROSCI.1579-07.2007

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.167


  39 in total

Review 1.  Compartmentalization of the deep cerebellar nuclei based on afferent projections and aldolase C expression.

Authors:  Izumi Sugihara
Journal:  Cerebellum       Date:  2011-09       Impact factor: 3.847

Review 2.  Motor Learning and the Cerebellum.

Authors:  Chris I De Zeeuw; Michiel M Ten Brinke
Journal:  Cold Spring Harb Perspect Biol       Date:  2015-09-01       Impact factor: 10.005

3.  Complex spike synchrony dependent modulation of rat deep cerebellar nuclear activity.

Authors:  Tianyu Tang; Timothy A Blenkinsop; Eric J Lang
Journal:  Elife       Date:  2019-01-09       Impact factor: 8.140

4.  Modular output circuits of the fastigial nucleus for diverse motor and nonmotor functions of the cerebellar vermis.

Authors:  Hirofumi Fujita; Takashi Kodama; Sascha du Lac
Journal:  Elife       Date:  2020-07-08       Impact factor: 8.140

5.  Cerebellum involvement in cortical sensorimotor circuits for the control of voluntary movements.

Authors:  Rémi D Proville; Maria Spolidoro; Nicolas Guyon; Guillaume P Dugué; Fekrije Selimi; Philippe Isope; Daniela Popa; Clément Léna
Journal:  Nat Neurosci       Date:  2014-07-27       Impact factor: 24.884

6.  Cerebellar zonal patterning relies on Purkinje cell neurotransmission.

Authors:  Joshua J White; Marife Arancillo; Trace L Stay; Nicholas A George-Jones; Sabrina L Levy; Detlef H Heck; Roy V Sillitoe
Journal:  J Neurosci       Date:  2014-06-11       Impact factor: 6.167

7.  Neuronal Regulation of Fast Synaptotagmin Isoforms Controls the Relative Contributions of Synchronous and Asynchronous Release.

Authors:  Josef Turecek; Wade G Regehr
Journal:  Neuron       Date:  2019-02-04       Impact factor: 17.173

8.  Local changes in the excitability of the cerebellar cortex produce spatially restricted changes in complex spike synchrony.

Authors:  Sarah P Marshall; Eric J Lang
Journal:  J Neurosci       Date:  2009-11-11       Impact factor: 6.167

9.  Reliable coding emerges from coactivation of climbing fibers in microbands of cerebellar Purkinje neurons.

Authors:  Ilker Ozden; Megan R Sullivan; H Megan Lee; Samuel S-H Wang
Journal:  J Neurosci       Date:  2009-08-26       Impact factor: 6.167

10.  Patterned neuroprotection in the Inpp4a(wbl) mutant mouse cerebellum correlates with the expression of Eaat4.

Authors:  Andrew J Sachs; Samuel A David; Neena B Haider; Arne M Nystuen
Journal:  PLoS One       Date:  2009-12-14       Impact factor: 3.240

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