Literature DB >> 16041715

Developmental modifications of olivocerebellar topography: the granuloprival cerebellum reveals multiple routes from the inferior olive.

Betty Fournier1, Ann M Lohof, Adrian J Bower, Jean Mariani, Rachel M Sherrard.   

Abstract

Correct function of neural circuits depends on highly organized neuronal connections, refined from less precise projections through synaptic elimination, collateral regression, or neuronal death. We examined regressive phenomena that define olivocerebellar topography during maturation from Purkinje cell polyinnervation to monoinnervation. We used bilateral retrograde tracing to determine the source of olivocerebellar afferents to posterior vermis lobules VII-VIII in a model of retained immature Purkinje cell polyinnervation, the granuloprival cerebellum. In controls, labelled neurons were found only in the contralateral inferior olive (ION) clustered in a small ventromedial locus that is congruent with known olivocerebellar topography. In granuloprival animals, olivary labelling appeared more dispersed and was present in homologous ipsilateral regions. Double-labelled neurons were never seen. Retrograde tracing following unilateral olivocerebellar transection in adult granuloprival rats revealed: 1) the origin of the normal (remaining) path projecting through the contralateral inferior peduncle was more localized than in irradiated nonpedunculotomized rats, 2) a small double-crossed path, and 3) a projection that ascends the peduncle ipsilateral to the ION of origin, part of which crosses the midline within the cerebellum. Electrophysiological and immunohistochemical assessment in the neonatal cerebellum revealed that transcommissural paths are not present during development but sprout within the irradiated cerebellum. Therefore, the olivocerebellar projection in the granuloprival rat, as a model of the immature path, shows parasagittal organization similar to that of controls in its normally crossed path but possesses additional abnormal projections. Thus, maturation of olivocerebellar topography involves removal of whole developmental paths to define laterality plus synapse elimination within largely predefined parasagittal zones. Copyright (c) 2005 Wiley-Liss, Inc.

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Year:  2005        PMID: 16041715     DOI: 10.1002/cne.20648

Source DB:  PubMed          Journal:  J Comp Neurol        ISSN: 0021-9967            Impact factor:   3.215


  5 in total

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Authors:  Mathieu Letellier; Yannick Bailly; Valérie Demais; Rachel M Sherrard; Jean Mariani; Ann M Lohof
Journal:  J Neurosci       Date:  2007-05-16       Impact factor: 6.167

2.  Formation and reformation of climbing fibre synapses in the cerebellum: a similar story?

Authors:  Rachel M Sherrard; Mathieu Letellier; Ann M Lohof; Jean Mariani
Journal:  Cerebellum       Date:  2013-06       Impact factor: 3.847

Review 3.  What does low-intensity rTMS do to the cerebellum?

Authors:  N Morellini; S Grehl; A Tang; J Rodger; J Mariani; A M Lohof; R M Sherrard
Journal:  Cerebellum       Date:  2015-02       Impact factor: 3.847

4.  The Roles of the Olivocerebellar Pathway in Motor Learning and Motor Control. A Consensus Paper.

Authors:  Eric J Lang; Richard Apps; Fredrik Bengtsson; Nadia L Cerminara; Chris I De Zeeuw; Timothy J Ebner; Detlef H Heck; Dieter Jaeger; Henrik Jörntell; Mitsuo Kawato; Thomas S Otis; Ozgecan Ozyildirim; Laurentiu S Popa; Alexander M B Reeves; Nicolas Schweighofer; Izumi Sugihara; Jianqiang Xiao
Journal:  Cerebellum       Date:  2017-02       Impact factor: 3.847

5.  Cerebellar Nuclei Neurons Show Only Small Excitatory Responses to Optogenetic Olivary Stimulation in Transgenic Mice: In Vivo and In Vitro Studies.

Authors:  Huo Lu; Bo Yang; Dieter Jaeger
Journal:  Front Neural Circuits       Date:  2016-03-24       Impact factor: 3.492

  5 in total

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