Literature DB >> 6321565

Postnatal development of the inferior olivary complex in the rat. II. Topographic organization of the immature olivocerebellar projection.

C Sotelo, F Bourrat, A Triller.   

Abstract

The state of organization of the olivocerebellar projection in newborn and 5-day-old rats has been analyzed by autoradiography of anterogradely transported 3H-leucine, as well as by retrograde transport of horseradish peroxidase. The efferent axons of the inferior olivary neurons are already present and already highly organized in the cerebellum of newborn rats. Most of the autoradiographic labelling subsequent to the injection of 3H-leucine into the inferior olive is seen in the subcortical medullary zone. Labelled axons only partially invade the gray matter, where they reach the zone occupied by randomly distributed Purkinje cells. At this immature stage, olivocerebellar projections are already entirely crossed and distributed according to a pattern which is similar to the adult. At the fifth postnatal day olivocerebellar projections have moved from the medullary zone toward the interface between the molecular and the granular layers where Purkinje cells have arranged in a monolayer. Evidence for translocation of climbing fibers from their perisomatic to their peridendritic position is already distinct in these young cerebella. Combination of anterograde and retrograde fiber system tracing experiments discloses the following crossed topography of olivocerebellar projections: The caudal half of the medial accessory olive projects mainly to the vermis of the posterior lobe, whereas its rostral half projects to the flocculus, paraflocculus, and the intermediate cortex. The principal olive, ventral and dorsal lamellae, supplies climbing fiber inputs to the hemispheric cortex. The caudal half of the dorsal accessory olive projects to the lateral portion of the vermis of the anterior lobe, whereas neurons in its rostral half send their axons toward the intermediate cortex. This topographic arrangement is, therefore, similar to that reported for adult mammals. The present results, alone or when compared with those obtained during other studies on the synaptogenesis between climbing fibers and Purkinje cells, allow the following conclusions: The climbing fibers enter the cerebellar cortex before Purkinje cells have reached the developmental phase compatible with synaptogenesis. They wait in the medullary white matter until appropriate maturation of their cellular targets. Olivocerebellar topography is roughly similar in newborn, 5-day -old, and adult rats. Synaptogenesis between climbing fibers and Purkinje cells, which is known not to start before the second postnatal day, is not necessary for the establishment of the topographic organization of the olivocerebellar projection.

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Year:  1984        PMID: 6321565     DOI: 10.1002/cne.902220204

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


  22 in total

1.  Spatiotemporal expression patterns of metalloproteinases and their inhibitors in the postnatal developing rat cerebellum.

Authors:  C Vaillant; M Didier-Bazès; A Hutter; M F Belin; N Thomasset
Journal:  J Neurosci       Date:  1999-06-15       Impact factor: 6.167

Review 2.  Mechanisms of glial-guided neuronal migration in vitro and in vivo.

Authors:  M E Hatten; C A Mason
Journal:  Experientia       Date:  1990-09-15

3.  Compartmentation in mammalian cerebellum: Zebrin II and P-path antibodies define three classes of sagittally organized bands of Purkinje cells.

Authors:  N Leclerc; G A Schwarting; K Herrup; R Hawkes; M Yamamoto
Journal:  Proc Natl Acad Sci U S A       Date:  1992-06-01       Impact factor: 11.205

4.  Grafts of dissociated cerebellar cells containing Purkinje cell precursors organize into zebrin I defined compartments.

Authors:  R V Rouse; C Sotelo
Journal:  Exp Brain Res       Date:  1990       Impact factor: 1.972

5.  Transient synaptic redundancy in the developing cerebellum and isostatic random stacking of hard spheres.

Authors:  F Eddi; J Mariani; G Waysand
Journal:  Biol Cybern       Date:  1996-02       Impact factor: 2.086

6.  Development and migration of Purkinje cells in the mouse cerebellar primordium.

Authors:  S Yuasa; K Kawamura; K Ono; T Yamakuni; Y Takahashi
Journal:  Anat Embryol (Berl)       Date:  1991

Review 7.  Aldolase C/zebrin II and the regionalization of the cerebellum.

Authors:  R Hawkes; K Herrup
Journal:  J Mol Neurosci       Date:  1995       Impact factor: 3.444

8.  Olivocerebellar climbing fibers in the granuloprival cerebellum: morphological study of individual axonal projections in the X-irradiated rat.

Authors:  I Sugihara; Y Bailly; J Mariani
Journal:  J Neurosci       Date:  2000-05-15       Impact factor: 6.167

9.  An immunohistochemical study of serotonin development in the opossum cerebellum.

Authors:  G A Bishop; R H Ho; J S King
Journal:  Anat Embryol (Berl)       Date:  1985

10.  The olivocerebellar projection in normal (+/+), heterozygous weaver (wv/+), and homozygous weaver (wv/wv) mutant mice: comparison of terminal pattern and topographic organization.

Authors:  G J Blatt; L M Eisenman
Journal:  Exp Brain Res       Date:  1993       Impact factor: 1.972

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