Literature DB >> 1865015

Reinnervation of cerebellar Purkinje cells by climbing fibres surviving a subtotal lesion of the inferior olive in the adult rat. I. Development of new collateral branches and terminal plexuses.

F Rossi1, L Wiklund, J J van der Want, P Strata.   

Abstract

Cerebellar climbing fibres react by collateral sprouting after subtotal lesions of the inferior olive, and the newly formed branches are able to reinnervate neighbouring denervated Purkinje cells. In the present paper, we used the Phaseolus vulgaris leucoagglutinin (PHA-L) tracing technique to label the climbing fibres and study their plasticity in detail at the light microscopical level. The specific objectives were to study the time course and morphological aspects of their sprouting, to estimate their extent of growth, and to compare the newly formed terminal plexuses with normal climbing fibres. Intraperitoneal injection of 3-acetylpyridine induced degeneration of the majority of the olivary neurones, which terminate as climbing fibres in the cerebellar cortex. Regularly, small numbers of neurones survived in the inferior olive. In the cerebellar cortex scattered surviving climbing fibres were found, which were devoid of any sign of injury. Already 3 days after the lesion, surviving climbing fibres had emitted collateral branches, which elongated for some distance through the molecular layer and ended with a number of varicosities and very fine branchlets. By 7 days, it was possible to recognize new developing arbours which grew in the molecular layer with the same orientation as normal climbing fibres. At longer survival times, extensive terminal arbours had developed and double labelling experiments confirmed that they terminated around the proximal dendrites of Purkinje cells. The newly formed terminal plexuses resembled, in all essential aspects, normal climbing fibres. In addition, from 1 month onward, it was evident that every surviving climbing fibre was able to form several new terminal plexuses reinnervating a number of neighbouring Purkinje cells. The result of this process was the formation of large clusters of newly formed plexuses around the parental arborization. Quantitative estimates indicated that the domain of innervation of single surviving climbing fibres could be increased by more than six times. It is concluded that climbing fibres surviving a subtotal olivary lesion are capable of extensive sprouting, axonal growth, and formation of new terminal plexuses, which resemble normal climbing fibres. Previous electrophysiological evidence indicates that this reinnervation is functional. The high specificity with which sprouting olivary axons reinnervate the proximal Purkinje cell dendrites suggests the existence of precise interactions between the growing fibres and their target. This example of "homotypic" collateral sprouting and reinnervation may thus provide a useful model for the study of nerve-target interactions.

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Year:  1991        PMID: 1865015     DOI: 10.1002/cne.903080403

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


  23 in total

1.  Compensatory restorative processes and operant reflexes in rats after neurotoxin lesioning of the inferior olive.

Authors:  V V Fanardzhyan; E A Oganesyan; A B Melik-Musyan; E V Papoyan; O V Govorkyan
Journal:  Neurosci Behav Physiol       Date:  1999 Nov-Dec

2.  The olivocerebellar projection mediates ibogaine-induced degeneration of Purkinje cells: a model of indirect, trans-synaptic excitotoxicity.

Authors:  E O'Hearn; M E Molliver
Journal:  J Neurosci       Date:  1997-11-15       Impact factor: 6.167

3.  Axonal motility and its modulation by activity are branch-type specific in the intact adult cerebellum.

Authors:  Hiroshi Nishiyama; Masahiro Fukaya; Masahiko Watanabe; David J Linden
Journal:  Neuron       Date:  2007-11-08       Impact factor: 17.173

4.  Reinnervation of late postnatal Purkinje cells by climbing fibers: neosynaptogenesis without transient multi-innervation.

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

5.  Long-term in vivo time-lapse imaging of synapse development and plasticity in the cerebellum.

Authors:  Naoko Nishiyama; Jeremy Colonna; Elise Shen; Jennifer Carrillo; Hiroshi Nishiyama
Journal:  J Neurophysiol       Date:  2013-10-16       Impact factor: 2.714

6.  Control of spine formation by electrical activity in the adult rat cerebellum.

Authors:  M Bravin; L Morando; A Vercelli; F Rossi; P Strata
Journal:  Proc Natl Acad Sci U S A       Date:  1999-02-16       Impact factor: 11.205

7.  Symposium in honor of Ferdinando Rossi: a passionate journey through the cerebellar mysteries.

Authors:  K Leto; D Carulli; A Buffo
Journal:  Cerebellum       Date:  2014-12       Impact factor: 3.847

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.  GluRdelta2 expression in the mature cerebellum of hotfoot mice promotes parallel fiber synaptogenesis and axonal competition.

Authors:  Georgia Mandolesi; Eleonora Autuori; Roberta Cesa; Federica Premoselli; Paolo Cesare; Piergiorgio Strata
Journal:  PLoS One       Date:  2009-04-16       Impact factor: 3.240

10.  Neuronal nicotinic receptor agonists improve gait and balance in olivocerebellar ataxia.

Authors:  L Wecker; M E Engberg; R M Philpot; C S Lambert; C W Kang; J C Antilla; P C Bickford; C E Hudson; T A Zesiewicz; Peter P Rowell
Journal:  Neuropharmacology       Date:  2013-05-24       Impact factor: 5.250

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