Literature DB >> 15102908

Differential maturation of climbing fiber innervation in cerebellar vermis.

Hiroshi Nishiyama1, David J Linden.   

Abstract

Folding of the brain surface is a general morphological adaptation to maximize surface area in a limited cranial volume. Surface folding is present not only in the neocortex but also in the cerebellar cortex. This folding creates subdivisions of the cortical surface: the sulci, the gyri, and the straight bank region, which is interposed. Is cortical folding only the solution to a surface-volume problem or does it also confer functional differences on the subdivisions that are created by this geometry? Here we have used the innervation of Purkinje cells by climbing fibers as a model system to explore potential functional differences. Purkinje cells are innervated by multiple climbing fibers at birth but undergo an activity-dependent refinement, such that by postnatal day (P) 21, most are contacted by a single climbing fiber. Using whole-cell recording from slices of cerebellar vermis derived from juvenile (P18-25) or adult (P60-83) mice, we found that significantly more Purkinje cells in the sulcus were innervated by multiple climbing fibers than in the gyrus or bank subdivisions; however, the basic properties of climbing fiber-Purkinje cell EPSCs such as kinetics, amplitude, and paired-pulse ratio were similar across cortical subdivisions. To search for a morphological correlate of differential multiple climbing fiber innervation, we labeled climbing fibers and performed reconstructions of immunofluorescent images. These revealed that, unlike the bank-gyrus subdivisions, most of the climbing fibers in the sulcus do not innervate the superficial molecular layer. These findings suggest that the subdivisions of the cerebellar cortex produced by folding may create functionally distinct entities.

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Year:  2004        PMID: 15102908      PMCID: PMC6729416          DOI: 10.1523/JNEUROSCI.5610-03.2004

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


  18 in total

1.  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

2.  Impaired motor learning in the vestibulo-ocular reflex in mice with multiple climbing fiber input to cerebellar Purkinje cells.

Authors:  Rhea R Kimpo; Jennifer L Raymond
Journal:  J Neurosci       Date:  2007-05-23       Impact factor: 6.167

3.  Neuron density and serotonin receptor binding in prefrontal cortex in suicide.

Authors:  Mark D Underwood; Suham A Kassir; Mihran J Bakalian; Hanga Galfalvy; J John Mann; Victoria Arango
Journal:  Int J Neuropsychopharmacol       Date:  2011-05-09       Impact factor: 5.176

4.  Neuronal Nogo-A negatively regulates dendritic morphology and synaptic transmission in the cerebellum.

Authors:  Marija M Petrinovic; Raphael Hourez; Elisabeth M Aloy; Gregoire Dewarrat; David Gall; Oliver Weinmann; Julien Gaudias; Lukas C Bachmann; Serge N Schiffmann; Kaspar E Vogt; Martin E Schwab
Journal:  Proc Natl Acad Sci U S A       Date:  2012-12-31       Impact factor: 11.205

5.  Spontaneous cluster activity in the inferior olivary nucleus in brainstem slices from postnatal mice.

Authors:  Jens C Rekling; Kristian H R Jensen; Henrik Jahnsen
Journal:  J Physiol       Date:  2012-01-16       Impact factor: 5.182

6.  Digital morphometry of rat cerebellar climbing fibers reveals distinct branch and bouton types.

Authors:  Kerry M Brown; Izumi Sugihara; Yoshikazu Shinoda; Giorgio A Ascoli
Journal:  J Neurosci       Date:  2012-10-17       Impact factor: 6.167

7.  Cytoplasmic polyadenylation element binding protein 1-mediated mRNA translation in Purkinje neurons is required for cerebellar long-term depression and motor coordination.

Authors:  Michael McEvoy; Guan Cao; Paula Montero Llopis; Mitchell Kundel; Kendrick Jones; Catherine Hofler; Chan Shin; David G Wells
Journal:  J Neurosci       Date:  2007-06-13       Impact factor: 6.167

8.  TrkB is necessary for pruning at the climbing fibre-Purkinje cell synapse in the developing murine cerebellum.

Authors:  Erin M Johnson; Ethan T Craig; Hermes H Yeh
Journal:  J Physiol       Date:  2007-04-26       Impact factor: 5.182

9.  H2-K(b) and H2-D(b) regulate cerebellar long-term depression and limit motor learning.

Authors:  Michael J McConnell; Yanhua H Huang; Akash Datwani; Carla J Shatz
Journal:  Proc Natl Acad Sci U S A       Date:  2009-04-03       Impact factor: 11.205

Review 10.  Interactions Between Purkinje Cells and Granule Cells Coordinate the Development of Functional Cerebellar Circuits.

Authors:  Meike E van der Heijden; Roy V Sillitoe
Journal:  Neuroscience       Date:  2020-06-14       Impact factor: 3.590

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