Literature DB >> 15503131

Quantitative analysis of granule cell axons and climbing fiber afferents in the turtle cerebellar cortex.

D L Tolbert1, B Conoyer, M Ariel.   

Abstract

The turtle cerebellar cortex is a single flat sheet of gray matter that greatly facilitates quantitative analysis of biotylinated dextran amine labeled granule cell and olivocerebellar axons and Nissl-stained granule and Purkinje neurons. On average, ascending granule cell axons are relatively thicker than their parallel fiber branches (mean +/- SD: 0.84 +/- 0.17 vs 0.64 +/- 0.12 microm, respectively). Numerous en passant swellings, the site of presynaptic contact, were present on both ascending and parallel fiber granule cell axons. The swellings on ascending axons (1.82 +/- 0.34 microm, n = 52) were slightly larger than on parallel fibers (1.43 +/- 0.24 microm, n = 430). In addition, per unit length (100 microm) there were more swellings on ascending axons (11.2 +/- 4.2) than on parallel fibers (9.7 +/- 4.2). Each parallel fiber branch from an ascending axon is approximately 1.5 mm long. Olivocerebellar climbing fiber axons followed the highly tortuous dendrites of Purkinje cells in the inner most 15-20% of the molecular layer. Climbing fibers displayed relatively fewer en passant swellings. The spatial perimeter of climbing fiber arbors (area) increased 72% from anteriorly (1797 microm2) to posteriorly (3090 microm2) and 104% from medially (1690 microm2) to laterally (3450 microm2). Differences in the size and spacing of en passant swellings on granule cell axons suggest that ascending axons may have a functionally more significant impact on the excitability of a limited number of radially overlying Purkinje cells than the single contacts by parallel fiber with multiple orthogonally aligned Purkinje cell dendrites. The spatially restricted distribution of climbing fibers to the inner most molecular layer, the paucity of en passant swellings, and different terminal arbor areas are enigmatic. Nevertheless, these finding provide important anatomical information for future optical imaging and electrophysiological experiments.

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Year:  2004        PMID: 15503131      PMCID: PMC2244589          DOI: 10.1007/s00429-004-0423-0

Source DB:  PubMed          Journal:  Anat Embryol (Berl)        ISSN: 0340-2061


  32 in total

1.  Ascending granule cell axon: an important component of cerebellar cortical circuitry.

Authors:  G Gundappa-Sulur; E De Schutter; J M Bower
Journal:  J Comp Neurol       Date:  1999-06-14       Impact factor: 3.215

2.  Morphological observations on the cerebellar cortex.

Authors:  V BRAITENBERG; R P ATWOOD
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Authors:  D L Tolbert; J M Alisky; B R Clark
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4.  Patches of synchronized activity in the cerebellar cortex evoked by mossy-fiber stimulation: questioning the role of parallel fibers.

Authors:  D Cohen; Y Yarom
Journal:  Proc Natl Acad Sci U S A       Date:  1998-12-08       Impact factor: 11.205

5.  Quantitative analysis of cuneocerebellar projections in rats: differential topography in the anterior and posterior lobes.

Authors:  D L Tolbert; J C Gutting
Journal:  Neuroscience       Date:  1997-09       Impact factor: 3.590

6.  Morphology of parallel fibres in the cerebellar cortex of the rat: an experimental light and electron microscopic study with biocytin.

Authors:  C Pichitpornchai; J A Rawson; S Rees
Journal:  J Comp Neurol       Date:  1994-04-08       Impact factor: 3.215

Review 7.  Use of voltage-sensitive dyes and optical recordings in the central nervous system.

Authors:  T J Ebner; G Chen
Journal:  Prog Neurobiol       Date:  1995-08       Impact factor: 11.685

8.  Morphology of basal optic tract terminals in the turtle, Pseudemys scripta elegans.

Authors:  J Martin; N Kogo; M Ariel
Journal:  J Comp Neurol       Date:  1998-04-13       Impact factor: 3.215

9.  Quantitative analysis of converging spinal and cuneate mossy fibre afferent projections to the rat cerebellar anterior lobe.

Authors:  J M Alisky; D L Tolbert
Journal:  Neuroscience       Date:  1997-09       Impact factor: 3.590

10.  Morphology of single olivocerebellar axons labeled with biotinylated dextran amine in the rat.

Authors:  I Sugihara; H Wu; Y Shinoda
Journal:  J Comp Neurol       Date:  1999-11-15       Impact factor: 3.215

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  7 in total

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Journal:  J Neurophysiol       Date:  2010-12-22       Impact factor: 2.714

2.  Topography and response timing of intact cerebellum stained with absorbance voltage-sensitive dye.

Authors:  Michael E Brown; Michael Ariel
Journal:  J Neurophysiol       Date:  2008-11-12       Impact factor: 2.714

3.  Origin and timing of voltage-sensitive dye signals within layers of the turtle cerebellar cortex.

Authors:  Michael Ariel; Michael E Brown
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4.  Diffusion of flexible random-coil dextran polymers measured in anisotropic brain extracellular space by integrative optical imaging.

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5.  Model-founded explorations of the roles of molecular layer inhibition in regulating purkinje cell responses in cerebellar cortex: more trouble for the beam hypothesis.

Authors:  James M Bower
Journal:  Front Cell Neurosci       Date:  2010-08-27       Impact factor: 5.505

6.  Topography of Purkinje cells and other calbindin-immunoreactive cells within adult and hatchling turtle cerebellum.

Authors:  Michael Ariel; Kyle C Ward; Daniel L Tolbert
Journal:  Cerebellum       Date:  2009-06-23       Impact factor: 3.847

7.  Solenoidal Micromagnetic Stimulation Enables Activation of Axons With Specific Orientation.

Authors:  Laleh Golestanirad; John T Gale; Nauman F Manzoor; Hyun-Joo Park; Lyall Glait; Frederick Haer; James A Kaltenbach; Giorgio Bonmassar
Journal:  Front Physiol       Date:  2018-07-27       Impact factor: 4.566

  7 in total

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