Literature DB >> 8821440

Sprouting of crossed entorhinodentate fibers after a unilateral entorhinal lesion: anterograde tracing of fiber reorganization with Phaseolus vulgaris-leucoagglutinin (PHAL).

T Deller1, M Frotscher, R Nitsch.   

Abstract

Fibers from the contralateral entorhinal cortex (EC) to the dentate gyrus partially replace the input lost after an ipsilateral EC lesion. To study the morphology and course of single sprouted crossed entorhinodentate fibers, the anterograde tracer Phaseolus vulgaris-leucoagglutinin (PHAL) was used. Rats that survived for 4 to 8 weeks after a unilateral entorhinal lesion received PHAL deposits into the entorhinal cortex contralateral to the lesion. Control animals received a similar PHAL deposit. Single PHAL-labeled fibers in the molecular layer of the contralateral (EC lesion) fascia dentata were drawn with a camera lucida, and an axon-branching index (branch points/100 microns axon length) was calculated for these crossed entorhinodentate fibers in controls and operated animals. In animals with EC lesions, the density of PHAL-labeled crossed entorhinodentate fibers had increased remarkably. Single crossed entorhinodentate axons showed significantly more axon branch points in experimental than in control animals. In addition, some axon segments displayed high densities of small axonal extensions. Frequently, tanglelike structures were observed in the denervated outer molecular layer. These tangles consisted of one or more PHAL-labeled axons that intertwined and formed an axon tangle filled completely with branches, extensions, and boutons. Our data indicate that crossed EC fibers sprout by forming additional collaterals, axonal extensions, and tangles. Abnormal neurite formations are a characteristic feature of plaques in Alzheimer's disease. Future studies must be done to show whether or not there is a close relationship between axonal tangles and plaques in Alzheimer's disease, which, like the present lesion paradigm, severely affects entorhinal projection neurons.

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Year:  1996        PMID: 8821440     DOI: 10.1002/(SICI)1096-9861(19960129)365:1<42::AID-CNE4>3.0.CO;2-J

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


  6 in total

1.  Organization of identified fiber tracts in the rat fimbria-fornix: an anterograde tracing and electron microscopic study.

Authors:  G Adelmann; T Deller; M Frotscher
Journal:  Anat Embryol (Berl)       Date:  1996-05

2.  A novel entorhinal projection to the rat dentate gyrus: direct innervation of proximal dendrites and cell bodies of granule cells and GABAergic neurons.

Authors:  T Deller; A Martinez; R Nitsch; M Frotscher
Journal:  J Neurosci       Date:  1996-05-15       Impact factor: 6.167

3.  Endogenous FGF-2 is important for cholinergic sprouting in the denervated hippocampus.

Authors:  A M Fagan; S T Suhr; C A Lucidi-Phillipi; D A Peterson; D M Holtzman; F H Gage
Journal:  J Neurosci       Date:  1997-04-01       Impact factor: 6.167

4.  Differential regulation of ciliary neurotrophic factor (CNTF) and CNTF receptor alpha expression in astrocytes and neurons of the fascia dentata after entorhinal cortex lesion.

Authors:  M Y Lee; T Deller; M Kirsch; M Frotscher; H D Hofmann
Journal:  J Neurosci       Date:  1997-02-01       Impact factor: 6.167

5.  Crossed Entorhino-Dentate Projections Form and Terminate With Correct Layer-Specificity in Organotypic Slice Cultures of the Mouse Hippocampus.

Authors:  Lars Hildebrandt-Einfeldt; Kenrick Yap; Mandy H Paul; Carolin Stoffer; Nadine Zahn; Alexander Drakew; Maximilian Lenz; Andreas Vlachos; Thomas Deller
Journal:  Front Neuroanat       Date:  2021-02-11       Impact factor: 3.856

Review 6.  Structural plasticity in the dentate gyrus- revisiting a classic injury model.

Authors:  Julia V Perederiy; Gary L Westbrook
Journal:  Front Neural Circuits       Date:  2013-02-18       Impact factor: 3.492

  6 in total

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