Literature DB >> 8382572

Cytoskeletal changes and ubiquitin expression in dystrophic axons of Seitelberger's disease.

G Moretto1, M Sparaco, S Monaco, B Bonetti, N Rizzuto.   

Abstract

Central nervous system specimens of 4 cases of Infantile Neuroaxonal Dystrophy (Seitelberger's disease) were processed for Bodian's silver stain and for immunostaining with antibodies against neurofilaments (NF), tubulin and ubiquitin (UBQ). Reactivity to NF and UBQ was restricted to spheroids of small size; swellings larger than 30 mu were negative, in spite of their positivity to Bodian's silver stain. Reactivity to tubulin was evident only in normal fibers, whereas no positive material was observed in dystrophic axons. These findings suggest that loss of microtubules (MT) and denaturation of NF might play a crucial role in the mechanisms responsible for the formation of axonal spheroids; in addition the focal activation of the UBQ system suggests an attempt of the neuron to remove abnormal material even at sites remote from the perikaryon.

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Year:  1993        PMID: 8382572

Source DB:  PubMed          Journal:  Clin Neuropathol        ISSN: 0722-5091            Impact factor:   1.368


  4 in total

1.  Amyloid beta precursor protein and ubiquitin epitopes in human and experimental dystrophic axons. Ultrastructural localization.

Authors:  B Bacci; E Cochran; M G Nunzi; E Izeki; T Mizutani; A Patton; S Hite; L M Sayre; L Autilio-Gambetti; P Gambetti
Journal:  Am J Pathol       Date:  1994-04       Impact factor: 4.307

2.  Expression of ubiquitin-like immunoreactivity in axons after compression trauma to rat spinal cord.

Authors:  G L Li; M Farooque
Journal:  Acta Neuropathol       Date:  1996       Impact factor: 17.088

3.  Spontaneous murine neuroaxonal dystrophy: a model of infantile neuroaxonal dystrophy.

Authors:  D M Bouley; J J McIntire; B T Harris; R J Tolwani; G M Otto; R H DeKruyff; S J Hayflick
Journal:  J Comp Pathol       Date:  2006-03-20       Impact factor: 1.311

4.  Ultrastructure and immunoreactivity of dystrophic axons indicate a different pathogenesis of Hallervorden-Spatz disease and infantile neuroaxonal dystrophy.

Authors:  A Malandrini; T Cavallaro; G M Fabrizi; G Berti; R Salvestroni; C Salvadori; G C Guazzi
Journal:  Virchows Arch       Date:  1995       Impact factor: 4.064

  4 in total

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