Literature DB >> 4075120

Dependence of axolemmal differentiation on contact with glial cells in chronically demyelinated lesions of cat spinal cord.

J Rosenbluth, J H Tao-Cheng, W F Blakemore.   

Abstract

Chronically demyelinated lesions of cat dorsal columns were created by focal injection of the glial toxin ethidium bromide. Freeze-fracture studies show that the center of the lesion, which is devoid of glial cells and processes, contains axons having neither node-like nor paranodal-type membrane specializations. Near the margin of the lesion, however, where axons are in contact with glial cells, the axolemma sometimes displays focal accumulations of E- and P-face particles resembling those at nodes of Ranvier. In cases where the adjacent cell could be identified, it had the characteristics of an astrocyte. Linear indentations of the axolemma displaying a paracrystalline pattern like that of the paranodal axolemma also occur in the marginal region. Here, the adjacent cell had the characteristics of an oligodendrocyte. These specializations may be closely associated with each other or spatially separate. Normal nodal and paranodal specializations were absent throughout the lesion at all time periods examined. These findings support the view that both the formation and the maintenance of nodal and paranodal axon membrane specializations require contact with glial cells.

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Year:  1985        PMID: 4075120     DOI: 10.1016/0006-8993(85)90973-4

Source DB:  PubMed          Journal:  Brain Res        ISSN: 0006-8993            Impact factor:   3.252


  5 in total

1.  Early events in node of Ranvier formation during myelination and remyelination in the PNS.

Authors:  Dorothy P Schafer; Andrew W Custer; Peter Shrager; Matthew N Rasband
Journal:  Neuron Glia Biol       Date:  2006-05

2.  Conduction in segmentally demyelinated mammalian central axons.

Authors:  P A Felts; T A Baker; K J Smith
Journal:  J Neurosci       Date:  1997-10-01       Impact factor: 6.167

3.  The interaction of Schwann cells with CNS axons in regions containing normal astrocytes.

Authors:  W F Blakemore; A J Crang; R Curtis
Journal:  Acta Neuropathol       Date:  1986       Impact factor: 17.088

Review 4.  The pathophysiology of multiple sclerosis: the mechanisms underlying the production of symptoms and the natural history of the disease.

Authors:  K J Smith; W I McDonald
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  1999-10-29       Impact factor: 6.237

Review 5.  Sodium channels and multiple sclerosis: roles in symptom production, damage and therapy.

Authors:  Kenneth J Smith
Journal:  Brain Pathol       Date:  2007-04       Impact factor: 6.508

  5 in total

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