Literature DB >> 2744109

Interactions between Schwann cells and CNS axons following a delay in the normal formation of central myelin.

T J Sims1, S A Gilmore.   

Abstract

Irradiation of the rat spinal cord during the first postnatal week results in a profound reduction of oligodendrocyte myelin formation in the dorsal funiculi (DF). Despite this absence of myelin, however, axons in the irradiated region in the DF increase in diameter and approximate the size distribution seen in the control spinal cord. By 25 days of age Schwann cells are present in the irradiated DF where they undergo cell division and myelinate the axons. During the early stages of this myelin formation, these intraspinal Schwann cells exhibit a relationship to axons that is somewhat different from that seen in the normal developing peripheral nervous system (PNS). For example, within a given region, intraspinal Schwann cells myelinate axons of large diameter prior to ensheathing bundles of small diameter axons. Additionally, during myelination a Schwann cell will surround a single axon with multiple processes which appear to compete for contact with the axolemma. On axons of larger diameter, the elaboration of these processes is so excessive that it is often difficult to trace them back to the parent Schwann cell. Later, when a single process establishes several spirals about an axon, additional processes are no longer elaborated, and the "extra" processes disappear as myelin formation advances to the stage of compact lamellae. Thereafter, the myelin sheath continues to form in a normal manner. Excess processes have been observed during myelinogenesis in the normal developing PNS, but their frequency in that environment is much less than in the irradiated cord. These observations support the hypothesis that the signal(s) to initiate myelin formation are expressed on the axolemmal surface and are controlled by the neuron. In addition, these observations suggest that the delay in myelination results in an affinity or tropism between axons and Schwann cells which exceeds the level existing at the normal time of myelin formation.

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Year:  1989        PMID: 2744109     DOI: 10.1007/bf00249902

Source DB:  PubMed          Journal:  Exp Brain Res        ISSN: 0014-4819            Impact factor:   1.972


  25 in total

1.  The effects of x-irradiation on the spinal cords of neonatal rats. II. Histological observations.

Authors:  S A GILMORE
Journal:  J Neuropathol Exp Neurol       Date:  1963-04       Impact factor: 3.685

2.  Potential of Schwann cells from unmyelinated nerves to produce myelin: a quantitative ultrastructural and radiographic study.

Authors:  A J Aguayo; L Charron; G M Bray
Journal:  J Neurocytol       Date:  1976-10

3.  Schwann cell remyelination of CNS axons following injection of cultures of CNS cells into areas of persistent demyelination.

Authors:  W F Blakemore; A J Crang; R C Patterson
Journal:  Neurosci Lett       Date:  1987-06-01       Impact factor: 3.046

4.  The relationships between interphase Schwann cells and axons before myelination: a quantitative electron microscopic study.

Authors:  H D Webster; R Martin; M F O'Connell
Journal:  Dev Biol       Date:  1973-06       Impact factor: 3.582

5.  On the presence of peripheral-like nervous and connective tissue within irradiated spinal cord.

Authors:  S A Gilmore; D Duncan
Journal:  Anat Rec       Date:  1968-04

6.  Axolemma-enriched fractions isolated from PNS and CNS are mitogenic for cultured Schwann cells.

Authors:  G H DeVries; J L Salzer; R P Bunge
Journal:  Brain Res       Date:  1982-02       Impact factor: 3.252

7.  Intramedullary Schwann cell development following x-irradiation of mid-thoracic and lumbosacral spinal cord levels in immature rats.

Authors:  J K Heard; S A Gilmore
Journal:  Anat Rec       Date:  1980-05

8.  Inhibition of in vitro peripheral myelin formation by monoclonal anti-galactocerebroside.

Authors:  B Ranscht; P M Wood; R P Bunge
Journal:  J Neurosci       Date:  1987-09       Impact factor: 6.167

9.  Studies of Schwann cell proliferation. III. Evidence for the surface localization of the neurite mitogen.

Authors:  J L Salzer; R P Bunge; L Glaser
Journal:  J Cell Biol       Date:  1980-03       Impact factor: 10.539

10.  Myelin-specific proteins and glycolipids in rat Schwann cells and oligodendrocytes in culture.

Authors:  R Mirsky; J Winter; E R Abney; R M Pruss; J Gavrilovic; M C Raff
Journal:  J Cell Biol       Date:  1980-03       Impact factor: 10.539

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Review 2.  Glial-glial and glial-neuronal interfaces in radiation-induced, glia-depleted spinal cord.

Authors:  S A Gilmore; T J Sims
Journal:  J Anat       Date:  1997-01       Impact factor: 2.610

3.  Regeneration of dorsal root axons into experimentally altered glial environments in the rat spinal cord.

Authors:  T J Sims; S A Gilmore
Journal:  Exp Brain Res       Date:  1994       Impact factor: 1.972

4.  Possible synergistic effect of apoE and LRP1 genotypes on metabolic syndrome development in Serbian patients.

Authors:  N Vučinić; K Stankov; M Đan; I Barjaktarović; E Stokić; L J Strajnić; D Obreht; I Đan
Journal:  Mol Biol Rep       Date:  2019-09-20       Impact factor: 2.316

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