Literature DB >> 9034878

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

S A Gilmore1, T J Sims.   

Abstract

This review summarises some of the major findings derived from studies using the model of a glia-depleted environment developed and characterised in this laboratory. Glial depletion is achieved by exposure of the immature rodent spinal cord to x-radiation which markedly reduces both astrocyte and oligodendrocyte populations and severely impairs myelination. This glia-depleted, hypomyelinated state presents a unique opportunity to examine aspects of spinal cord maturation in the absence of a normal glial population. An associated sequela within 2-3 wk following irradiation is the appearance of Schwann cells in the dorsal portion of the spinal cord. Characteristics of these intraspinal Schwann cells, their patterns of myelination or ensheathment, and their interrelations with the few remaining central glia have been examined. A later sequela is the development of Schwann cells in the ventral aspect of the spinal cord where they occur predominantly in the grey matter. Characteristics of these ventrally situated intraspinal Schwann cells are compared with those of Schwann cells located dorsally. Recently, injury responses have been defined in the glia-depleted spinal cord subsequent to the lesioning of dorsal spinal nerve roots. In otherwise normal animals, dorsal nerve root injury induces an astrocytic reaction within the spinal segments with which the root(s) is/are associated. Lesioning of the 4th lumbar dorsal root on the right side in irradiated or nonirradiated animals results in markedly different glial responses with little astrocytic scarring in the irradiated animals. Tracing studies reveal that these lesioned dorsal root axons regrow rather robustly into the spinal cord in irradiated but not in nonirradiated animals. To examine role(s) of glial cells in preventing this axonal regrowth, glial cells are now being added back to this glia-depleted environment through transplantation of cultured glia into the irradiated area. Transplanted astrocytes establish barrier-like arrangements within the irradiated cords and prevent axonal regrowth into the cord. Studies using other types of glial cultures (oligodendrocyte or mixed) are ongoing.

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Mesh:

Year:  1997        PMID: 9034878      PMCID: PMC1467580          DOI: 10.1046/j.1469-7580.1997.19010005.x

Source DB:  PubMed          Journal:  J Anat        ISSN: 0021-8782            Impact factor:   2.610


  41 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.  Ultrastructural and light-microscopic studies of the nodal region in large myelinated fibres of the adult feline spinal cord white matter.

Authors:  C Hildebrand
Journal:  Acta Physiol Scand Suppl       Date:  1971

3.  A light microscopic study of the effects of X-irradiation on the spinal cord of neonatal rats.

Authors:  J A Beal; J L Hall
Journal:  J Neuropathol Exp Neurol       Date:  1974-01       Impact factor: 3.685

4.  Degeneration of dorsal roots in the adult rat spinal cord.

Authors:  E J Nathaniel; D R Nathaniel
Journal:  Exp Neurol       Date:  1973-08       Impact factor: 5.330

5.  Autoradiographic studies of intramedullary Schwann cells in irradiated spinal cords of immature rats.

Authors:  S A Gilmore
Journal:  Anat Rec       Date:  1971-12

6.  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

7.  Remyelination of CNS axons by Schwann cells transplanted from the sciatic nerve.

Authors:  W F Blakemore
Journal:  Nature       Date:  1977-03-03       Impact factor: 49.962

8.  Astroglial response to degeneration of dorsal root fibers in adult rat spinal cord.

Authors:  E J Nathaniel; D R Nathaniel
Journal:  Exp Neurol       Date:  1977-01       Impact factor: 5.330

9.  Glial bridges and Schwann cell migration during chronic demyelination in the C.N.S.

Authors:  C S Raine; U Traugott; S H Stone
Journal:  J Neurocytol       Date:  1978-10

10.  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
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  3 in total

Review 1.  The transitional zone and CNS regeneration.

Authors:  J P Fraher
Journal:  J Anat       Date:  1999-02       Impact factor: 2.610

2.  The repair function of the multifunctional DNA repair/redox protein APE1 is neuroprotective after ionizing radiation.

Authors:  Michael R Vasko; Chunlu Guo; Eric L Thompson; Mark R Kelley
Journal:  DNA Repair (Amst)       Date:  2011-07-08

3.  A selective glial barrier at motor axon exit points prevents oligodendrocyte migration from the spinal cord.

Authors:  Sarah Kucenas; Wen-Der Wang; Ela W Knapik; Bruce Appel
Journal:  J Neurosci       Date:  2009-12-02       Impact factor: 6.167

  3 in total

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