Literature DB >> 1133086

Abnormalities in Schwann cell sheaths in spinal nerve roots of dystrophic mice.

C A Stirling.   

Abstract

Dorsal and ventral spinal roots at cervical, thoracic, lumbar and sacral levels in dystrophic, dy/dy, mice of both 129/ReJ and C57Bl/6J phenotypes showed a complete lack of Schwann cell sheaths of any sort around the majority of their nerve fibres. This condition, termed amyelination, is more extensive (up to 1-5 cm in length) in the longer lumbar and sacral roots than in the shorter roots or in the proximal regions of the sciatic nerve which are also affected to some extent. Amyelination does not appear to be a consequence of myelin or Schwann cell degeneration, as debris is uncommon. Heterozygous carriers are not affected in any obvious way. Myelinated fibres, with Schwann cells of peripheral origin, occur immediately adjacent to the spinal cord in both dorsal and ventral roots, while in dorsal roots unmyelinated fibres also occur, as in normal animals. Amyelinated fibres begin to appear a few internodal lengths away from the cord and are present until near, or within, the dorsal root ganglion, where they become myelinated again. The portion of an axon which has no myelin begins at a normal appearing paranodal region (termed a half node of Ranvier) at the end of a myelin internode. Resumption of myelination likewise begins at a half node. A few myelinated axons may be seen in any given cross section of a root, but as a rule a given myelinated fibre does not remain myelinated throughout the whole length of the root. It is suggested that the nerve lesions develop where the nerves are lengthening rapidly as the animal grows and changes its shape. How these nerve changes release to those in muscle is conjectural.

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Year:  1975        PMID: 1133086      PMCID: PMC1231626     

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


  15 in total

1.  Survival of strain 129 dystrophic mice in parabiosis.

Authors:  R S POPE; E D MURPHY
Journal:  Am J Physiol       Date:  1960-12

2.  Evidence on inheritance of muscular dystrophy in an inbred strain of mice using ovarian transplantation.

Authors:  L C STEVENS; E S RUSSELL; J L SOUTHARD
Journal:  Proc Soc Exp Biol Med       Date:  1957-05

3.  Dystrophia Muscularis: A HEREDITARY PRIMARY MYOPATHY IN THE HOUSE MOUSE.

Authors:  A M Michelson; E S Russell; P J Harman
Journal:  Proc Natl Acad Sci U S A       Date:  1955-12-15       Impact factor: 11.205

4.  A phase-electron microscopic study of extraocular muscle dystrophy in the mouse.

Authors:  B R Pachter; J Davidowitz; G M Breinin
Journal:  Invest Ophthalmol       Date:  1972-09

5.  Abnormalities of peripheral nerves in murine muscular dystrophy.

Authors:  W G Bradley; M Jenkison
Journal:  J Neurol Sci       Date:  1973-02       Impact factor: 3.181

6.  Altered neural protein in murine muscular dystrophy.

Authors:  B Salafsky; C A Stirling
Journal:  Nat New Biol       Date:  1973-11-28

7.  Chimaera mouse study shows absence of disease in genetically dystrophic muscle.

Authors:  A C Peterson
Journal:  Nature       Date:  1974-04-12       Impact factor: 49.962

8.  Functional studies of reeenerated muscles from normal and dystrophic mice.

Authors:  B Salafsky
Journal:  Nature       Date:  1971-01-22       Impact factor: 49.962

9.  Changes in extracellular potassium concentration produced by neuronal activity in the central nervous system of the leech.

Authors:  D A Baylor; J G Nicholls
Journal:  J Physiol       Date:  1969-08       Impact factor: 5.182

10.  A phase and electron microscopic study of dystrophic muscle. I. The pathological changes in the two-week-old Bar Harbor 129 dystrophic mouse.

Authors:  B Q Banker
Journal:  J Neuropathol Exp Neurol       Date:  1967-04       Impact factor: 3.685

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  30 in total

1.  Investigation of cranial and other nerves in the mouse with muscular dystrophy.

Authors:  T J Biscoe; K W Caddy; D J Pallot; U M Pehrson
Journal:  J Neurol Neurosurg Psychiatry       Date:  1975-04       Impact factor: 10.154

Review 2.  Laminins in peripheral nerve development and muscular dystrophy.

Authors:  Wei-Ming Yu; Huaxu Yu; Zu-Lin Chen
Journal:  Mol Neurobiol       Date:  2007-06       Impact factor: 5.590

3.  Cholesterol alterations in young dystrophic mice.

Authors:  D M Logan; K H Tsang
Journal:  Mol Cell Biochem       Date:  1992-03-04       Impact factor: 3.396

Review 4.  Glia unglued: how signals from the extracellular matrix regulate the development of myelinating glia.

Authors:  Holly Colognato; Iva D Tzvetanova
Journal:  Dev Neurobiol       Date:  2011-11       Impact factor: 3.964

5.  Clustering of voltage-sensitive sodium channels on axons is independent of direct Schwann cell contact in the dystrophic mouse.

Authors:  T J Deerinck; S R Levinson; G V Bennett; M H Ellisman
Journal:  J Neurosci       Date:  1997-07-01       Impact factor: 6.167

6.  The structure and composition of peripheral nerves and nerve roots in the Sprawling mouse.

Authors:  L W Duchen; F Scaravilli
Journal:  J Anat       Date:  1977-07       Impact factor: 2.610

7.  Merosin-deficient congenital muscular dystrophy. Partial genetic correction in two mouse models.

Authors:  W Kuang; H Xu; P H Vachon; L Liu; F Loechel; U M Wewer; E Engvall
Journal:  J Clin Invest       Date:  1998-08-15       Impact factor: 14.808

Review 8.  Biological role of dystroglycan in Schwann cell function and its implications in peripheral nervous system diseases.

Authors:  Toshihiro Masaki; Kiichiro Matsumura
Journal:  J Biomed Biotechnol       Date:  2010-06-15

Review 9.  Developmental and pathogenic mechanisms of basement membrane assembly.

Authors:  Peter D Yurchenco; Bruce L Patton
Journal:  Curr Pharm Des       Date:  2009       Impact factor: 3.116

10.  Ephaptic transmission between single nerve fibres in the spinal nerve roots of dystrophic mice.

Authors:  M Rasminsky
Journal:  J Physiol       Date:  1980-08       Impact factor: 5.182

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