Literature DB >> 1185244

Quantitative ultrastructural studies of the axon Schwann cell abnormality in spinal nerve roots from dystrophic mice.

G M Bray, A J Aguayo.   

Abstract

Lumbo-sacral spinal roots and the nerve to the medial gastrocnemius muscle (NMG) from normal and dystrophic mice were examined by quantitative ultrastructural techniques. It was demonstrated that, although many axons at this level were totally devoid of Schwann cells, totatl axonal numbers were approximately normal. Some axons in these roots were surrounded by Schwann cells but their myelin sheaths were abnormally thin. In addition, cells resembling oligodendrocytes were observed in the dorsal roots of the dystrophic mice. In contrast, Schwann cells and myelin sheaths were normal in the more peripherally situated NMG and the regenerative response of these nerves to crush injury was not significantly different from that of control nerves. Thus, the main abnormality of neural morphology in dystrophic mice is a localized absence of Schwann cells. Such a deficiency does not appear to have influenced axonal growth or the capacity of these axons to regenerate when crushed distally.

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Mesh:

Year:  1975        PMID: 1185244     DOI: 10.1097/00005072-197511000-00006

Source DB:  PubMed          Journal:  J Neuropathol Exp Neurol        ISSN: 0022-3069            Impact factor:   3.685


  9 in total

Review 1.  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

2.  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

3.  Peripheral nerve pathology, including aberrant Schwann cell differentiation, is ameliorated by doxycycline in a laminin-α2-deficient mouse model of congenital muscular dystrophy.

Authors:  Sachiko Homma; Mary Lou Beermann; Jeffrey Boone Miller
Journal:  Hum Mol Genet       Date:  2011-04-19       Impact factor: 6.150

4.  Phospholipid composition and metabolism in mouse muscular dystrophy.

Authors:  C T Kwok; L Austin
Journal:  Biochem J       Date:  1978-10-15       Impact factor: 3.857

5.  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

6.  A quantitative assessment of myelin sheaths in the peripheral nerves of dystrophic, quaking, and trembler mutants.

Authors:  W Beuche; R L Friede
Journal:  Acta Neuropathol       Date:  1985       Impact factor: 17.088

7.  Potassium channel distribution in spinal root axons of dystrophic mice.

Authors:  H Bostock; M Rasminsky
Journal:  J Physiol       Date:  1983-07       Impact factor: 5.182

8.  Transfection of neonatal rat Schwann cells with SV-40 large T antigen gene under control of the metallothionein promoter.

Authors:  G I Tennekoon; J Yoshino; K W Peden; J Bigbee; J L Rutkowski; Y Kishimoto; G H DeVries; G M McKhann
Journal:  J Cell Biol       Date:  1987-11       Impact factor: 10.539

9.  Coordinate control of axon defasciculation and myelination by laminin-2 and -8.

Authors:  Dongren Yang; Jesse Bierman; Yukie S Tarumi; Yong-Ping Zhong; Reshma Rangwala; Thomas M Proctor; Yuko Miyagoe-Suzuki; Shin'ichi Takeda; Jeffrey H Miner; Larry S Sherman; Bruce G Gold; Bruce L Patton
Journal:  J Cell Biol       Date:  2005-02-07       Impact factor: 10.539

  9 in total

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