Literature DB >> 7207584

Peripheral nerve grafts in hereditary leukodystrophic mutant mice (twitcher).

F Scaravilli, J M Jacobs.   

Abstract

The twitcher mouse is a mutant affected by a form of leukodystrophy which shows close similarities to human globoid cell (Krabbe's) leukodystrophy. Transmission is by an autosomal recessive gene twi. Progressive loss of myelin sheaths from both central and peripheral nervous systems and the presence of inclusion-laden macrophages are characteristic findings. Morphological features of the twitcher have been described by Duchen et al. Nerve iso- and allografting have been used to determine the roles of axon and Schwann cell in a number of mouse and human nerve abnormalities. Schwann cells in a graft proliferate and become associated with regenerating host axons which grow through the graft into the host distal stump. In the twitcher, peripheral nerve axons do not degenerate but are thinner than normal, although there is considerable axonal degeneration in the central nervous system. In 15-day-old mutants, inclusions have been found in Schwann cells associated with apparently normal myelin sheaths. Grafting experiments might show whether the phenotype of this mutant is fully expressed in the Schwann cell, or if axons are also involved. In previous experiments, survival of transplanted Schwann cells was achieved by the use of T cell-suppressed or nude mice. We report here that a twitcher nerve transplanted in immunologically unsuppressed animals reproduces all the characteristic features of leukodystrophy and conversely that Schwann cells from unaffected mice can produce normal myelin when associated with twitcher axons.

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Year:  1981        PMID: 7207584     DOI: 10.1038/290056a0

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  5 in total

1.  Defective Schwann cell function in canine inherited hypertrophic neuropathy.

Authors:  B J Cooper; I Duncan; J Cummings; A de Lahunta
Journal:  Acta Neuropathol       Date:  1984       Impact factor: 17.088

2.  The twitcher mouse. A model of human globoid cell leukodystrophy (krabbe's disease).

Authors:  K Suzuki; K Suzuki
Journal:  Am J Pathol       Date:  1983-06       Impact factor: 4.307

3.  Disorders in myelination in the twitcher mutant: immunohistochemical and biochemical studies.

Authors:  K Mikoshiba; M Fujishiro; S Kohsaka; H Okano; K Takamatsu; Y Tsukada
Journal:  Neurochem Res       Date:  1985-08       Impact factor: 3.996

4.  Molecular beacon genotyping for globoid cell leukodystrophy from hair roots in the twitcher mouse and rhesus macaque.

Authors:  Kimberly A Terrell; Terri A Rasmussen; Cyndi Trygg; Bruce A Bunnell; Wayne R Buck
Journal:  J Neurosci Methods       Date:  2007-02-25       Impact factor: 2.390

Review 5.  Pre-clinical Mouse Models of Neurodegenerative Lysosomal Storage Diseases.

Authors:  Jacob M Favret; Nadav I Weinstock; M Laura Feltri; Daesung Shin
Journal:  Front Mol Biosci       Date:  2020-04-15
  5 in total

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