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

First Author  Scaravilli F Year  1981
Journal  Nature Volume  290
Issue  5801 Pages  56-8
PubMed ID  7207584 Mgi Jnum  J:6477
Mgi Id  MGI:54953 Doi  10.1038/290056a0
Citation  Scaravilli F, et al. (1981) Peripheral nerve grafts in hereditary leukodystrophic mutant mice (twitcher). Nature 290(5801):56-8
abstractText  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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