| Literature DB >> 10378511 |
N Nishida1, P Tremblay, T Sugimoto, K Shigematsu, S Shirabe, C Petromilli, S P Erpel, R Nakaoke, R Atarashi, T Houtani, M Torchia, S Sakaguchi, S J DeArmond, S B Prusiner, S Katamine.
Abstract
Disruption of both alleles of the prion protein gene, Prnp, renders mice resistant to prions; in a Prnp o/o line reported by some of us, mice progressively developed ataxia and Purkinje cell loss. Here we report torpedo-like axonal swellings associated with residual Purkinje cells in Prnp o/o mice, and we demonstrate abnormal myelination in the spinal cord and peripheral nerves in mice from two independently established Prnp o/o lines. Mice were successfully rescued from both demyelination and Purkinje cell degeneration by introduction of a transgene encoding wild-type mouse cellular prion protein. These findings suggest that cellular prion protein expression may be necessary to maintain the integrity of the nervous system.Entities:
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Year: 1999 PMID: 10378511
Source DB: PubMed Journal: Lab Invest ISSN: 0023-6837 Impact factor: 5.662