A mouse prion protein transgene rescues mice deficient for the prion protein gene from purkinje cell degeneration and demyelination

Lab Invest. 1999 Jun;79(6):689-97.

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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3' Untranslated Regions
  • Alleles
  • Animals
  • Brain / pathology*
  • Cricetinae
  • Demyelinating Diseases / genetics*
  • Demyelinating Diseases / physiopathology
  • Demyelinating Diseases / prevention & control
  • Exons
  • Introns
  • Mesocricetus
  • Mice
  • Mice, Mutant Strains
  • Mice, Transgenic
  • Motor Activity
  • Peripheral Nerves / pathology
  • Prions / genetics*
  • Prions / physiology*
  • Psychomotor Performance
  • Purkinje Cells / pathology*
  • Spinal Cord / pathology
  • Vacuoles / pathology

Substances

  • 3' Untranslated Regions
  • Prions