Prion proteins from susceptible and resistant sheep exhibit some distinct cell biological features

Biochem Biophys Res Commun. 2005 Nov 25;337(3):791-8. doi: 10.1016/j.bbrc.2005.09.114. Epub 2005 Sep 28.

Abstract

It is well established that natural polymorphisms in the coding sequence of the PrP protein can control the expression of prion disease. Studies with a cell model of sheep prion infection have shown that ovine PrP allele associated with resistance to sheep scrapie may confer resistance by impairing the multiplication of the infectious agent. To further explore the biochemical and cellular mechanisms underlying the genetic control of scrapie susceptibility, we established permissive cells expressing two different PrP variants. In this study, we show that PrP variants with opposite effects on prion multiplication exhibit distinct cell biological features. These findings indicate that cell biological properties of ovine PrP can vary with natural polymorphisms and raise the possibility that differential interactions of PrP variants with the cellular machinery may contribute to permissiveness or resistance to prion multiplication.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Cells, Cultured
  • Disease Susceptibility / physiopathology*
  • Epithelial Cells / chemistry*
  • Epithelial Cells / metabolism*
  • Epithelial Cells / pathology
  • Immunity, Innate / physiology*
  • Molecular Sequence Data
  • Prions / analysis
  • Prions / chemistry*
  • Prions / metabolism*
  • Protein Transport*
  • Sheep
  • Structure-Activity Relationship

Substances

  • Prions