Fewer PrPc myeloid-based cells in sheep with the prion-resistant genotype

Neuroreport. 2006 Feb 6;17(2):125-9. doi: 10.1097/01.wnr.0000198430.39691.3c.

Abstract

Numerous sheep with the prion gene (PRNP) that encodes for 171QQ develop scrapie, a neurodegenerative prion disease of sheep. Relatively few cases of scrapie-affected sheep with PRNP genetics that encode for 171RR, however, have been found. Using flow cytometric analysis, statistically fewer PrPc-positive microglia and monocytes were observed from sheep with 171RR PRNP genetics than from sheep with 171QQ PRNP genetics (P<0.05). One possibility for the lack of PrP(Sc) accumulation in brains and lymph nodes of scrapie-exposed sheep with 171RR PRNP genetics is because of fewer PrPc-positive myeloid-derived cells available for conversion of PrPc to PrP(Sc).

Publication types

  • Comparative Study

MeSH terms

  • Animals
  • Animals, Newborn
  • Cells, Cultured
  • Female
  • Flow Cytometry / methods
  • Genotype
  • Glial Fibrillary Acidic Protein / metabolism
  • Immunohistochemistry / methods
  • Microglia / pathology
  • Microglia / ultrastructure
  • Monocytes / metabolism
  • Myeloid Cells / metabolism*
  • Myeloid Cells / ultrastructure
  • Plant Lectins / metabolism
  • PrPC Proteins / metabolism*
  • PrPC Proteins / pathogenicity
  • Prions / genetics*
  • RNA, Messenger / biosynthesis
  • Reverse Transcriptase Polymerase Chain Reaction / methods
  • Scrapie / genetics
  • Scrapie / metabolism*
  • Scrapie / pathology*
  • Sheep

Substances

  • Glial Fibrillary Acidic Protein
  • Plant Lectins
  • PrPC Proteins
  • Prions
  • RNA, Messenger
  • Ricinus communis agglutinin-1