PrP 106-126 altered PrP mRNA gene expression in mouse microglia BV-2 cells

Virol Sin. 2010 Dec;25(6):440-4. doi: 10.1007/s12250-010-3143-z. Epub 2011 Jan 10.

Abstract

Prion diseases are infectious and fatal neurodegenerative diseases. The pathogenic agent is an abnormal prion protein aggregate. Microglial activation in the centre nervous system is a characteristic feature of prion disease. In this study, we examined the effect of PrP 106-126 on PrP mRNA gene expression in Mouse microglia cells BV-2 by real-time quantitative PCR. PrP mRNA expression level was found to be significantly increased after 18 h exposure of BV-2 cells to PrP 106-126, with 3-fold increase after 18 h and 4.5-fold increase after 24 h and BV-2 cells proliferating occurred correspondingly. Our results provide the first in vitro evidence of the increase of PrP mRNA levels in microglial cells exposed to PrP 106-126, and indicate that microglial cells might play a critical role in prion pathogenesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Gene Expression*
  • Mice
  • Microglia*
  • Peptide Fragments / biosynthesis*
  • Peptide Fragments / genetics
  • Polymerase Chain Reaction / methods
  • Prions / biosynthesis*
  • Prions / genetics
  • RNA, Messenger / biosynthesis*
  • RNA, Messenger / genetics

Substances

  • Peptide Fragments
  • Prions
  • RNA, Messenger
  • prion protein (106-126)