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PMID: 15992767 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Gene expression profiling of the preclinical scrapie-infected hippocampus.

Biochemical and biophysical research communications ·Vol. 334 ·No. 1 ·2005-08-19 ·Pages 86-95

Brown AR, Rebus S, McKimmie CS, Robertson K, Williams A, Fazakerley JK

Abstract

The molecular events that underlie prion disease neuropathology remain poorly defined. Within the hippocampus of the ME7/CV mouse scrapie model, profound CA1 neuronal loss occurs between 160 and 180 days post-infection (dpi). To elucidate the molecular events that may contribute to this neuronal loss, we have applied Affymetrix high-density oligonucleotide probe arrays to the study of ME7-infected hippocampal gene expression at 170 dpi. The study has identified 78 genes that are differentially expressed greater than 1.5-fold within the preclinical ME7-infected hippocampus prior to the profound late stage glial cell activation. The results indicate oxidative and endoplasmic reticulum (ER) stress, activated ER and mitochondrial apoptosis pathways, and activated cholesterol biosynthesis within the scrapie-infected hippocampus, and offer insight into the molecular events which underlie the neuropathology.

MeSH Terms
Animals Endoplasmic Reticulum/metabolism Gene Expression Profiling/methods Gene Expression Regulation Hippocampus/metabolism Mice Mice, Inbred C57BL Mitochondria/metabolism Nerve Tissue Proteins/metabolism Scrapie/metabolism
Chemicals
Nerve Tissue Proteins
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Brown Alan R
Centre for Infectious Diseases, University of Edinburgh, Edinburgh, Scotland, UK.
Rebus Selma
McKimmie Clive S
Robertson Kevin
Williams Alun
Fazakerley John K
Article Info
Journal
Biochemical and biophysical research communications
Abbr.
Biochem Biophys Res Commun
ISSN
0006-291X
Published
2005-08-19
Pages
86-95
Language
English
Region
United States
NLM ID
0372516
Subset
IM
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