Gene expression profiling of the preclinical scrapie-infected hippocampus

被引:67
作者
Brown, AR
Rebus, S
McKimmie, CS
Robertson, K
Williams, A
Fazakerley, JK [1 ]
机构
[1] Univ Edinburgh, Ctr Infect Dis, Edinburgh, Midlothian, Scotland
[2] Univ Glasgow, Dept Vet Pathol, Inst Comparat Med, Glasgow, Lanark, Scotland
[3] Univ Edinburgh, Scottish Ctr Genom Technol & Informat, Edinburgh, Midlothian, Scotland
基金
英国生物技术与生命科学研究理事会;
关键词
scrapie; prion disease; gene expression; microarray; endoplasmic reticulum stress; apoptosis; cholesterol; neurodegeneration; hippocampus;
D O I
10.1016/j.bbrc.2005.06.060
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:86 / 95
页数:10
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