Microarray analysis in Alzheimer's disease and normal aging

被引:68
作者
Ricciarelli, R
d'Abramo, C
Massone, S
Marinari, UM
Pronzato, MA
Tabaton, M
机构
[1] Univ Genoa, Dept Expt Med, I-16132 Genoa, Italy
[2] Univ Genoa, Dept Neurol Sci & Vis, I-16132 Genoa, Italy
关键词
Alzheimer's disease; microarray; aging; interferon-induced; protein; 3; beta amyloid;
D O I
10.1080/15216540412331286002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
The purpose of this study was to investigate gene expression in Alzheimer's disease ( AD), the most common form of senile dementia. We utilized the microarray technology to simultaneously compare the expression pro. le of 12,000 human genes in cerebral cortex of AD and normal aging. To identify gene expression related to neurodegeneration, beside the presence of amyloid deposition, we used control brains with abundant amyloid plaques, derived from cognitively normal elderly subjects. The microarray analysis indicated that 314 genes were differentially expressed in AD cerebral cortex, with differences greater than 5 folds in 25 genes. RT-PCR performed on a selected group of genes confirmed the increased expression of the interferon-induced protein 3 in AD brain. This protein, which is highly inducible by both type I and type II interferons, was not previously associated with the neurodegenerative disease.
引用
收藏
页码:349 / 354
页数:6
相关论文
共 32 条
[1]
Up-regulation of the inflammatory cytokines IFN-γ and IL-12 and down-regulation of IL-4 in cerebral cortex regions of APPSWE transgenic mice [J].
Abbas, N ;
Bednar, I ;
Mix, E ;
Marie, S ;
Paterson, D ;
Ljungberg, A ;
Morris, C ;
Winblad, B ;
Nordberg, A ;
Zhu, J .
JOURNAL OF NEUROIMMUNOLOGY, 2002, 126 (1-2) :50-57
[2]
Both aging and chronic fluoxetine increase S100B content in the mouse hippocampus [J].
Akhisaroglu, M ;
Manev, R ;
Akhisaroglu, E ;
Uz, T ;
Manev, H .
NEUROREPORT, 2003, 14 (11) :1471-1473
[3]
Protein oxidation in the brain in Alzheimer's disease [J].
Aksenov, MY ;
Aksenova, MV ;
Butterfield, DA ;
Geddes, JW ;
Markesbery, WR .
NEUROSCIENCE, 2001, 103 (02) :373-383
[4]
Alzheimer's disease and the basal forebrain cholinergic system:: relations to β-amyloid peptides, cognition, and treatment strategies [J].
Auld, DS ;
Kornecook, TJ ;
Bastianetto, S ;
Quirion, R .
PROGRESS IN NEUROBIOLOGY, 2002, 68 (03) :209-245
[5]
Antioxidant-rich diets improve cerebellar physiology and motor learning in aged rats [J].
Bickford, PC ;
Gould, T ;
Briederick, L ;
Chadman, K ;
Pollock, A ;
Young, D ;
Shukitt-Hale, B ;
Joseph, J .
BRAIN RESEARCH, 2000, 866 (1-2) :211-217
[6]
Convergence of atherosclerosis and Alzheimer's disease: inflammation, cholesterol, and misfolded proteins [J].
Casserly, I ;
Topol, E .
LANCET, 2004, 363 (9415) :1139-1146
[7]
Gene expression profiling of 12633 genes in Alzheimer hippocampal CA1: Transcription and neurotrophic factor down-regulation and up-regulation of apoptotic and pro-inflammatory signaling [J].
Colangelo, V ;
Schurr, J ;
Ball, MJ ;
Pelaez, RP ;
Bazan, NG ;
Lukiw, WJ .
JOURNAL OF NEUROSCIENCE RESEARCH, 2002, 70 (03) :462-473
[8]
'Unfolding' pathways in neurodegenerative disease [J].
Forman, MS ;
Lee, VMY ;
Trojanowski, JQ .
TRENDS IN NEUROSCIENCES, 2003, 26 (08) :407-410
[9]
Interactions of oxidative stress with cellular calcium dynamics and glucose metabolism in Alzheimer's disease [J].
Gibson, GE .
FREE RADICAL BIOLOGY AND MEDICINE, 2002, 32 (11) :1061-1070
[10]
Ginsberg SD, 2000, ANN NEUROL, V48, P77, DOI 10.1002/1531-8249(200007)48:1<77::AID-ANA12>3.3.CO