Genome Wide Profiling of Altered Gene Expression in the Neocortex of Alzheimer's Disease

被引:100
|
作者
Tan, Michelle G. [1 ,2 ]
Chua, Wei-Ting [1 ,3 ]
Esiri, Margaret M. [4 ]
Smith, A. David [4 ]
Vinters, Harry V. [5 ,6 ]
Lai, Mitchell K. [1 ,2 ]
机构
[1] Singapore Gen Hosp, Dept Clin Res, Dementia Res Lab, Singapore 169608, Singapore
[2] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Pharmacol, Singapore 117595, Singapore
[3] Nanyang Technol Univ, Sch Biol Sci, Singapore, Singapore
[4] Univ Oxford, John Radcliffe Hosp, OPTIMA, Oxford OX3 9DU, England
[5] Univ Calif Los Angeles, David Geffen Sch Med, Dept Neurol, Sect Neuropathol, Los Angeles, CA 90095 USA
[6] Univ Calif Los Angeles, David Geffen Sch Med, Easton Alzheimer Dis Ctr, Los Angeles, CA 90095 USA
关键词
Alzheimer's Disease; gene expression; microarray; neocortex; neuroinflammation; neurotransmission; synapse; POSTMORTEM HUMAN BRAIN; PROTEIN-KINASE-C; TEMPORAL CORTEX; COGNITIVE IMPAIRMENT; CDNA MICROARRAY; SENILE DEMENTIA; MESSENGER-RNA; UP-REGULATION; RECEPTORS; PATHOLOGY;
D O I
10.1002/jnr.22290
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Alzheimer's disease (AD) is characterized by a complex neurodegenerative process affecting multiple genes and proteins in the neocortex, many of which have not been well-studied. In this study, we investigated genome-wide gene alterations in the temporal cortex of a well-characterized cohort of AD patients using a recently developed microarray platform, and compared some of the transcript changes with immunoblotting. Of the 5485 genes found to be significantly altered in AD, there were consistent patterns of changes which show that the AD transcriptome in neocortex is characterized by changes indicative of synaptic dysfunction, perturbed neurotransmission and activation of neuroinflammation. We also highlighted several genes of potential pathogenic significance which have not been well studied in AD. The current study aims to add to the growing body of knowledge relating to gene changes in AD and provide further insights into pathogenic mechanisms and potential targets of pharmacotherapy. (C) 2009 Wiley-Liss, Inc.
引用
收藏
页码:1157 / 1169
页数:13
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