Gene expression profiling in multiple sclerosis: A disease of the central nervous system, but with relapses triggered in the periphery?

被引:41
作者
Brynedal, Boel [1 ]
Khademi, Mohsen [2 ]
Wallstrom, Erik [2 ]
Hillert, Jan [1 ]
Olsson, Tomas [2 ]
Duvefelt, Kristina [3 ]
机构
[1] Karolinska Inst, Dept Clin Neurosci, Ctr Mol Med, Multiple Sclerosis Res Grp, S-17176 Stockholm, Sweden
[2] Karolinska Inst, Clin Neurosci, Ctr Mol Med, Neuroimmunol Unit, S-17176 Stockholm, Sweden
[3] Karolinska Univ Hosp, Clin Res Ctr, Mutat Anal Facil, Stockholm, Sweden
基金
瑞典研究理事会;
关键词
Gene expression profiling; Microarray; Multiple sclerosis; Relapse; CSF; PBMC; EXPERIMENTAL ALLERGIC ENCEPHALOMYELITIS; KAPPA-B; BIOCONDUCTOR; IDENTIFICATION; TRANSCRIPTOME; ACTIVATION; DATABASE; GENOMES; CELLS; MODEL;
D O I
10.1016/j.nbd.2009.11.014
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The aetiology of multiple sclerosis (MS), an autoimmune demyelinating disease of the central nervous system (CNS), includes both genetic and environmental factors, but the pathogenesis is still incompletely known. We performed gene expression profiling on paired cerebrospinal fluid (CSF) and peripheral blood mononuclear cells (PBMCs) samples from 26 MS patients without immunomodulatory treatment, sampled in relapse or remission, and 18 controls using Human Genome U133 plus 2.0 arrays (Affymetrix). In the CSF, 939 probe sets detected differential expression in MS patients compared to controls, but none in PBMCs, confirming that CSF cells might mirror the disease processes. The regulation of selected transcripts in CSF of MS patients was confirmed by quantitative PCR. Unexpectedly however, when comparing MS patients in relapse to those in remission, 266 probe sets detected differential expression in PBMCs, but not in CSF cells, indicating the importance of events outside of the CNS in the triggering of relapse. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:613 / 621
页数:9
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