Microarray detection of E2F pathway activation and other targets in multiple sclerosis peripheral blood mononuclear cells

被引:56
作者
Iglesias, AH
Camelo, S
Hwang, DH
Villanueva, R
Stephanopoulos, G
Dangond, F
机构
[1] Harvard Univ, Sch Med, Dept Neurol, Brigham & Womens Hosp,Lab Transcript & Immune Reg, Boston, MA USA
[2] MIT, Dept Chem Engn, Bioinformat & Metab Engn Lab, Cambridge, MA 02139 USA
关键词
multiple sclerosis; DNA microarrays; gene expression; experimental autoimmune encephalomyelitis; autoimmunity;
D O I
10.1016/j.jneuroim.2004.01.017
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We performed microarray analysis of peripheral blood mononuclear cells (PBMCs) from multiple sclerosis (MS) patients and detected a profile of immune cell activation, autoantigen upregulation, and enhanced E2F pathway transcription. Accordingly, E2fl-deficient mice manifested only mild disability upon induction of experimental autoimmune encephalomyelitis (EAE). Furthermore, PBMCs from Avonex-treated patients had lower expression of E2F targets. The profile was enriched in genes known to harbor MS-associated polymorphisms, or localized to MS susceptibility chromosomal regions. Our study shows that PBMC microarrays reflect MS pathobiology that can be validated in the EAE model. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:163 / 177
页数:15
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