Genome-Wide Expression Profile in People with Optic Neuritis Associated with Multiple Sclerosis

被引:2
|
作者
Habek, Mario [1 ]
Blazekovic, Antonela [2 ,3 ]
Jercic, Kristina Gotovac [2 ,4 ]
Pivac, Nela [5 ]
Outero, Tiago Fleming [6 ,7 ,8 ,9 ]
Borovecki, Fran [2 ,4 ]
Brinar, Vesna [4 ]
机构
[1] Univ Hosp Ctr Zagreb, Referral Ctr Auton Nervous Syst Disorders, Dept Neurol, Zagreb 10000, Croatia
[2] Univ Zagreb, Univ Hosp Ctr Zagreb, Ctr Translat & Clin Res, Dept Funct Genom,Sch Med, Zagreb 10000, Croatia
[3] Univ Zagreb, Dept Anat & Clin Anat, Sch Med, Zagreb 10000, Croatia
[4] Univ Hosp Ctr Zagreb, Dept Neurol, Zagreb 10000, Croatia
[5] Rudjer Boskovic Inst, Div Mol Med, Zagreb 10002, Croatia
[6] Univ Med Ctr Gottingen, Ctr Biostruct Imaging Neurodegenerat, Dept Expt Neurodegenerat, D-37075 Gottingen, Germany
[7] Max Planck Inst Expt Med, D-37075 Gottingen, Germany
[8] Newcastle Univ, Translat & Clin Res Inst, Fac Med Sci, Newcastle Upon Tyne NE1 7RU, England
[9] German Ctr Neurodegenerat Dis DZNE, D-17475 Gottingen, Germany
关键词
optic neuritis; multiple sclerosis; genome-wide expression analysis; GENE-EXPRESSION; ACTIVATION; APOPTOSIS; DIAGNOSIS; DISEASE; CELLS; IL-7;
D O I
10.3390/biomedicines11082209
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 aim of this study was to perform a genome-wide expression analysis of whole-blood samples from people with optic neuritis (ON) and to determine differentially expressed mRNAs compared to healthy control subjects. The study included eight people with acute ON and six healthy control subjects. Gene expression was analyzed using DNA microarrays for whole-human-genome analysis, which contain 54,675 25-base pairs. The additional biostatistical analysis included gene ontology analysis and gene set enrichment analysis (GSEA). Quantitative RT-PCR (qPCR) was used to confirm selected differentially expressed genes. In total, 722 differently expressed genes were identified, with 377 exhibiting increased, and 345 decreased, expression. Gene ontology analysis and GSEA revealed that protein phosphorylation and intracellular compartment, apoptosis inhibition, pathways involved in cell cycles, T and B cell functions, and anti-inflammatory central nervous system (CNS) pathways are implicated in ON pathology. qPCR confirmed the differential expression of eight selected genes, with SLPI, CR3, and ITGA4 exhibiting statistically significant results. In conclusion, whole-blood gene expression analysis showed significant differences in the expression profiles of people with ON compared to healthy control subjects. Additionally, pathways involved in T cell regulation and anti-inflammatory pathways within CNS were identified as important in the early phases of MS.
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页数:12
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