AI Article Synopsis

  • - The study analyzed whole-blood samples from 8 individuals with acute optic neuritis (ON) and 6 healthy controls to identify differences in gene expression using DNA microarrays, revealing 722 differentially expressed genes.
  • - Results showed 377 genes had increased expression and 345 had decreased expression, with key pathways related to protein phosphorylation, apoptosis inhibition, and T/B cell functions implicated in ON pathology.
  • - Quantitative RT-PCR confirmed significant differential expression in 8 selected genes, emphasizing the roles of T cell regulation and anti-inflammatory pathways in the early stages of multiple sclerosis (MS).

Article Abstract

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 , , and 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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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10452153PMC
http://dx.doi.org/10.3390/biomedicines11082209DOI Listing

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