Acceso usuarios
Background and objectives: Accumulating evidence suggests that exosomal miRNAs play important roles in disease pathogenesis; however, their role in the pathogenesis of depression remains largely unknown. We explored the miRNA profile of circulating exosomes in a patient with depression and compared it with a healthy volunteer.
Methods: Serum exosomes were isolated from a patient and volunteer, and exosomal miRNAs were analyzed by miRNA-sequencing. MiRTarbase and gene ontology (GO) analysis were used to predict the downstream signaling pathways of the depression-specific miRNAs.
Results: miRNA-sequencing analysis identified 12 up-regulated miRNAs and 20 down-regulated miRNAs in the depressed patient. MiRTarbase and GO analysis revealed that the up-regulated miRNAs regulated the expression of genes involved in histone/chromatin modification and the neurotrophin signaling pathway. The down-regulated miRNAs regulated genes were associated with apoptosis, hypoxia, cell growth, and immune response.
Conclusions: Depression-specific miRNAs may modulate neurotrophin signaling, chromatin/histone modification, immune system function, inflammation, depression, apoptosis, hypoxia, and cell growth. Identifying the networks that may be regulated by these depressionspecific miRNAs and their target genes may provide a novel, high-throughput screening platform for the early detection of depression as well as determining its severity and response to treatment
