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Updated: Jul 9, 2026

Cerebrospinal Fluid MicroRNA Profiling Using Quantitative Real Time PCR
Published on: January 22, 2014
セネカバレーウイルス感染IBR S-2細胞から抽出されたエクソソームにおける差次的有意miRNA標的遺伝子解析
Dajun Zhang1, Guowei Xu2, Wenxia Jiang1
1Guangdong Provincial Key Laboratory of Animal Molecular Design and Precise Breeding, School of Animal Science and Technology, Foshan University, Foshan, 528231, China.
Abstract:
Exosomes are nanoscale extracellular vesicles secreted by a wide range of mammalian cells and serve as key mediators in the intercellular transfer of various biological materials such as proteins, nucleic acids, and lipids. However, it remains unclear whether microRNAs (miRNAs) present in exosomes derived from Seneca Valley virus (SVV)-infected swine kidney cells (IBRS-2) undergo substantial alterations. Moreover, the functions and regulatory pathways of differential miRNA target genes involved are unclear. In this study, Exosomes were isolated from SVV-infected IBRS-2 cells and examined for morphology, protein markers, and nucleic acid content using electron microscopy, western blotting, and PCR techniques. Then, the miRNAs present in the exosomes were sequenced, and Gene Ontology (GO) functional annotation along with Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analyses were conducted on the target genes of differentially expressed miRNAs. Consequently, 1419 miRNAs were extracted from exosomes isolated from SVV-infected cells, and the GO functions of 280 differentially expressed miRNAs were related to RNA binding, nucleus, extracellular vesicular exosome, external side of the plasma membrane, cytoplasm, and nucleoplasm. In this research, we present the initial examination of the miRNA expression patterns and the functional roles of their related genes after SVV infects IBRS-2 cells. The results provide important information for investigating the pathogenesis of SVV and developing appropriate therapeutic strategies.
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