Exploitation of microRNAs by Japanese Encephalitis virus in human microglial cells.
Meghana RastogiNeha SrivastavaSunit Kumar SinghPublished in: Journal of medical virology (2017)
JEV infection in CNS leads to the JE neuroinflammation. Children and old age individual have been reported to be more prone to JEV infection. MicroRNAs are endogenous, small non-coding RNAs, which regulate the gene expression. These are ∼22 nucleotide long, conserved RNA sequence that binds at the 3'UTR of a target mRNA and regulate the post-transcriptional gene expression. The role of microRNAs has been reported in several diseases like cancer, viral infection, neuro-degeneration, diabetes etc. In the present study, the human microglial cells were infected with JEV (JaOArS982). The control and infected samples were subject to microarray profiling for microRNA expression. The microarray profile yielded differentially expressed microRNAs from JEV infected samples. The microRNA gene targets, gene ontology, annotations, and pathways were identified through various bioinformatics tools. Additionally, the pathways were mostly found common to "ubiquitin mediated proteolysis," "cytokine signaling," "maintenance of barrier function/cell junctions," JAK/STAT pathway" "Toll-like receptor signaling," "Wnt-signaling," "adhesion molecules," "apoptosis," "endocytosis," "vesicle mediated transport" etc.
Keyphrases
- gene expression
- cell cycle arrest
- toll like receptor
- induced apoptosis
- inflammatory response
- endothelial cells
- lipopolysaccharide induced
- dna methylation
- endoplasmic reticulum stress
- cell death
- lps induced
- oxidative stress
- single cell
- copy number
- poor prognosis
- transcription factor
- induced pluripotent stem cells
- pi k akt
- cardiovascular disease
- genome wide
- type diabetes
- binding protein
- signaling pathway
- pluripotent stem cells
- traumatic brain injury
- squamous cell carcinoma
- cell therapy
- cystic fibrosis
- cognitive impairment
- cell proliferation
- neuropathic pain
- biofilm formation
- heat shock
- blood brain barrier
- genome wide identification
- metabolic syndrome
- insulin resistance
- squamous cell
- staphylococcus aureus
- heat stress