Back to Search
Start Over
MiR-608 Exerts Anti-inflammatory Effects by Targeting ELANE in Monocytes
- Source :
- Journal of Clinical Immunology. 40:147-157
- Publication Year :
- 2019
- Publisher :
- Springer Science and Business Media LLC, 2019.
-
Abstract
- miR-608 has been indicated to play an important role in the pathogenesis of various inflammation-related diseases, including sepsis and several types of cancers. However, there is little information about the underlying mechanism, especially in inflammatory cells. In this study, an hsa-miR-608-inhibition cell model was constructed in U937 cells using a lentivirus, and gene expression profiles were determined by a cDNA microarray. Altogether, 682 genes showed a difference greater than 1.2-fold, including 184 genes downregulated and 498 genes upregulated. Among these genes, one potential miR-608-target gene, ELANE, was further investigated. A positive relationship between the expression of miR-608 and that of ELANE was found both in vivo and in vitro. In addition, decreased expression of miR-608 resulted in overexpression of ELANE at both the mRNA and protein levels. Cotransfection of HEK293T cells with a miR-608 mimic inhibited reporter activity, and mutation of the miRNA seed sequences abolished the repression of reporter activity. These results suggest that miR-608 is an important posttranscriptional regulator of ELANE expression in human monocytes and may play an important role in the process of inflammation. miR-608 and neutrophil elastase may be novel targets for the diagnosis or treatment of sepsis.
- Subjects :
- 0301 basic medicine
Mutation
biology
U937 cell
Immunology
HEK 293 cells
Inflammation
medicine.disease_cause
03 medical and health sciences
030104 developmental biology
0302 clinical medicine
Neutrophil elastase
Gene expression
microRNA
Cancer research
medicine
biology.protein
Immunology and Allergy
medicine.symptom
Gene
030215 immunology
Subjects
Details
- ISSN :
- 15732592 and 02719142
- Volume :
- 40
- Database :
- OpenAIRE
- Journal :
- Journal of Clinical Immunology
- Accession number :
- edsair.doi...........136cf186af4044b3918ccfd551253434
- Full Text :
- https://doi.org/10.1007/s10875-019-00702-8