| Literature DB >> 31749032 |
Wei Gu1, Dalin Wen2,3, Hongxiang Lu3, Anqiang Zhang3, Haiyan Wang3, Juan Du3, Ling Zeng3, Jianxin Jiang4.
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.Entities:
Keywords: ELANE; Sepsis; miR-608; microRNAs; microarray
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Year: 2019 PMID: 31749032 DOI: 10.1007/s10875-019-00702-8
Source DB: PubMed Journal: J Clin Immunol ISSN: 0271-9142 Impact factor: 8.317