AI Article Synopsis

  • The study investigates miRNA-155 expression in the livers of mice suffering from LPS-induced sepsis and the effects of dexamethasone (DXM) on this expression.
  • Results showed that miRNA-155 and inflammatory factors increased in the liver due to sepsis, while DXM reduced miRNA-155 levels in a dose-dependent way, but did not affect inflammatory factors significantly.
  • The findings suggest that elevated miRNA-155 may contribute to sepsis pathology and that DXM may regulate inflammation through its effects on miRNA-155 expression.

Article Abstract

To investigate the expression of microRNA-155 (miRNA-155) in the livers of mice with lipopolysaccharide (LPS)-induced sepsis and to determine the role of dexamethasone (DXM) in the regulation of miRNA-155 expression, we pretreated mice with or without DXM prior to LPS exposure. Our study demonstrated that the expression of miRNA-155 and inflammatory factors increased in the liver tissues of mice with LPS-induced sepsis and that DXM down-regulated their expression in a dose-dependent manner. Moreover, DXM alone inhibited the expression of miRNA-155 to below the baseline level, but did not impact the expression of inflammatory factors, suggesting that the down-regulation of miRNA-155 by DXM may partially, but not completely, depend on the suppression of pro-inflammatory cytokines by DXM. Our data indicate that the overexpression of miRNA-155 in the livers of mice with LPS-induced sepsis may play an important role in the pathological processes of sepsis and that the down-regulation of miRNA-155 by DXM may be a novel mechanism regulating inflammation and immunity.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3823654PMC
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0080547PLOS

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