miR-23b Attenuates LPS-Induced Inflammatory Responses in Acute Lung Injury via Inhibition of HDAC2

Biochem Genet. 2021 Apr;59(2):604-616. doi: 10.1007/s10528-020-10018-7. Epub 2021 Jan 7.

Abstract

Inflammatory responses play significant role in infectious etiology-induced acute lung injury (ALI). Histone deacetylase 2 is found to be essential and stimulated in lipopolysaccharide (LPS)-induced ALI by regulating proinflammatory cytokines. miR-23b has been demonstrated to be downregulated in LPS-induced inflammatory injury. In this study, we aimed to explore the interaction between miR-23b and HDAC2 and their function in LPS-induced ALI. LPS treatment was induced on murine alveolar macrophage cell line MH-S. Level of miR-23b and HDAC2 were determined by real-time PCR or Western blot. Proinflammatory cytokines expression and secretion were detected by real-time PCR and ELISA assay. The levels of miR-23b and HDAC2 were manipulated by transient transfection of miRNA mimics, shRNA or overexpression vector. The interaction between miR-23b and HDAC2 were tested by Luciferase reporter assay. LPS treatment inhibited miR-23b expression, while increased HDAC2 level in MH-S cells. Proinflammatory cytokines were stimulated by LPS treatment. Knockdown of HDAC2 or overexpression of miR-23b significantly repressed the expression of proinflammatory cytokines induced by LPS. miR-23b could suppress HDAC2 expression by directly targeting to its mRNA. LPS treatment stimulated the inflammatory responses in macrophages through inhibition of miR-23b, enhanced HDAC2 expression and inducing the expression of its downstream targets TNF-α, IL-6, and IL-1β. Overexpression of miR-23b was sufficient to suppress inflammatory responses by targeting HDAC2, making it a promising therapeutic target to ALI treatment.

Keywords: Acute lung injury; HDAC2; Inflammatory responses; miR-23b.

MeSH terms

  • Acute Lung Injury / chemically induced*
  • Acute Lung Injury / genetics
  • Acute Lung Injury / metabolism*
  • Animals
  • Cell Line
  • Histone Deacetylase 2 / antagonists & inhibitors
  • Histone Deacetylase 2 / genetics
  • Histone Deacetylase 2 / metabolism*
  • Inflammation / chemically induced
  • Inflammation / genetics
  • Inflammation / metabolism
  • Lipopolysaccharides / toxicity*
  • Mice
  • MicroRNAs / genetics
  • MicroRNAs / metabolism*

Substances

  • Lipopolysaccharides
  • MicroRNAs
  • Mirn23b microRNA, mouse
  • HDAC2 protein, human
  • Histone Deacetylase 2