Quercetin alleviates lipopolysaccharide-induced inflammatory responses by up-regulation miR-124 in human renal tubular epithelial cell line HK-2

Biofactors. 2020 May;46(3):402-410. doi: 10.1002/biof.1596. Epub 2019 Dec 5.

Abstract

Chronic kidney disease (CKD) is a persistent kidney structural and functional disorder. Quercetin is one of active extracted flavonoids and has protective effects. Therefore, we proposed to survey the effect of Quercetin on CKD. HK-2 cells were preprocessed by Quercetin and then irritated with lipopolysaccharide (LPS). CCK-8 assay and flow cytometry were utilized to test viability and apoptosis. ELISA assay was utilized to estimate the IL-6 and TNF-α secretion. Western blot was performed to examine the expression of apoptosis and inflammation-associated mediators. After that HK-2 cells were transfected by miR-124 inhibitor. And the above-mentioned parameters were reassessed. LPS stimulated apoptosis and declined viability in HK-2 cells. Additionally, LPS stimulated inflammatory responses. Meanwhile, Quercetin attenuated LPS-stimulated apoptosis, production of IL-6, and TNF-α in experimental cells. Subsequently, MyD88 and miR-124 expression was elevated by LPS and alleviated by Quercetin. Finally, Quercetin exerted its protective function through NF-κB pathway via up-regulating miR-124. Our data demonstrated that Quercetin reduced apoptosis and inflammation stimulated by LPS in HK-2 cells. Moreover, Quercetin alleviated LPS-stimulated injury by up-regulating miR-124.

Keywords: Quercetin; apoptosis; chronic kidney disease; inflammatory responses; miR-124.

Publication types

  • Retracted Publication

MeSH terms

  • Antioxidants / pharmacology
  • Apoptosis / drug effects
  • Cell Survival / drug effects
  • Cells, Cultured
  • Epithelial Cells / drug effects*
  • Humans
  • Inflammation / drug therapy*
  • Inflammation / genetics
  • Kidney Tubules / drug effects*
  • Lipopolysaccharides
  • MicroRNAs / drug effects*
  • MicroRNAs / genetics
  • Quercetin / pharmacology*
  • Up-Regulation / drug effects*
  • Up-Regulation / genetics

Substances

  • Antioxidants
  • Lipopolysaccharides
  • MIRN124 microRNA, human
  • MicroRNAs
  • Quercetin