MBD2 upregulates miR-301a-5p to induce kidney cell apoptosis during vancomycin-induced AKI

Cell Death Dis. 2017 Oct 12;8(10):e3120. doi: 10.1038/cddis.2017.509.

Abstract

Despite DNA methylation occurred in acute kidney injury (AKI), how it influenced progression of AKI remains unclear. Methyl-CpG-binding domain protein 2 (MBD2), a protein readers of methylation, was used to analyze the impact of DNA methylation on vancomycin (VAN)-induced AKI. Here, in cultured human kidney tubular epithelial cells (HK-2), we show that knockdown of MBD2 by siRNA attenuated VAN-induced apoptosis, caspase activity, and the expression of BAX and cleaved caspase 3. Interestingly, knockdown of MBD2 by siRNA was associated with the suppression of miR-301a-5p. Mechanistic studies confirmed MBD2 binds to these methylated CpG elements of miR-301a-5p promoter, and then activates miR-301a-5p promoter by suppressing methylation. Furthermore, anti-miR-301a-5p significantly blocked VAN-induced apoptosis and caspase activity in HK-2 cells, which was accompanied by downregulation of p53, and upregulation of MITF, HDGF and MDM-4 together. The latter genes were further identified as target genes of miR-301a-5p, and silencing of MDM-4 promoted p53 accumulation. In vivo, mice with MBD2 knockout (MBD2-KO) were counteracted to VAN-induced AKI, indicated by the analysis of renal function, histology, apoptosis and inflammation. MBD2-KO also significantly suppressed the expression of miR-301a-5p, p53, BAX and cleaved caspase 3, and restored the expression of MDM-4, MITF and HDGF. Finally, in vivo inhibition of miR-301a-5p also ameliorated VAN-induced AKI. Together, these results show the novel MBD2/miR-301a-5p/MITF, HDGF and MDM-4/p53 pathway in VAN-induced AKI.

MeSH terms

  • Acute Kidney Injury / chemically induced
  • Acute Kidney Injury / genetics
  • Acute Kidney Injury / metabolism
  • Acute Kidney Injury / prevention & control*
  • Animals
  • Apoptosis / genetics*
  • Caspase 3 / metabolism
  • Cell Cycle Proteins
  • Cell Line, Transformed
  • CpG Islands / genetics
  • Cytoskeletal Proteins
  • DNA Methylation / genetics
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism*
  • Gene Expression Regulation / genetics
  • Humans
  • In Situ Nick-End Labeling
  • Intracellular Signaling Peptides and Proteins
  • Kidney / cytology
  • Kidney / metabolism
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • MicroRNAs / biosynthesis
  • MicroRNAs / genetics*
  • Microphthalmia-Associated Transcription Factor / biosynthesis
  • Nuclear Proteins / biosynthesis*
  • Promoter Regions, Genetic / genetics
  • Proto-Oncogene Proteins / biosynthesis*
  • RNA Interference
  • RNA, Small Interfering / genetics
  • Tumor Suppressor Protein p53 / metabolism
  • Vancomycin / toxicity*
  • bcl-2-Associated X Protein / biosynthesis

Substances

  • BAX protein, human
  • Cell Cycle Proteins
  • Cytoskeletal Proteins
  • DNA-Binding Proteins
  • HDGFL3 protein, human
  • Intracellular Signaling Peptides and Proteins
  • MBD2 protein, human
  • MDM4 protein, human
  • MIRN301A microRNA, human
  • MITF protein, human
  • MicroRNAs
  • Microphthalmia-Associated Transcription Factor
  • Nuclear Proteins
  • Proto-Oncogene Proteins
  • RNA, Small Interfering
  • TP53 protein, human
  • Tumor Suppressor Protein p53
  • bcl-2-Associated X Protein
  • Vancomycin
  • Caspase 3