PARP-1 overexpression contributes to Cadmium-induced death in rat proximal tubular cells via parthanatos and the MAPK signalling pathway

Sci Rep. 2017 Jun 28;7(1):4331. doi: 10.1038/s41598-017-04555-2.

Abstract

Parthanatos is a newly discovered form of PARP-1-dependent programmed cell death. It has been reported to play an important role in several cancer or tumour cells; however, few studies have been performed in normal cells. Cadmium is a highly toxic pollutant and is reported to induce autophagy and apoptosis in multiple cell types. Although cadmium toxicity induces cell death, the underlying mechanism is not fully understood. Therefore, in this study we aimed to investigate the mechanism of Cadmium -induced cell damage using rat proximal tubular cell line NRK-52E and primary rat proximal tubular (rPT) cells. Our results indicated that parthanatos and the MAPK signalling pathway contribute to Cadmium-induced cell death, and that oxidative stress and mitochondrial damage play key roles in this process. In addition, parthanatos with oxidative stress has a synergistic effect on apoptosis, and JNK1/2 and p38 contribute to parthanatos.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphate / metabolism
  • Animals
  • Apoptosis / drug effects
  • Cadmium / toxicity*
  • Cell Line
  • Cell Proliferation / drug effects
  • Cell Survival / drug effects
  • Environmental Pollutants / adverse effects
  • Epithelial Cells / drug effects*
  • Epithelial Cells / metabolism*
  • Gene Expression*
  • Kidney Tubules, Proximal / metabolism*
  • MAP Kinase Signaling System / drug effects*
  • Mitochondria / drug effects
  • NAD / metabolism
  • Oxidative Stress / drug effects
  • Poly (ADP-Ribose) Polymerase-1 / genetics*
  • Rats
  • Reactive Oxygen Species / metabolism

Substances

  • Environmental Pollutants
  • Reactive Oxygen Species
  • Cadmium
  • NAD
  • Adenosine Triphosphate
  • Parp1 protein, rat
  • Poly (ADP-Ribose) Polymerase-1