Zinc supplementation alleviates OTA-induced oxidative stress and apoptosis in MDCK cells by up-regulating metallothioneins

Life Sci. 2019 Oct 1:234:116735. doi: 10.1016/j.lfs.2019.116735. Epub 2019 Aug 5.

Abstract

Aims: The present study was to investigate the protective effects of Zn supplementation in OTA-induced apoptosis of Madin-Darby canine kidney (MDCK) epithelial cells and explore the potential mechanisms. Aiming to provides a new insight into the treatment strategy of OTA-induced nephrotoxicity by nutritional regulation.

Main methods: Initially, through MTT and LDH assay revealed that Zn supplementation significantly suppressed OTA-induced cytotoxicity in MDCK cells. Then, the production of reactive oxygen species (ROS) was detected by using a DCFH-DA assay. Annexin V-FITC/PI, Hoechst 33258 staining and Flow cytometry were used to detect the apoptosis. The expressions of apoptosis-related molecules were determined by RT-PCR, Western blotting. Interestingly, OTA treatment slightly increased the levels of Metallothionein-1 (MT-1) and Metallothionein-2 (MT-2) by using RT-PCR, Western blotting assay; while Zn supplementation further improved the increase of MT-1 and MT-2 induced by OTA. However, the inhibitive effects of Zn supplementation were significantly blocked after double knockdown of MT-1 and MT-2 by using Small Interfering RNA (siRNA) Transfection method.

Key findings: Our study provides supportive data for the potential roles of Zn in reducing OTA-induced oxidative stress and apoptosis in MDCK cells.

Significance: Zn is one of the key structural components of many proteins, which plays an important role in several physiological processes such as cell survival and apoptosis. This metal is expected to contribute to the conservative and adjuvant treatment of kidney disease and should therefore be investigated further.

Keywords: Apoptosis; MDCK cells; Metallothioneins; Ochratoxin A; Zinc.

MeSH terms

  • Animals
  • Apoptosis / drug effects*
  • Cytoprotection / drug effects
  • Dogs
  • Epithelial Cells / cytology
  • Epithelial Cells / drug effects*
  • Epithelial Cells / metabolism
  • Madin Darby Canine Kidney Cells
  • Metallothionein / genetics*
  • Ochratoxins / toxicity*
  • Oxidative Stress / drug effects
  • Protective Agents / pharmacology*
  • Up-Regulation / drug effects
  • Zinc / pharmacology*

Substances

  • Ochratoxins
  • Protective Agents
  • ochratoxin A
  • Metallothionein
  • Zinc