Transduced Tat-DJ-1 protein inhibits cytokines-induced pancreatic RINm5F cell death

BMB Rep. 2016 May;49(5):297-302. doi: 10.5483/bmbrep.2016.49.5.058.

Abstract

Loss of pancreatic β-cells by oxidative stress or cytokines is associated with diabetes mellitus (DM). DJ-1 is known to as a multifunctional protein, which plays an important role in cell survival. We prepared cell permeable wild type (WT) and mutant type (M26I) Tat-DJ-1 proteins to investigate the effects of DJ-1 against combined cytokines (IL-1β, IFN-γ and TNF-α)-induced RINm5F cell death. Both Tat-DJ-1 proteins were transduced into RINm5F cells. WT Tat-DJ-1 proteins significantly protected against cell death from cytokines by reducing intracellular toxicities. Also, WT Tat-DJ-1 proteins markedly regulated cytokines-induced pro- and anti-apoptosis proteins. However, M26I Tat-DJ-1 protein showed relatively low protective effects, as compared to WT Tat-DJ-1 protein. Our experiments demonstrated that WT Tat-DJ-1 protein protects against cytokine-induced RINm5F cell death by suppressing intracellular toxicities and regulating apoptosisrelated protein expression. Thus, WT Tat-DJ-1 protein could potentially serve as a therapeutic agent for DM and cytokine related diseases. [BMB Reports 2016; 49(5): 297-302].

Publication types

  • News

MeSH terms

  • Animals
  • Cell Death / drug effects
  • Cell Line
  • Cytokines / pharmacology*
  • Humans
  • Pancreas / pathology*
  • Protein Deglycase DJ-1 / metabolism*
  • Rats
  • Recombinant Fusion Proteins / metabolism*
  • Recombinant Fusion Proteins / pharmacology
  • Signal Transduction / drug effects
  • Transduction, Genetic*
  • tat Gene Products, Human Immunodeficiency Virus / metabolism*

Substances

  • Cytokines
  • Recombinant Fusion Proteins
  • tat Gene Products, Human Immunodeficiency Virus
  • Protein Deglycase DJ-1