BAG5 protects against mitochondrial oxidative damage through regulating PINK1 degradation

PLoS One. 2014 Jan 24;9(1):e86276. doi: 10.1371/journal.pone.0086276. eCollection 2014.

Abstract

Mutations in PTEN-induced kinase 1 (PINK1) gene cause PARK6 familial Parkinsonism, and loss of the stability of PINK1 may also contribute to sporadic Parkinson's disease (PD). Degradation of PINK1 occurs predominantly through the ubiquitin proteasome system (UPS), however, to date, few of the proteins have been found to regulate the degradation of PINK1. Using the yeast two-hybrid system and pull-down methods, we identified bcl-2-associated athanogene 5 (BAG5), a BAG family member, directly interacted with PINK1. We showed that BAG5 stabilized PINK1 by decreasing the ubiquitination of PINK1. Interestingly, BAG5 rescued MPP(+)- and rotenone-induced mitochondria dysfunction by up-regulating PINK1 in vitro. In PINK1-null mice and MPTP-treated mice, BAG5 significantly increased in the substantia nigra pars compacta (SNpc) although PINK1 was decreased. Our findings indicated that BAG5, as a key protein to stabilize PINK1, is a promising therapeutic tool for preventing mitochondrial dysfunction following oxidative stress.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine / pharmacology
  • Adaptor Proteins, Signal Transducing / genetics*
  • Adaptor Proteins, Signal Transducing / metabolism*
  • Animals
  • Cell Line
  • Humans
  • Mice
  • Mitochondria / drug effects
  • Mitochondria / genetics*
  • Mitochondria / metabolism*
  • Neurotoxins / toxicity
  • Oxidative Stress*
  • Protein Binding
  • Protein Kinases / genetics
  • Protein Kinases / metabolism*
  • Protein Stability
  • Proteolysis
  • Rotenone / pharmacology
  • Substantia Nigra / drug effects
  • Substantia Nigra / metabolism
  • Ubiquitination

Substances

  • Adaptor Proteins, Signal Transducing
  • BAG5 protein, human
  • Neurotoxins
  • Rotenone
  • 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine
  • Protein Kinases
  • PTEN-induced putative kinase

Grants and funding

This work was supported by grant from the Major State Basic Research Development Program of China (973 Program) (2011CB510000), grant from the National Natural Science Foundation of China(30900469,81171198, 81200870, 81000542, 81130021, 81371405, 81361120404). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.