Overexpression of TFAM, NRF-1 and myr-AKT protects the MPP(+)-induced mitochondrial dysfunctions in neuronal cells

Biochim Biophys Acta. 2012 May;1820(5):577-85. doi: 10.1016/j.bbagen.2011.08.007. Epub 2011 Aug 11.

Abstract

Background: Mitochondrial dysfunction is a prominent feature of neurodegenerative diseases including Parkinson's disease (PD), in which insulin signaling pathway may also be implicated because 50-80% of PD patients exhibited metabolic syndrome and insulin resistance. 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) and its toxic metabolite, 1-methyl-4-phenyl-2,3-dihydropyridinium ion (MPP(+)), inhibit complex I in mitochondrial respiratory chain and are used widely to construct the PD models. But the precise molecular link between mitochondrial damage and insulin signaling remains unclear.

Methods and results: Using cell-based mitochondrial activity profiling system, we systemically demonstrated that MPP(+) suppressed mitochondrial activity and mitochondrial gene expressions mediated by nuclear respiratory factor-1 (NRF-1) and mitochondrial transcription factor A (TFAM) in SH-SY5Y cells. MPP(+) fragmented mitochondrial networks and repressed phosphorylation of AKT. Similarly, the expressions of mitochondrial genes and tyrosine hydroxylase and AKT phosphorylation were reduced in substantia nigra and striatum of MPTP-injected mice. Transient transfection of TFAM, NRF-1, or myr-AKT reversed all aspects of the MPP(+)-mediated changes.

Conclusions: Mitochondrial activation by TFAM, NRF-1, and myr-AKT abrogated MPP(+)-mediated damages on mitochondria and insulin signaling, leading to recovery of nigrostriatal neurodegeneration.

General significance: We suggest that TFAM, NRF-1, and AKT may be the critical points of therapeutic intervention for PD. This article is part of a Special Issue entitled Biochemistry of Mitochondria.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 1-Methyl-4-phenylpyridinium / toxicity*
  • Animals
  • Apoptosis
  • Blotting, Western
  • Cell Differentiation
  • Cell Line, Tumor
  • Cell Proliferation
  • Corpus Striatum / drug effects
  • Corpus Striatum / metabolism
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism*
  • Female
  • Herbicides / toxicity
  • Humans
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mitochondria / metabolism
  • Mitochondria / pathology*
  • Mitochondrial Proteins / genetics
  • Mitochondrial Proteins / metabolism*
  • NF-E2-Related Factor 1 / genetics
  • NF-E2-Related Factor 1 / metabolism*
  • Neuroblastoma / drug therapy
  • Neuroblastoma / metabolism
  • Neuroblastoma / pathology*
  • Neurons / drug effects
  • Neurons / metabolism
  • Neurons / pathology*
  • Phosphorylation / drug effects
  • Proto-Oncogene Proteins c-akt / genetics
  • Proto-Oncogene Proteins c-akt / metabolism*
  • RNA, Messenger / genetics
  • Rats
  • Rats, Sprague-Dawley
  • Reactive Oxygen Species / metabolism
  • Real-Time Polymerase Chain Reaction
  • Reverse Transcriptase Polymerase Chain Reaction
  • Signal Transduction
  • Substantia Nigra / drug effects
  • Substantia Nigra / metabolism
  • Transcription Factors / genetics
  • Transcription Factors / metabolism*
  • Tyrosine 3-Monooxygenase / metabolism

Substances

  • DNA-Binding Proteins
  • Herbicides
  • Mitochondrial Proteins
  • NF-E2-Related Factor 1
  • RNA, Messenger
  • Reactive Oxygen Species
  • TFAM protein, human
  • Transcription Factors
  • Tyrosine 3-Monooxygenase
  • Proto-Oncogene Proteins c-akt
  • 1-Methyl-4-phenylpyridinium