The Nrf2/SKN-1-dependent glutathione S-transferase π homologue GST-1 inhibits dopamine neuron degeneration in a Caenorhabditis elegans model of manganism

Raja Settivari, Natalia VanDuyn, Jennifer LeVora, Richard Nass

Research output: Contribution to journalArticle

26 Citations (Scopus)

Abstract

Exposure to high levels of manganese (Mn) results in a neurological condition termed manganism, which is characterized by oxidative stress, abnormal dopamine (DA) signaling, and cell death. Epidemiological evidence suggests correlations with occupational exposure to Mn and the development of the movement disorder Parkinson's disease (PD), yet the molecular determinants common between the diseases are ill-defined. Glutathione S-transferases (GSTs) of the class pi (GSTπ) are phase II detoxification enzymes that conjugate both endogenous and exogenous compounds to glutathione to reduce cellular oxidative stress, and their decreased expression has recently been implicated in PD progression. In this study we demonstrate that a Caenorhabditis elegans GSTπ homologue, GST-1, inhibits Mn-induced DA neuron degeneration. We show that GST-1 is expressed in DA neurons, Mn induces GST-1 gene and protein expression, and GST-1-mediated neuroprotection is dependent on the PD-associated transcription factor Nrf2/SKN-1, as a reduction in SKN-1 gene expression results in a decrease in GST-1 protein expression and an increase in DA neuronal death. Furthermore, decreases in gene expression of the SKN-1 inhibitor WDR-23 or the GSTπ-binding cell death activator JNK/JNK-1 result in an increase in resistance to the metal. Finally, we show that the Mn-induced DA neuron degeneration is independent of the dopamine transporter DAT, but is largely dependent on the caspases CED-3 and the novel caspase CSP-1. This study identifies a C. elegans Nrf2/SKN-1-dependent GSTπ homologue, cell death effectors of GSTπ-associated xenobiotic-induced pathology, and provides the first in vivo evidence that a phase II detoxification enzyme may modulate DA neuron vulnerability in manganism.

Original languageEnglish
Pages (from-to)51-60
Number of pages10
JournalNeuroToxicology
Volume38
DOIs
StatePublished - Sep 2013

Fingerprint

Nerve Degeneration
Dopaminergic Neurons
Caenorhabditis elegans
Glutathione Transferase
Neurons
Dopamine
Manganese
Phase II Metabolic Detoxication
Cell death
Parkinson Disease
Cell Death
Detoxification
Oxidative stress
Gene Expression
Caspases
Gene expression
Oxidative Stress
Glutathione S-Transferase pi
Caspase 1
Dopamine Plasma Membrane Transport Proteins

Keywords

  • Caspase
  • Manganism
  • Neurodegeneration
  • Neurotoxicity
  • Nrf2
  • Parkinson's disease

ASJC Scopus subject areas

  • Neuroscience(all)
  • Toxicology

Cite this

The Nrf2/SKN-1-dependent glutathione S-transferase π homologue GST-1 inhibits dopamine neuron degeneration in a Caenorhabditis elegans model of manganism. / Settivari, Raja; VanDuyn, Natalia; LeVora, Jennifer; Nass, Richard.

In: NeuroToxicology, Vol. 38, 09.2013, p. 51-60.

Research output: Contribution to journalArticle

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