Cytoplasmic Pink1 activity protects neurons from dopaminergic neurotoxin MPTP

M. Emdadul Haque, Kelly J. Thomas, Cheryl D'Souza, Steve Callaghan, Tohru Kitada, Ruth S. Slack, Paul Fraser, Mark R. Cookson, Anurag Tandon, David S. Park

Research output: Contribution to journalArticlepeer-review

211 Citations (Scopus)

Abstract

PTEN-induced putative kinase 1 (Pink1) is a recently identified gene linked to a recessive form of familial Parkinson's disease (PD). The kinase contains a mitochondrial localization sequence and is reported to reside, at least in part, in mitochondria. However, neither the manner by which the loss of Pink1 contributes to dopamine neuron loss nor its impact on mitochondrial function and relevance to death is clear. Here, we report that depletion of Pink1 by RNAi increased neuronal toxicity induced by MPP+. Moreover, wild-type Pink1, but not the G309D mutant linked to familial PD or an engineered kinase-dead mutant K219M, protects neurons against MPTP both in vitro and in vivo. Intriguingly, a mutant that contains a deletion of the putative mitochondrial-targeting motif was targeted to the cytoplasm but still provided protection against 1-methyl-4-phenylpyridine (MPP+)/1-methyl-4- phenyl-1,2,3,6-tetrahydropyridine (MPTP)-induced toxicity. In addition, we also show that endogenous Pink1 is localized to cytosolic as well as mitochondrial fractions. Thus, our findings indicate that Pink1 plays a functional role in the survival of neurons and that cytoplasmic targets, in addition to its other actions in the mitochondria, may be important for this protective effect.

Original languageEnglish
Pages (from-to)1716-1721
Number of pages6
JournalProceedings of the National Academy of Sciences of the United States of America
Volume105
Issue number5
DOIs
Publication statusPublished - Feb 5 2008
Externally publishedYes

Keywords

  • Neurodegeneration
  • Neuroprotection
  • Parkinson's disease

ASJC Scopus subject areas

  • General

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