| Literature DB >> 24899725 |
Mohammad Parsanejad1, Yi Zhang1, Dianbo Qu1, Isabella Irrcher2, Maxime W C Rousseaux1, Hossein Aleyasin1, Fatemeh Kamkar1, Steve Callaghan1, Ruth S Slack1, Tak W Mak3, Stephen Lee1, Daniel Figeys4, David S Park5.
Abstract
DJ-1 (PARK7) is a gene linked to autosomal recessive Parkinson disease (PD). We showed previously that DJ-1 loss sensitizes neurons in models of PD and stroke. However, the biochemical mechanisms underlying this protective role are not completely clear. Here, we identify Von Hippel Lindau (VHL) protein as a critical DJ-1-interacting protein. We provide evidence that DJ-1 negatively regulates VHL ubiquitination activity of the α-subunit of hypoxia-inducible factor-1 (HIF-1α) by inhibiting HIF-VHL interaction. Consistent with this observation, DJ-1 deficiency leads to lowered HIF-1α levels in models of both hypoxia and oxidative stress, two stresses known to stabilize HIF-1α. We also demonstrate that HIF-1α accumulation rescues DJ-1-deficient neurons against 1-methyl-4-phenylpyridinium-induced toxicity. Interestingly, lymphoblast cells extracted from DJ-1-related PD patients show impaired HIF-1α stabilization when compared with normal individuals, indicating that the DJ-1-VHL link may also be relevant to a human context. Together, our findings delineate a model by which DJ-1 mediates neuronal survival by regulation of the VHL-HIF-1α pathway.Entities:
Keywords: DJ-1; Parkinson's disease; oxidative stress
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Year: 2014 PMID: 24899725 PMCID: PMC6608259 DOI: 10.1523/JNEUROSCI.1244-13.2014
Source DB: PubMed Journal: J Neurosci ISSN: 0270-6474 Impact factor: 6.167