Article
The morphological basis of mental dysfunction in Parkinson's disease.
Institute of Clinical Neurobiology, Kenyongasse 18, A-1070 Vienna, Austria.
Journal of the Neurological Sciences (impact factor:
2.35).
11/2006;
248(1-2):167-72.
DOI:10.1016/j.jns.2006.05.002
pp.167-72
Source: PubMed
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Citations (0)
- Cited In (1)
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Article: DJ-1 modulates alpha-synuclein aggregation state in a cellular model of oxidative stress: relevance for Parkinson's disease and involvement of HSP70.
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ABSTRACT: Parkinson's disease (PD) is a neurodegenerative pathology whose molecular etiopathogenesis is not known. Novel contributions have come from familial forms of PD caused by alterations in genes with apparently unrelated physiological functions. The gene coding for alpha-synuclein (alpha-syn) (PARK1) has been investigated as alpha-syn is located in Lewy bodies (LB), intraneuronal inclusions in the substantia nigra (SN) of PD patients. A-syn has neuroprotective chaperone-like and antioxidant functions and is involved in dopamine storage and release. DJ-1 (PARK7), another family-PD-linked gene causing an autosomal recessive form of the pathology, shows antioxidant and chaperone-like activities too. The present study addressed the question whether alpha-syn and DJ-1 interact functionally, with a view to finding some mechanism linking DJ-1 inactivation and alpha-syn aggregation and toxicity. We developed an in vitro model of alpha-syn toxicity in the human neuroblastoma cell line SK-N-BE, influencing DJ-1 and alpha-syn intracellular concentrations by exogenous addition of the fusion proteins TAT-alpha-syn and TAT-DJ-1; DJ-1 was inactivated by the siRNA method. On a micromolar scale TAT-alpha-syn aggregated and triggered neurotoxicity, while on the nanomolar scale it was neuroprotective against oxidative stress (induced by H(2)O(2) or 6-hydroxydopamine). TAT-DJ-1 increased the expression of HSP70, while DJ-1 silencing made SK-N-BE cells more susceptible to oxidative challenge, rendering TAT-alpha-syn neurotoxic at nanomolar scale, with the appearance of TAT-alpha-syn aggregates. DJ-1 inactivation may thus promote alpha-syn aggregation and the related toxicity, and in this model HSP70 is involved in the antioxidant response and in the regulation of alpha-syn fibril formation.PLoS ONE 02/2008; 3(4):e1884. · 4.09 Impact Factor
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Keywords
additional pathologies
cognitive dysfunction
cognitive impairment
consecutive autopsy series
demented PD cases
essential morphological changes
limbic Lewy bodies
limbic Lewy body
Mental dysfunction
negative relation
neuritic AD lesions
neuritic AD pathology
neuritic Alzheimer pathologies
Parkinson's disease
PD patients
severe neuritic AD lesions
shorter survival
six-fold lifetime risk
synergistic reaction
tau-pathologies