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α-Synuclein and Mitochondrial Dysfunction in Parkinson's Disease

Journal

MOLECULAR NEUROBIOLOGY
Volume 47, Issue 2, Pages 587-597

Publisher

SPRINGER
DOI: 10.1007/s12035-013-8394-x

Keywords

alpha-Synuclein; Parkinson's disease; Lewy bodies

Categories

Funding

  1. Wellcome Trust/MRC Joint Call in Neurodegeneration award [WT089698]
  2. Parkinson's UK
  3. Kattan Trust
  4. Medical Research Council [MC_G1000735] Funding Source: researchfish
  5. MRC [MC_G1000735] Funding Source: UKRI

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alpha-Synuclein (SNCA) is a substantive component of Lewy bodies, the pathological hallmark of Parkinson's disease (PD). The discovery and subsequent derivation of its role in PD has led to a suprising but fruitful convergence of the fields of biochemistry and molecular genetics. In particular, the manipulation of the cell lines of a number of forms of familial PD has implicated SNCA in distinct and diverse biochemical pathways related to its pathogenesis. This current and rapidly evolving concept indicates PD is a disease in which interacting pathways of oxidative stress, mitochondrial dysfunction and impaired regulation of protein turnover interact to cause dopaminergic cell dysfunction and death. SNCA has a central role in these processes and manipulation of its expression, degradation and aggregation appear to be promising neuroprotective therapeutic targets.

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