4.7 Review

A deadly spread: cellular mechanisms of α-synuclein transfer

Journal

CELL DEATH AND DIFFERENTIATION
Volume 18, Issue 9, Pages 1425-1433

Publisher

SPRINGERNATURE
DOI: 10.1038/cdd.2011.53

Keywords

Parkinson's disease; alpha-synuclein; prion-like; seeding; aggregation

Funding

  1. MJ Fox Foundation for Parkinson's Research
  2. Swedish Brain Foundation
  3. Swedish Parkinson Foundation
  4. Soderbergs Foundation
  5. Swedish Research Council
  6. Anna-Lisa Rosenberg Foundation
  7. Human Frontier Science Program
  8. ERA-net Neuron program MIPROTRAN

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Classically, Parkinson's disease (PD) is linked to dopamine neuron death in the substantia nigra pars compacta. Intracytoplasmic protein inclusions named Lewy bodies, and corresponding Lewy neurites found in neuronal processes, are also key features of the degenerative process in the substantia nigra. The molecular mechanisms by which substantia nigra dopamine neurons die and whether the Lewy pathology is directly involved in the cell death pathway are open questions. More recently, it has become apparent that Lewy pathology gradually involves greater parts of the PD brain and is widespread in late stages. In this review, we first discuss the role of misfolded alpha-synuclein protein, which is the main constituent of Lewy bodies, in the pathogenesis of PD. We then describe recent evidence that alpha-synuclein might transfer between cells in PD brains. We discuss in detail the possible molecular mechanisms underlying the proposed propagation and the likely consequences for cells that take up a-synuclein. Finally, we focus on aspects of the pathogenic process that could be targeted with new pharmaceutical therapies or used to develop biomarkers for early PD detection. Cell Death and Differentiation (2011) 18, 1425-1433; doi:10.1038/cdd.2011.53; published online 13 May 2011

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