AI Article Synopsis

  • - Research on Parkinson's disease is limited due to the difficulty in accessing diseased tissue; induced pluripotent stem cells (iPSCs) derived from patients offer a potential solution.
  • - A specific genetic mutation, the triplication of the SNCA gene, is linked to a severe form of Parkinson's disease characterized by increased production of the α-synuclein protein, which plays a key role in the disease's development.
  • - Scientists created iPSC lines from both a patient with SNCA triplication and a healthy relative, finding that the patient's neurons produce twice the normal levels of α-synuclein, providing a new model to investigate treatments and the underlying mechanisms of neurodegeneration.

Article Abstract

A major barrier to research on Parkinson's disease is inaccessibility of diseased tissue for study. One solution is to derive induced pluripotent stem cells from patients and differentiate them into neurons affected by disease. Triplication of SNCA, encoding α-synuclein, causes a fully penetrant, aggressive form of Parkinson's disease with dementia. α-Synuclein dysfunction is the critical pathogenic event in Parkinson's disease, multiple system atrophy and dementia with Lewy bodies. Here we produce multiple induced pluripotent stem cell lines from an SNCA triplication patient and an unaffected first-degree relative. When these cells are differentiated into midbrain dopaminergic neurons, those from the patient produce double the amount of α-synuclein protein as neurons from the unaffected relative, precisely recapitulating the cause of Parkinson's disease in these individuals. This model represents a new experimental system to identify compounds that reduce levels of α-synuclein, and to investigate the mechanistic basis of neurodegeneration caused by α-synuclein dysfunction.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3265381PMC
http://dx.doi.org/10.1038/ncomms1453DOI Listing

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