Scientists unravel molecular mechanisms of Parkinson's disease

June 12, 2018 in Medicine & Health / Parkinson's & Movement disorders
Scientists unravel molecular mechanisms of Parkinson’s disease
Credit: The Francis Crick Institute

Detailed brain cell analysis has helped researchers uncover new mechanisms thought to underlie Parkinson's disease.

The study, published in Nature Communications, adds to our growing understanding of the causes of Parkinson's and other neurodegenerative diseases, and could influence drug design in the future.

For years, scientists have known that Parkinson's disease is associated with a build-up of protein inside . But how these protein clumps cause neurons to die was a mystery.

Using a combination of detailed cellular and molecular approaches to compare healthy and clumped forms of alpha-synuclein, a team of scientists at the Francis Crick Institute, UCL, UK Dementia Research Institute at the universities of Cambridge and Edinburgh, New York University and other collaborators have discovered how the protein clumps are toxic to neurons.

They found that clumps of alpha-synuclein moved to and damaged key proteins on the surface of mitochondria - the energy powerhouses of cells - making them less efficient at producing energy. It also triggered a channel on the surface of mitochondria to open, causing them to swell and burst, leaking out chemicals that tell the cell to die.

Scientists unravel molecular mechanisms of Parkinson’s disease
Super-resolution image of α-synuclein in mitochondria of neuron (left) and single molecule TIRF image of individual α-synuclein aggregates (right). Credit: Mathew Horrocks

These findings were replicated in human cells, generated from of patients with a mutation in the alpha-synuclein gene, which causes early-onset Parkinson's disease. By turning patient skin cells into , they could chemically guide them into become brain that could be studied in the lab. This cutting-edge technique provides a valuable insight into the earliest stages of neurodegeneration - something that brain scans and post-mortem analysis cannot capture.

Sonia Gandhi, Group Leader at the Crick and UCL, and joint senior author of the study said: "Our findings give us huge insight into why protein clumping is so damaging in Parkinson's, and highlight the need to develop therapies against the toxic form of alpha-synuclein, not the healthy non-clumped form."

Andrey Abramov, joint senior author of the paper said: "This study was a complex collaboration at the interface of chemistry, biophysics and biology, bringing scientists from different disciplines together to investigate a longstanding problem in Parkinson's research."

More information: Marthe H. R. Ludtmann et al. α-synuclein oligomers interact with ATP synthase and open the permeability transition pore in Parkinson's disease, Nature Communications (2018). DOI: 10.1038/s41467-018-04422-2

Provided by The Francis Crick Institute

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