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Scientists Discover Key Cellular Mechanism Underlying Parkinson’s Disease

 

Scientists Discover Key Cellular Mechanism Underlying Parkinson’s Disease

By Will Doss

Northwestern Medicine scientists have identified a toxic cascade that leads to neuronal degeneration in patients with Parkinson’s disease (PD), findings published in the journal Science.

Led by Dimitri Krainc, MD, PhD, the Aaron Montgomery Ward Professor and chair of The Ken and Ruth Davee Department of Neurology, the study showed how interventions early in the disease process may be able to break the pathogenic cycle and improve neuronal function in PD. The scientists also examined how mouse models of PD compared to abnormalities they found in human PD neurons, shedding new light on the importance of studies in human neurons for the development of new therapies.

Krainc was senior author on the study and Lena Burbulla, PhD, a postdoctoral fellow in Krainc’s laboratory, was the first author.

Dimitri Krainc, MD, PhD, the Aaron Montgomery Ward Professor and chair of The Ken and Ruth Davee Department of Neurology, was lead author on a study that discovered a toxic cascade that underlies the development of Parkinson’s Disease.

 

PD is the second-most common neuro-degenerative disorder, primarily caused by the death of dopamine-containing neurons in the substantia nigra, a region of the brain involved in motor control. While people naturally lose dopamine neurons as they age, patients with PD lose a much larger number of these neurons and the remaining cells are no longer able to compensate, leading to disease, according to previous research.

Understanding how and why these neurons die is an important step in identifying treatments, Krainc said. While previous research indicated that the cellular mechanism behind the cell death involved the mitochondria and lysosomes, how these two pathways converge in dopamine neurons to cause cell death remained unknown up until now.

Using human neurons from Parkinson’s patients, Krainc and colleagues identified a toxic cascade of mitochondrial and lysosomal dysfunction initiated by an accumulation of oxidized dopamine and a protein called alpha-synuclein. Specifically, the current study demonstrated that an accumulation of oxidized dopamine depressed the activity of lysosomal glucocerebrosidase (GCase), an enzyme previously implicated in PD. That depression in turn weakened overall lysosomal function and contributed to the degeneration of neurons.

The accretion of oxidized dopamine didn’t just interfere with lysosomes, however. Krainc and his colleagues discovered that the dopamine also damaged the neurons’ mitochondria by increasing mitochondrial oxidant stress. These dysfunctional mitochondria led to increased oxidized dopamine levels, creating a vicious cycle.

“The mitochondrial and lysosomal pathways are two critical pathways in disease development,” said Krainc, also the director of the Center for Rare Neurological Diseases and a professor of Neurological Surgery and Physiology. “Combined with the alpha-synuclein accumulation, this study links the major pathological features of PD.”

Once they had catalogued this toxic cascade, Krainc and his colleagues began looking for ways to interrupt it, he said.

“One of the key strategies that worked in our experiments is to treat dopamine neurons early in the toxic cascade with specific antioxidants that improve mitochondrial oxidant stress and lower oxidized dopamine,” Krainc said. “With this approach, we found that we can attenuate or prevent the downstream toxic effects in human dopaminergic neurons.”

This approach to interrupting the toxic cascade of oxidized dopamine may provide a target for the development of future therapies. However, identifying patients with early stage neurodegeneration can be difficult, because damage has often occurred far before any symptoms are apparent, according to Krainc.

Consequently, genetic testing will be central to future diagnostic efforts. Causative genes are prime candidates for screening, while risk genes such as GBA1 are less conclusive but still important markers, according to Krainc.

Early detection will also rely on brain imaging and other clinical signifiers, Krainc said.

“For example, in Parkinson’s it’s well-known many sufferers have a specific type of sleep disorder,” he said. “That starts 10 to 15 years before other symptoms, so it can serve as a predictor of Parkinson’s disease.”

Interestingly, when compared to human cellular models, mouse models of PD did not demonstrate the same toxic cascade, according to the study. Krainc and his colleagues theorized this is due to differences in metabolism of dopamine between species, and underscored the importance of studying human neurons to discover new targets for drug development.

This work was supported by National Institutes of Health (NIH) grants R01NS076054, NS047085, R01NS092823, R00DC013805-02, T32NS041234 and F32NS101778; JPB Foundation, Michael J. Fox Foundation for Parkinson’s Research and IDP Foundation; German Academic Exchange Service; Les Turner ALS Foundation, Target ALS and MDA; German Research Council, KR2119/8-1; and the Fond National de programme, FNR/P13/6682797.

source: Northwestern University

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