Simonetta Sipione

Biography

Simonetta Sipione is a professor belongs to the department of Pharmacology from the university of Alberta.

Research Interest

We use a multidisciplinary approach to study Huntington's disease (HD), one of the most common inherited neurodegenerative disorders. HD is due to the expansion of a polyglutamine stretch in a protein named huntingtin. Similar to Alzheimer and Parkinson, HD causes specific neurons to die, leading to motor and cognitive dysfunction. The exact mechanism by which neurodegeneration occurs in HD is poorly understood. Before dying, HD neurons displays a wide array of cell dysfunctions, including aberrant cell signaling and neurotransmission, dysregulation of gene expression and impaired mitochondrial metabolism. Our goal is to elucidate the cellular and molecular mechanisms responsible for neuronal dysfunction and death in HD, and to identify potential treatments for this devastating disease. Main research projects: 1. Lipids and HD. HD neurons have impaired synthesis of cholesterol and gangliosides, lipid molecules that are highly enriched in the brain. Both cholesterol and gangliosides are important components of membrane micro-domains that serve as hubs for cell signaling, and are crucial for many brain functions. Therefore, decreased synthesis of these lipids is likely to have profound effects on HD pathogenesis. We study the role of cholesterol and gangliosides in cell signaling defects and in cell death in HD, as well as their effects on motor and cognitive behavior in transgenic HD mouse models, and their potential therapeutic use. 2. Mutant huntingtin and the transcription of cholesterogenic genes. We study the transcription factors that regulate the expression of lipid-related genes, and how they work in normal and HD cells. 3. Post-translational modifications of mutant huntingtin toxicity. Recent studies suggest that the intracellular localization, function and toxicity of mutant huntingtin can be regulated by post-translational protein modifications such as phosphorylation, ubiquitination and others. We are interested in understanding how neuroprotective post-translational modifications of huntingtin are triggered, in order to identify novel therapeutic targets.