Dr. Scott Ryan

The Ryan Lab strives to answer fundamental questions in neuroscience, develop new tools for collaborative investigation into the mechanisms underlying neurological disorders and train scientists in the areas of molecular neuroscience and stem cell biology.

Theme 1: Stem Cell Modelling of Neurodegenerative Disease

When studying the mechanisms of neurodegenerative disease, the traditional animal systems, while powerful, have limitations to what they can teach. These systems utilize genetic over-expression or silencing paradigms to understand basic processes. While animal models have lead to huge advancements in our understanding of neurobiology, there is controversy over whether overexpression/silencing of gene expression is representative of diverse disease states. Indeed, the lack of availability of primary human neurons has made evaluating the pathological consequences of genomic mutations arduous. The use of human induced pluripotent stem cell (hiPSC) technology overcomes these limitations by providing a source of human neurons from both normal and disease genetic backgrounds. We currently focus on stem cell based models of Parkinson's Disease (PD) to study how mitochondrial stress mechanisms impact on neuronal function in human disease.

Theme 2: Building Blocks Of Memory

Learning and memory has at its core modifications to tiny spine like structures that exist on a special subset of neurons in the brain known as “spiny neurons.” These spines must move, adapt, grow and retract in response to chemical neurotransmitters in the brain, a process that as a whole is believed to be the cellular manifestation of learning, known as synaptic plasticity. The spines themselves are thought to serve as basic units of memory storage. While much work has focused directly on the chemical signals that mediate communication in the brain and the ion channels that are opened as a result, little is known of the specific signalling pathways that control the actual generation, shape and loss of individual spines. Nitric Oxide is unique second messenger in that it can directly alter the proteins responsible for dynamic changes to spine morphology. Nitric Oxide signalling may regulate synaptic plasticity by altering the density and morphology of spines through a process called S-nitrosylation. We are monitoring what proteins are S-nitrosylated by Nitric Oxide under conditions of spine growth, spine stabilization and spine retraction. This research will further our understanding neural architecture and the means by which cells of the brain communicate. 

Theme 3: Repopulating the Brain

Stem cells are found throughout the body during both development and adulthood. They have the unique capacity to continuously divide and to produce daughter cells with a multitude of identities. In the nervous system, this process give rise to neural precursor cells that populate the developing brain with both neurons and glia, while renewing their own population at the same time. We are attempting to overcome the limited repair observed in many neurological disorders by employing directed differentiation to replenish lost or damaged tissue in the brain.

• 2003 - B.Sc. Honours (Biochemistry/Nutrition) - Memorial University of Newfoundland
• 2008 - Ph.D. (Biochemistry), University of Ottawa
• 2009-2011 - Postdoctoral Fellow, Ottawa Hospital Research Institute
• 2011-2013 - Postdoctoral Fellow, Sanford Burnham Medical Research Institute

• Ryan SD, Dolatabadi N, Chan SF, Zhang X, Akhtar MW, Parker J, Soldner F, Sunico CR, Nagar S, Talantova M, Lee B, Lopez K, Nutter A, Shan B, Molokanova E, Zhang Y, Han X, Masliah E, Yates JR, Nakanishi N, Andreyev A, Okamoto S, Jaenisch R, Ambasudhan R, Lipton SA (2013) Isogenic Human iPSC Parkinson’s Model Shows Nitrosative Stress-Induced Dysfunction in MEF2-PGC1α Transcription. Cell, Dec 5:155(6) 1351. *Profiled by Amanda Woerner, FOX News (Nov 27, 2013)
• Nakanichi N, Ryan SD, Holland T, Cho EG, Liao F-F, Xu X, Lipton SA, Tu S (2012) Synaptic protein α1-takusan mitigates Aβ-induced synaptic loss via its interaction with PSD-95 and tau at postsynaptic sites.  J. Neurosci,Aug 28;33(35):14170-83
• Piña-Crespo JC, Talantova M, Cho EG, Soussou W, Dolatabadi N, Ryan SDAmbasudhan R, McKercher S, Deisseroth K, Lipton SA (2012) High-frequency hippocampal oscillations activated by optogenetic stimulation of transplanted human ESC-derived neurons.J. Neurosci Nov 7;32(45):15837-42 *Profiled in ScienceDaily, (Nov. 15, 2012)
• Ryan SD, Bhanot K, Ferrier A, De Repentingy Y, Chu A, Blais A, Kothary R (2012) Microtubule stability, Golgi organization, and transport flux require dystonin-a2/MAP1B interaction. J. Cell Biol. Mar;196(6) *Profiled in NewsRx (April 20th 2012)
• Ryan SD, Ferrier A, Sato T, O’Meara RW, De Repentingy Y, Jiang SX, Hou ST, Kothary R (2011) Neuronal dystonin isoform 2 is a novel mediator of endoplasmic reticulum structure and function. Mol Biol Cell, Feb;23(4):553-66
• O’Meara RW, Ryan SD, Colognato H, Kothary R (2011) Derivation of enriched oligodendrocyte cultures and oligodendrocyte/neuron myelinating co-cultures from post-natal murine tissues. Journal of Visual Experimentation (JOVE) Aug 21;(54). pii: 3324. doi: 10.3791/3324
• Ryan SD, Whitehead, SN, Swayne L, Moffat, TC, Hou W, Ethier M, Bourgeois AJG, Rashidian J, Fraser PE, Figeys D, Park DS, Bennett SAL  (2009) Disruption of alkylacylglycerophosphocholines by amyloid-b42 signals tau hyperphosphorylation and compromises neuronal viability.  PNAS, Dec 8;106(49):20936-41 *Profiled in Alzheimer Research Forum (Nov 22, 2009) *Profiled in CrossBorder Biotech. (Nov 27 2009)