UNMC CoNDA Center Seminar with Dr. Jenny Hsieh (University of Texas at San Antonio"
Friday, October 21, 2022 12pm to 1pm
About this Event
“Stem Cell approaches to understand Acquired and Genetic Epilepsies” presented by Dr. Jenny Hsieh, Professor and Department Chair, Neuroscience, Developmental and Regenerative Biology, University of Texas at San Antonio.
Dr. Hsieh's seminar will take place via Zoom from 12:00-1:00pm on Friday, October 21st.
Part of UNMC's Cognitive Neuroscience of Development and Aging Center's Seminar Series.
ABSTRACT: The Hsieh lab focuses on the mechanisms that promote neural stem cell self-renewal and differentiation in embryonic and adult brain. Using mouse models, video-EEG monitoring, viral techniques, and imaging/electrophysiological approaches, we elucidated many of the key transcriptional/epigenetic regulators of adult neurogenesis and showed aberrant new neuron integration in adult rodent hippocampus contribute to circuit disruption and seizure development. Building on this work, I will present our recent studies describing how GABA-mediated Ca2+ activity regulates the production of aberrant adult-born granule cells. In a second direction of my laboratory, we are using human induced pluripotent stem cells and brain organoid models as approaches to understand brain development and disease. Mutations in one gene, Aristaless-related homeobox (ARX), are of considerable interest since they are known to cause a common spectrum of neurodevelopmental disorders including epilepsy, autism, and intellectual disability. We have generated cortical and subpallial organoids from patients with poly-alanine expansion mutations in ARX. To understand the nature of ARX mutations in the organoid system, we are currently performing cellular, molecular, and physiological analyses. I will present these data to gain a comprehensive picture of the effect of ARX mutations in brain development. Since we do not understand how human brain development is affected by ARX mutations that contribute to epilepsy, we believe these studies will allow us to understand the mechanism of pathogenesis of ARX mutations, which has the potential to impact the diagnosis and care of patients.
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Dial-In Information
https://unmc.zoom.us/j/95530202960?pwd=NkJoWUJzc01GVGtzYWluTU9ENG5CUT09
Meeting ID: 955 3020 2960
Passcode: 561772
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