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There is now a CONTENT FREEZE for Mercury while we switch to a new platform. It began on Friday, March 10 at 6pm and will end on Wednesday, March 15 at noon. No new content can be created during this time, but all material in the system as of the beginning of the freeze will be migrated to the new platform, including users and groups. Functionally the new site is identical to the old one. webteam@gatech.edu
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Advisor:
Robert Gross, MD, PhD (Emory University)
Committee:
Michelle LaPlaca, PhD (Georgia Institute of Technology)
Mark Prausnitz, PhD (Georgia Institute of Technology)
Ravi Kane, PhD (Georgia Institute of Technology)
Jae-Kyung (Jamise) Lee, PhD (University of Georgia)
Development and Characterization of Viral Vectors for Stress-Dependent Transgene Expression in Neurons
The overarching goal of this work was to design and characterize expression vectors that were responsive to physiological changes associated with neurodegenerative disease. The development of this molecular tool responds to the need for physiologically responsive constructs designed to prevent unwanted side effects related to transgene overexpression in current gene therapy interventions. To accomplish this, we adopted regulatory elements from the unfolded protein response (UPR), a homeostatic mechanism used by cells to cope with stress. Thus, by harnessing a biological signal associated with how cells respond to stress conditions, we created stress-responsive viral vectors and demonstrated their use in neurons. This thesis describes the characterization of these vectors by extensive time-lapse fluorescent microscopy assays in several in vitro models of proteostasis dysfunction, including er stress, proteasome inactivation, phosphatase inhibition, and alpha-synuclein overexpression. Collectively, our results demonstrate the feasibility of mobilizing cellular stress signaling to create physiologically-responsive viral vectors for use in neuroscience.
