Title:
Engineering Tools to Promote and Characterize Wnt-Mediated Stem Cell Differentiation

dc.contributor.advisor Kane, Ravi S.
dc.contributor.author Stathos, Mark
dc.contributor.committeeMember Garcia, Andres
dc.contributor.committeeMember Platt, Manu
dc.contributor.committeeMember Sulchek, Todd
dc.contributor.committeeMember Wu, Ronghu
dc.contributor.department Mechanical Engineering
dc.date.accessioned 2022-08-25T13:30:20Z
dc.date.available 2022-08-25T13:30:20Z
dc.date.created 2021-08
dc.date.issued 2021-08-02
dc.date.submitted August 2021
dc.date.updated 2022-08-25T13:30:21Z
dc.description.abstract The Wnt signaling pathway plays an important role in the development of many tissues in the body from the earliest stage of the process. However, the mechanisms of the Wnt pathway and the roles it plays in development remain incompletely understood. This is in part due to the complexity of embryonic development and in part due to the hydrophobicity of Wnt ligands. To overcome issues associated with the use of natural Wnt ligands, we have developed a heterodimer of Fabs which bind to the Wnt co-receptors LRP6 and Frizzled. We have shown that this dimer can activate Wnt signaling with an efficacy comparable to that of the natural ligand. To elucidate the mechanisms of downstream events in the Wnt pathway, we constructed a kinetic model consisting of a system of ordinary differential equations. We fit this model to empirical time course data derived from Western blots of HEK293T cells treated with Wnt. From this fit we were able to gain insights into how the intracellular levels of the Wnt pathway component β-catenin are regulated. To better characterize the downstream effects of Wnt signaling during the manufacturing of therapeutic cells, we also generated CRISPR/Cas9 edited reporter iPSC lines which are designed to detect the expression of Wnt-regulated marker genes with high specificity. Luminescent signals produced with the help of luciferase secreted by these cell lines during directed differentiation into cardiomyocytes permit continuous non-destructive monitoring of the manufacturing process. These cell lines could potentially guide process optimization and enable production of cardiomyocytes with a more mature phenotype.
dc.description.degree Ph.D.
dc.format.mimetype application/pdf
dc.identifier.uri http://hdl.handle.net/1853/67163
dc.language.iso en_US
dc.publisher Georgia Institute of Technology
dc.subject Protein engineering
dc.subject Cell signaling
dc.subject Wnt
dc.subject Stem cell differentiation
dc.subject Cardiomyocytes
dc.subject Genome editing
dc.subject CRISPR
dc.subject Kinetic modeling
dc.title Engineering Tools to Promote and Characterize Wnt-Mediated Stem Cell Differentiation
dc.type Text
dc.type.genre Dissertation
dspace.entity.type Publication
local.contributor.advisor Kane, Ravi S.
local.contributor.corporatename George W. Woodruff School of Mechanical Engineering
local.contributor.corporatename College of Engineering
relation.isAdvisorOfPublication 35bafb8e-f759-4618-9d00-c736c2303f60
relation.isOrgUnitOfPublication c01ff908-c25f-439b-bf10-a074ed886bb7
relation.isOrgUnitOfPublication 7c022d60-21d5-497c-b552-95e489a06569
thesis.degree.level Doctoral
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