Show simple item record

Modeling Tuberous Sclerosis Complex Using Patient-Derived Cells

dc.creatorArmstrong, Laura Craig
dc.date.accessioned2020-08-22T21:03:14Z
dc.date.available2018-09-21
dc.date.issued2017-09-21
dc.identifier.urihttps://etd.library.vanderbilt.edu/etd-09162017-134651
dc.identifier.urihttp://hdl.handle.net/1803/14161
dc.description.abstractTuberous Sclerosis Complex (TSC) is a pediatric disorder of dysregulated growth and differentiation caused by loss of function mutations in either the TSC1 or TSC2 genes, which regulate mTOR kinase activity. TSC causes refractory epilepsy and intellectual disability but the pathogenesis of the neurological symptoms is not understood. Identifying when and in what cell types mutations in TSC1 or TSC2 lead to neurological dysfunction is the first step to better and more targeted treatments. To study aberrations of early development in TSC, we generated induced pluripotent stem cells using dermal fibroblasts obtained from patients with TSC. During validation, we found that stem cells generated from TSC patients had a very high rate of integration of the reprograming plasmid containing a shRNA against TP53. Loss of one allele of TSC2 in human fibroblasts is sufficient to increase p53 levels and impair stem cell reprogramming. Increased p53 was also observed in TSC2 heterozygous and homozygous mutant human stem cells, suggesting that the interactions between TSC2 and p53 are consistent across cell types and gene dosage. Further, we show that homozygous loss of TSC2 leads to increased mTORC1 in neural progenitors and impaired neural progenitor formation. These results support the contributions of TSC2 heterozygous and homozygous mutant cells to the pathogenesis of TSC and the important role of p53 during reprogramming.
dc.format.mimetypeapplication/pdf
dc.subjectp53
dc.subjectinduced pluripotent stem cells
dc.subjecttuberous sclerosis complex
dc.subjectmTOR
dc.titleModeling Tuberous Sclerosis Complex Using Patient-Derived Cells
dc.typedissertation
dc.contributor.committeeMemberAaron Bowman
dc.contributor.committeeMemberCharles Hong
dc.contributor.committeeMemberAndrea Page McCaw
dc.contributor.committeeMemberDavid Miller
dc.type.materialtext
thesis.degree.namePHD
thesis.degree.leveldissertation
thesis.degree.disciplineCell and Developmental Biology
thesis.degree.grantorVanderbilt University
local.embargo.terms2018-09-21
local.embargo.lift2018-09-21
dc.contributor.committeeChairKevin Ess


Files in this item

Icon

This item appears in the following Collection(s)

Show simple item record