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An Investigation of the GAPDH/Siah1 Pathway in Human Retinal Pericyte Apoptosis

dc.creatorSuarez, Sandra
dc.date.accessioned2020-08-23T16:13:36Z
dc.date.available2017-12-10
dc.date.issued2015-12-10
dc.identifier.urihttps://etd.library.vanderbilt.edu/etd-12052015-165628
dc.identifier.urihttp://hdl.handle.net/1803/15158
dc.description.abstractDiabetic Retinopathy (DR) is a leading cause of blindness worldwide, and its prevalence is growing. Current therapies for DR address only the later stages of the disease, are invasive and are of limited effectiveness. Retinal pericyte death is an early pathologic
feature of DR. Though it has been observed in diabetic patients and in animal models of DR, the cause of pericyte death remains unknown. A novel pro-apoptotic pathway initiated by the interaction between glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and the E3 ubiquitin ligase, seven in absentia homolog 1 (Siah1), was identified to play a significant role in human retinal pericyte apoptosis. Inhibition of the GAPDH/Siah1 pro-apoptotic complex blocks diabetes-induced pericyte apoptosis, widely considered a hallmark feature of DR.
dc.format.mimetypeapplication/pdf
dc.subjectDiabetic retinopathy
dc.subjectcell death
dc.subjectapoptosis
dc.subjecthigh glucose
dc.subjectGAPDH
dc.subjectSiah1
dc.subjectcell signaling
dc.titleAn Investigation of the GAPDH/Siah1 Pathway in Human Retinal Pericyte Apoptosis
dc.typedissertation
dc.contributor.committeeMemberJohn S. Penn
dc.contributor.committeeMemberDouglas G. McMahon
dc.contributor.committeeMemberDavid M. Miller
dc.contributor.committeeMemberSandra S. Zinkel
dc.type.materialtext
thesis.degree.namePHD
thesis.degree.leveldissertation
thesis.degree.disciplineCell and Developmental Biology
thesis.degree.grantorVanderbilt University
local.embargo.terms2017-12-10
local.embargo.lift2017-12-10
dc.contributor.committeeChairJohn J. Reese


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