Hydrodynamic delivery for the study, treatment and prevention of acute kidney injury

dc.contributor.advisorAtkinson, Simon
dc.contributor.authorCorridon, Peter R.
dc.contributor.otherBasile, David P.
dc.contributor.otherBacallao, Robert L.
dc.contributor.otherDunn, Kenneth William
dc.contributor.otherGattone II, Vincent H.
dc.date.accessioned2014-07-07T18:00:37Z
dc.date.available2014-07-07T18:00:37Z
dc.date.issued2014-07-07
dc.degree.date2013en_US
dc.degree.disciplineBiomolecular Imaging & Biophysicsen
dc.degree.grantorIndiana Universityen_US
dc.degree.levelPh.D.en_US
dc.descriptionIndiana University-Purdue University Indianapolis (IUPUI)en_US
dc.description.abstractAdvancements in human genomics have simultaneously enhanced our basic understanding of the human body and ability to combat debilitating diseases. Historically, research has shown that there have been many hindrances to realizing this medicinal revolution. One hindrance, with particular regard to the kidney, has been our inability to effectively and routinely delivery genes to various loci, without inducing significant injury. However, we have recently developed a method using hydrodynamic fluid delivery that has shown substantial promise in addressing aforesaid issues. We optimized our approach and designed a method that utilizes retrograde renal vein injections to facilitate widespread and persistent plasmid and adenoviral based transgene expression in rat kidneys. Exogenous gene expression extended throughout the cortex and medulla, lasting over 1 month within comparable expression profiles, in various renal cell types without considerably impacting normal organ function. As a proof of its utility we by attempted to prevent ischemic acute kidney injury (AKI), which is a leading cause of morbidity and mortality across among global populations, by altering the mitochondrial proteome. Specifically, our hydrodynamic delivery process facilitated an upregulated expression of mitochondrial enzymes that have been suggested to provide mediation from renal ischemic injury. Remarkably, this protein upregulation significantly enhanced mitochondrial membrane potential activity, comparable to that observed from ischemic preconditioning, and provided protection against moderate ischemia-reperfusion injury, based on serum creatinine and histology analyses. Strikingly, we also determined that hydrodynamic delivery of isotonic fluid alone, given as long as 24 hours after AKI is induced, is similarly capable of blunting the extent of injury. Altogether, these results indicate the development of novel and exciting platform for the future study and management of renal injury.en_US
dc.identifier.urihttps://hdl.handle.net/1805/4603
dc.identifier.urihttp://dx.doi.org/10.7912/C2/2128
dc.language.isoen_USen_US
dc.subjectAcute kidney injuryen_US
dc.subjectConfocal microscopyen_US
dc.subjectGene deliveryen_US
dc.subjectHydrodynamic deliveryen_US
dc.subjectIntravital two photon fluorescent microscopyen_US
dc.subjectRenal gene therapyen_US
dc.subject.lcshKidneys -- Wounds and injuries -- Research -- Evaluationen_US
dc.subject.lcshAcute renal failureen_US
dc.subject.lcshConfocal fluorescence microscopy -- Research -- Evaluation -- Analysisen_US
dc.subject.lcshFluorescence microscopy -- Researchen_US
dc.subject.lcshThree-dimensional imaging in medicine -- Research -- Evaluation -- Analysisen_US
dc.subject.lcshKidneys -- Diseases -- Gene therapyen_US
dc.subject.lcshKidneys -- Diseases -- Diagnosisen_US
dc.subject.lcshKidneys -- Pathophysiologyen_US
dc.subject.lcshGene therapy -- Researchen_US
dc.subject.lcshImage processingen_US
dc.subject.lcshMitochondrial membranes -- Researchen_US
dc.subject.lcshHistology -- Techniqueen_US
dc.subject.lcshPhysiologic salinesen_US
dc.subject.lcshBiophysics -- Research -- Evaluationen_US
dc.subject.lcshGene targetingen_US
dc.subject.lcshMultiphoton excitation microscopyen_US
dc.subject.lcshKidneys -- Imagingen_US
dc.subject.lcshTransgenes -- Expressionen_US
dc.titleHydrodynamic delivery for the study, treatment and prevention of acute kidney injuryen_US
dc.typeThesisen
Files
Original bundle
Now showing 1 - 1 of 1
No Thumbnail Available
Name:
P Corridon Final Full Thesis (Final Submitted Nov 1).pdf
Size:
14.09 MB
Format:
Adobe Portable Document Format
License bundle
Now showing 1 - 1 of 1
No Thumbnail Available
Name:
license.txt
Size:
1.88 KB
Format:
Item-specific license agreed upon to submission
Description: