Characterization of autologous cell sources for alternatives to aortic valvular interstitial cells in tissue engineered heart valves

dc.contributor.authorAmbrose, Emma
dc.contributor.examiningcommitteeWigle, Jeff (Biochemistry and Medical Genetics)en_US
dc.contributor.supervisorDixon, Ian (Physiology and Pathophysiology) Cattini, Peter (Physiology and Pathophysiology) Halayko, Andrew (Physiology and Pathophysiology)en_US
dc.date.accessioned2016-09-19T15:56:11Z
dc.date.available2016-09-19T15:56:11Z
dc.date.issued2016
dc.degree.disciplinePhysiology and Pathophysiologyen_US
dc.degree.levelMaster of Science (M.Sc.)en_US
dc.description.abstractThe gold standard treatment for patients with AVD is surgical replacement of the aortic valve with either mechanical or fixed tissue prostheses. These implants have a limited lifespan and are associated with serious adverse events. Patient autologous tissue engineered heart valves (TEHVs) offer a solution. Vital to the development of a TEHV is determining a source of donor tissue(s) that most closely mimics the native valve tissue. In pursuit of determining an alternative cell source for patient autologous TEHVs we compared a number of phenotypic and genotypic characteristics of atrial fibroblasts, dermal fibroblasts and differentiated bone marrow-derived progenitor cells (BMCs) and made a comparison to valvular interstitial cells (VICS). We demonstrate that while VICs share some phenotypic similarities with fibroblasts and BMCs, they also possess unique characteristics and demonstrate differential mRNA expression of key regulatory pathways that may influence their phenotype.en_US
dc.description.noteOctober 2016en_US
dc.identifier.urihttp://hdl.handle.net/1993/31804
dc.language.isoengen_US
dc.rightsopen accessen_US
dc.subjectTissue engineered heart valvesen_US
dc.subjectAortic valve diseaseen_US
dc.subjectAortic valveen_US
dc.titleCharacterization of autologous cell sources for alternatives to aortic valvular interstitial cells in tissue engineered heart valvesen_US
dc.typemaster thesisen_US
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