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dc.contributor.authorSutton, Amandaen_US
dc.date.accessioned2005-04-13en_US
dc.date.accessioned2014-03-14T21:32:46Z
dc.date.available2005-04-13en_US
dc.date.available2014-03-14T21:32:46Z
dc.date.issued2005-02-07en_US
dc.date.submitted2005-04-04en_US
dc.identifier.otheretd-04042005-221914en_US
dc.identifier.urihttp://hdl.handle.net/10919/41889
dc.description.abstractEndothelial cells separate the bloodstream from the underlying tissue and play a crucial role in vascular homeostasis. They also form an important barrier for vascular drug delivery. This thesis contains preliminary studies targeted at understanding the mechanisms of binding and transport across endothelial cells cultured in vitro. Specifically, the first study investigates how the recombinant source of Factor IX (FIX), a blood coagulant protein used in the treatment of Hemophilia B, impacts surface ligand binding (FIX to its specific receptors) to bovine aortic endothelial cells (BAECs). Competitive binding experiments between 125I-FIX and FIX were undertaken to quantify the interaction of recombinant and transgenic FIX with BAECs and human collagen IV and determine if there was a measurable difference in binding affinity. Results indicate limited specific binding of 125I-FIX to BAECs and no binding to human collagen IV. Concrete conclusions were not drawn from this data due to technical issues during the experimental process. The second study investigates insulin-like growth factor-I (IGF-I) transport across both BAEC and MAC-T cells, a mammary epithelial cell line, cultured on tissue culture inserts. IGF-I is a circulatory growth factor implicated in the regulation of cell division and tissue proliferation. Competitive binding experiments between 125I-IGF-I and unlabeled protein (IGF-I, Y60L-IGF-I, a mutant of IGF-I, and IGF Binding Protein-3 (IGFBP-3)) were undertaken to quantify the binding and transport of IGF-I under various experimental conditions. Results confirmed earlier work from the Williamsâ laboratory indicating that 125I-IGF-I transport was enhanced by incubation with its non-receptor-binding analog, Y60L-IGF-I, but cell surface associated 125I-IGF-I was decreased by its presence. Other studies were undertaken but conclusive results could not be drawn.en_US
dc.publisherVirginia Techen_US
dc.relation.haspartas_thesis_041105.pdfen_US
dc.rightsI hereby certify that, if appropriate, I have obtained and attached hereto a written permission statement from the owner(s) of each third party copyrighted matter to be included in my thesis, dissertation, or project report, allowing distribution as specified below. I certify that the version I submitted is the same as that approved by my advisory committee. I hereby grant to Virginia Tech or its agents the non-exclusive license to archive and make accessible, under the conditions specified below, my thesis, dissertation, or project report in whole or in part in all forms of media, now or hereafter known. I retain all other ownership rights to the copyright of the thesis, dissertation or project report. I also retain the right to use in future works (such as articles or books) all or part of this thesis, dissertation, or project report.en_US
dc.subjectInsulin-like Growth Factor-I (IGF-I)en_US
dc.subjectFactor IX (FIX)en_US
dc.subjectMammary Epithelial Cell (Mac-T)en_US
dc.subjectCompetitive Bindingen_US
dc.subjectPulse-Chaseen_US
dc.subjectBovine Aortic Endothelial Cell (BAEC)en_US
dc.titleIn Vitro Binding and Transport Regulation by Endothelial Cells: Preliminary Studies looking at FIX and IGF-Ien_US
dc.typethesisen_US
dc.contributor.departmentChemical Engineeringen_US
thesis.degree.nameMaster of Scienceen_US
thesis.degree.levelmastersen_US
thesis.degree.grantorVirginia Polytechnic Institute and State Universityen_US
dc.contributor.committeechairWilliams, Kimberly Forstenen_US
dc.contributor.committeememberAkers, Robert Michaelen_US
dc.contributor.committeememberGoldstein, Aaron S.en_US
dc.identifier.sourceurlhttp://scholar.lib.vt.edu/theses/available/etd-04042005-221914/en_US


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