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Meredith Beckenhaupt Biomedical Engineering, Junior Cameron Ingram Biomedical Engineering, Sophomore Project 1: Self-Assembling Peptide Nanoscaffold for MMP Delivery and Cardiac Regeneration in the Diabetic Heart Dr. Daria Narmoneva Biomedical Engineering, FM Jennifer Hurley Biomedical Engineering, GRA
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Background Information Diabetic cardiomyopathy – Circulatory defects – Impaired heart muscle contraction – Cardiac fibrosis Cardiac Fibrosis – Too much collagen, not enough matrix matalloproteinase (MMP) Possible Treatment Explored: MMP delivery using nanoscaffold
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Goals & Objectives Demonstrate that increased MMP-2 concentration will enhance remodeling of cardiac tissue, in vitro – Cell culture techniques – Methods of quantitative analysis on cell culture, such as ELISA, zymography, histochemistry, and rheometry – Methods of statistical analysis
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Research Tasks Culture cells for certain lengths of time using nanoscaffold, MMP and nanoscaffold, and matrigel Perform testing in order to analyze effectiveness of MMP and nanoscaffold – Protein isolation and ELISA testing – Histological sample preparation and study – Live/Dead preparation and study – Zymography preparation and testing – Rheological preparation and testing Paper writing, abstract and manuscript preparation
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Current Accomplishments Most samples already prepared for protein isolation, and then ELIZA testing Isolating proteins from samples of media – Days 1, 6, 14 – Nanoscaffold, MMP & nanoscaffold, matrigel (control) Started making histology samples and performing microscopy analysis Started live/dead counting for samples at days 1, 6, 14
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Resources Narmoneva, D. A., PhD, Vukmirovic, R., MS, Davis, M. E., PhD, Kamm, R. D., PhD, & Lee, R. T., MD. (2004). Endothelial cells promote cardiac myocyte survival and spatial reorganization. Circulation, 2004(110), 962-968. Segers, V. F.M., & Lee, R. T. (2007). Local delivery of proteins and the use of self-assembling peptides. Drug Discovery Today, 12(13/14), 561-568 Linthout, S. v., Seeland, U., Riad, A., Eckhardt, O., & Hohl, M. (2008). Reduced mmp-2 activity contributes to cardiac fibrosis in experimental diabetic cardiomyopathy. Basic Reseach in Cardiology, 2008(103), 319-327. Hurley, J. R., Balaji, S., & Narmoneva, D. A. (2010). Complex temporal regulation of capillary morphogenesis by fibroblasts. American Journal of Physiology - Cell Physiology, 2010(299), 444-453. Hurley, J. R., & Narmoneva, D. A. (2010, April). Project 1: self-assembling peptide nanoscaffold for mmp delivery and cardiac regeneration in the diabetic heart. Retrieved from http://www.eng.uc.edu/reu/academic/2010- 2011/pages/projects/project1.html
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