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Delphine Dean, Ph.D.

Assistant Professor of Bioengineering
S.B. Electrical Engineering and Computer Science, 2001,
spacer Massachusetts Institute of Technology (MIT)
M.Eng. Electrical Engineering and Computer Science, 2001, MIT
Ph.D. Electrical Engineering and Computer Science, 2005, MIT

Research Interests
Biological Nanomechanics
Cell-Cell and Cell-Matrix Interactions
Computational Modeling
Bioinformatics


Email:
Office: 201-1 Rhodes Research Center
Phone: 864.656.2611
Honors, Awards, and Professional Activities
arrowBiomedical Research Society (BMES) Poster Award, Oct. 2006
arrowMaterials Research Society (MRS) Graduate Student Gold Award Winner, Dec. 2004
arrowWhitaker Foundation Graduate Fellowship, 2002-2004
arrowMIT Bioengineering Undergraduate Research Award, May 1999
Current Research
Cardiac and Stem Cell Mechanics
We are investigating the mechanical properties of cardiac cells and differentiating stem cells separately and in co-culture and on different matrices using a combination of atomic force microscopy (AFM) and modeling techniques. The goal of this research is to determine when differentiating stem cells match the mechanical properties of the native cardiac cells, what factors are most important for the changes in mechanical properties and what signals affect the time course of differentiations.
Cell Mechanics Modeling
The Hertz model, commonly used in literature to describe cell indentation data, is a simple analytical elastic isotropic theoretical model that can be used to extract quantitative measures of cell stiffness from AFM nanoindentation. However, this model does not capture the complex and dynamic mechanical behavior of most cells that are important for cell function. By correlating the levels of the cytoskeletal proteins to the measured mechanical response of different cell types, we can determine which proteins are most important in cell stiffness. Therefore, concurrent with the cell indentation experiments described above, we are developing theoretical models of cardiac and stem cell mechanics. These models will allow us to build a micro- to macro-scale model of cardiac tissue with varying amounts of each cell type.
Cell-Cell Interactions
Cell-cell interactions that form between cardiac cells over time are being directly characterized. The goal of this project is to understand how cellular adherence junctions form and how they change between the different cell types important for cardiac function and repair. Using AFM techniques, we can observe the formation of intercellular adherence junctions in real time.
Recent Publications
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Han, L., Dean, D., Ortiz, C., Grodzinsky, A. J., "Lateral Nanomechanics of Cartilage Aggrecan Macromolecules", in press Biophysical Journal 2006 
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Pirlo, R. K., Dean, D., Knapp, D. R., Gao, B. Z., "Cell Deposition System Based on Laser Guidance", Biotechnology Journal 1(9):1007-1013 (2006)
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Dean, D., Han, L., Grodzinsky, A. J., and Ortiz, C., "Compressive Nanomechanics of Opposing Aggrecan Macromolecules," Journal of Biomechanics 39(14):2555-2565 (2006)
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Vandiver, J., Dean, D., Patel, N., Botelho, C., Best, S., Santos, J., Lopes, M., Bonfield, W., and Ortiz, C., "Silicon addition to hydroxyapatite increases nanoscale electrostatic, van der Waals, and adhesive interactions," Journal of Biomedical Materials Research 78A(2):352-363 (2006)
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Dean, D., Han, L., Ortiz, C., and Grodzinsky, A. J., "Nanoscale Conformation and Compressibility of Cartilage Aggrecan using Microcontact Printing and Atomic Force Microscopy," Macromolecules 38(10); 4047-4049 (2005)
   
Dept. Chair: Dr. Martine LaBerge
Dept. of Bioengineering | 401 Rhodes Research Center | Clemson, SC 29634
Tel: (864) 656-7276 | Fax: (864) 656-4466 |