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Michael R. King
Associate Professor
Ph.D. 1999, University of Notre Dame

Room: 2-5752, Medical Center
(585)275-3285
mike_king@urmc.rochester.edu

Website

http://www.bme.rochester.edu/bmeweb/faculty/king.html

Courses

ChE 466 Microhydrodynamics

Research Topics: Dynamics of leukocyte and platelet adhesion; Computational biofluid mechanics

Research Overview: The King laboratory seeks to understand all aspects of the dynamic interactions between blood, circulating cells, and the tissues that they contact. In particular, the balance between hydrodynamic shear forces and chemical adhesive interactions presents the most scientifically interesting aspect of this field currently, as well as being an area with great potential to impact public health through its relevance to cancer, cardiovascular disease, and inflammation. The ultimate goal of our laboratory is a complete, predictive numerical simulation of blood flow that includes all relevant cellular interactions. The surface interactions between cells in suspension or between suspended cells and the vessel wall is where we stand to make the largest contribution to the field, as a rigorous treatment of particulate flow in a biologically realistic setting has never been previously attempted. One of the greatest challenges that we have faced and will continue to address is the need to bridge multiple length scales: from deviation bond lengths measured at tens of nanometers, to micron-sized blood cells, to larger vessels several millimeters in diameter. Continuum rheological models at the artery scale must be matched in a seamless way with the multiparticle adhesive dynamics (MAD) simulation that is able to consider nearfield interactions during cell-cell or cell-wall collisions. We have already succeeded in reconciling bond compliance and kinetics in a cellular-scale calculation. Our research will progress from code development and in vitro experimentation, to later comparison of MAD with experimental animal models, to finally correlating MAD results to patient data.

Major equipment includes a 3-D motorized Olympus IX81 fluorescence microscope, an 18-processor Sun UltraSparc computing cluster, and a new 12-processor AMD Opteron computing cluster.



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