The objective of this study of blood rheology and hemodynamics in normal and pathological models is a collaborative interdisciplinary effort to characterize the biochemical and physical properties of blood cells, their membranes and adhesive molecules, as these properties have significance to maturation of erythrocytes and leukocytes; contribute to flow behavior in the microcirculation; and as they pertain to microvascular inflammatory response and occlusive phenomena. The efforts focus on the physiological processes of cell maturation and activation, flow in the microvasculature (including cell adhesion to endothelium, and occlusion), and transport of oxygen, and combine the experimental approaches to issues of clinical importance with analytical and theoretical contributions of engineering scientists and biophysicists. Model disorders for study include sickle cell disease, hereditary spherocytosis, diabetes, leukemias and vaso-occlusive disorders. The proposed projects include: (1) Investigations of the interactions of adhesion molecules with blood cell and endothelial cell surfaces, under flow conditions, and the adhesion processes; (2) Studies of the mechanical properties of maturing blood cells and how they affect blood microcirculation; (3) Examination of control mechanisms of microvascular blood flow, including responses to the presence of altered blood cells; (4) Development and utilization of realistic mathematical models of microvascular blood flow; and (5) Extension of model and theoretical studies of studies of microcirculatory flow to provide hydrodynamic bases for interpreting observed cellular interactions. Three core units provide administrative functions, a flow cytometry laboratory service, and a comprehensive image analysis system.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Program Projects (P01)
Project #
5P01HL018208-23
Application #
2445086
Study Section
Heart, Lung, and Blood Research Review Committee B (HLBB)
Project Start
1988-07-01
Project End
1998-06-30
Budget Start
1997-07-01
Budget End
1998-06-30
Support Year
23
Fiscal Year
1997
Total Cost
Indirect Cost
Name
University of Rochester
Department
Biochemistry
Type
Schools of Dentistry
DUNS #
208469486
City
Rochester
State
NY
Country
United States
Zip Code
14627
Vats, Kanika; Marsh, Graham; Harding, Kristen et al. (2017) Nanoscale physicochemical properties of chain- and step-growth polymerized PEG hydrogels affect cell-material interactions. J Biomed Mater Res A 105:1112-1122
Henry, Steven J; Crocker, John C; Hammer, Daniel A (2016) Motile Human Neutrophils Sense Ligand Density Over Their Entire Contact Area. Ann Biomed Eng 44:886-94
Marsh, Graham; Waugh, Richard E (2016) A simple approach for bioactive surface calibration using evanescent waves. J Microsc 262:245-51
Rocheleau, Anne D; Wang, Weiwei; King, Michael R (2016) Effect of Pseudopod Extensions on Neutrophil Hemodynamic Transport Near a Wall. Cell Mol Bioeng 9:85-95
Svetina, Saša; Kokot, Gašper; Kebe, Tjaša Švelc et al. (2016) A novel strain energy relationship for red blood cell membrane skeleton based on spectrin stiffness and its application to micropipette deformation. Biomech Model Mechanobiol 15:745-58
Rocheleau, Anne D; Cao, Thong M; Takitani, Tait et al. (2016) Comparison of human and mouse E-selectin binding to Sialyl-Lewis(x). BMC Struct Biol 16:10
MacKay, Joanna L; Hammer, Daniel A (2016) Stiff substrates enhance monocytic cell capture through E-selectin but not P-selectin. Integr Biol (Camb) 8:62-72
Hind, Laurel E; Lurier, Emily B; Dembo, Micah et al. (2016) Effect of M1-M2 Polarization on the Motility and Traction Stresses of Primary Human Macrophages. Cell Mol Bioeng 9:455-465
Lim, Kihong; Hyun, Young-Min; Lambert-Emo, Kris et al. (2015) Visualization of integrin Mac-1 in vivo. J Immunol Methods 426:120-7
Beste, Michael T; Lomakina, Elena B; Hammer, Daniel A et al. (2015) Immobilized IL-8 Triggers Phagocytosis and Dynamic Changes in Membrane Microtopology in Human Neutrophils. Ann Biomed Eng 43:2207-19

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