The objective of this study of blood rheology is a collaborative interdisciplinary effort to characterize the biochemical and physical properties of blood cells and their membranes, and of fibrin, as these properties have significance to release of maturing erythrocytes and leukocytes from marrow; contribute to flow behavior in the microcirculation; and as they pertain to microvascular occlusive phenomena, including fibrin clot formation and thrombolysis. The efforts focus on the physiological processes of marrow egress, flow in microvasculature and in occlusion, and combine the experimental approaches to issues of clinical importance with the analytical and theoretical contributions of engineering scientists and biophysicists. The Core provides administrative, management and advisory functions. Project 1 examines marrow release phenomena; 2, is concerned with fibrin and products in clot production and lysis, and with in vitro studies in flow channels and vessel replicas; 3, studies of erythrocyte membrane protein structure and function; 4, development of methods for measurement of single cell nucleotides and correlation with shape; 5, correlation of erythrocyte and leukocyte membrane properties with capillary flow behavior; 6, investigation of erythrocyte deformability in in vitro flow systems; 7, theoretical mathematical models of transport and particle behavior in capillaries; 8, development of optical imaging methods to enhance cell shape studies; and 9, theoretical and experimental studies of erythrocyte shape and aggregation.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Program Projects (P01)
Project #
5P01HL018208-17
Application #
3097632
Study Section
Heart, Lung, and Blood Research Review Committee B (HLBB)
Project Start
1988-07-01
Project End
1993-06-30
Budget Start
1991-09-01
Budget End
1992-06-30
Support Year
17
Fiscal Year
1991
Total Cost
Indirect Cost
Name
University of Rochester
Department
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
Hind, Laurel E; Dembo, Micah; Hammer, Daniel A (2015) Macrophage motility is driven by frontal-towing with a force magnitude dependent on substrate stiffness. Integr Biol (Camb) 7:447-53
Dominguez, George A; Anderson, Nicholas R; Hammer, Daniel A (2015) The direction of migration of T-lymphocytes under flow depends upon which adhesion receptors are engaged. Integr Biol (Camb) 7:345-55

Showing the most recent 10 out of 249 publications