A key component of many physiological and pathophysiological processes is the adhesion of leukocytes to the endothelium in the fluid dynamic environment of the circulation. This adhesion involves multiple receptor-ligand pairs which may interact simultaneously and in a functionally overlapping fashion. One approach to elucidating the biophysical and molecular mechanisms which govern this complex cascade is to study the interaction of one particular type of leukocyte adhesion molecule with the endothelium in the absence of other adhesive events. We will use such an approach to investigate hypotheses concerning leukocyte adhesion to the endothelium. Specifically, we will coat spherical 10 mum diameter polystyrene microspheres with the leukocyte ligand P-selectin glycoprotein ligand-1 (PSGL-1), the beta2 integrin Mac-1 (CD11b/CD18) or the beta2 integrin LFA-1 (CD11a/CD18). Previous studies have demonstrated that microspheres coated with PSGL-1 qualitatively recreate cellular attachment and rolling on P-selectin. An unresolved issue concerning the PSGL-1 microsphere system (and this approach in general) is the extent to which ligand coated microspheres quantitatively recreate cellular adhesive events.
The first aim will focus on this issue. We will make a detailed quantitative comparison between PSGL-1 mediated microsphere adhesion to P-selectin to that of PSGL-1 mediated neutrophil adhesion to P-selectin. This study will give insight into the cellular and molecular mechanisms which govern attachment and rolling.
The second aim focuses on adhesion mediated by the neutrophil beta2 integrins, Mac-1 and LFA-1. Based on several observations, it is postulated that beta2 integrin-E-selectin but not beta2 integrin - P-selectin molecular interactions can mediate adhesive processes which may be involved in neutrophil adhesion to the endothelium. To explore this hypothesis, the adhesion of Mac-1 and LFA-1 coated microspheres to E- and P-selectin under in vitro flow attachment and detachment conditions will be studied to determine if beta2 integrin- E-selectin and/or beta2 integrin - P-selectin molecular interactions can mediate adhesive processes.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Academic Research Enhancement Awards (AREA) (R15)
Project #
1R15GM057640-01A1
Application #
2727313
Study Section
Special Emphasis Panel (ZRG3-PBC (01))
Project Start
1999-05-01
Project End
1999-12-31
Budget Start
1999-05-01
Budget End
1999-12-31
Support Year
1
Fiscal Year
1999
Total Cost
Indirect Cost
Name
University of Memphis
Department
Biomedical Engineering
Type
Schools of Engineering
DUNS #
City
Memphis
State
TN
Country
United States
Zip Code
38152
Kummitha, China Malakondaiah; Shirure, Venktesh S; Delgadillo, Luis F et al. (2012) HECA-452 is a non-function blocking antibody for isolated sialyl Lewis x adhesion to endothelial expressed E-selectin under flow conditions. J Immunol Methods 384:43-50
Benavides, Uruguaysito; Gonzalez-Murguiondo, Mariana; Harii, Norikazu et al. (2010) Phenyl methimazole suppresses dextran sulfate sodium-induced murine colitis. Eur J Pharmacol 643:129-38