This revised FIRST Award application seeks to better understand endothelial cell (EC) adhesion and migration as a function of flow and cytokines. The protein and mRNA expression of endothelial GPIb and VnR will be measured as a function of shear stress in the presence and absence of cytokines tumor necrosis factor alpha and interferon gamma. The relative contribution of EC GPIb/IX and VnR to adhesion and migration will be studied under conditions of variable shear stress and in the presence and absence of cytokines. Finally, the role of the EC cytoskeleton in GPIb/IX-dependent EC adhesion and migration will be studied under conditions of variable shear stress and in the presence and absence of cytokines.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
First Independent Research Support & Transition (FIRST) Awards (R29)
Project #
5R29HL051415-03
Application #
2702237
Study Section
Hematology Subcommittee 2 (HEM)
Project Start
1996-05-01
Project End
2000-04-30
Budget Start
1998-05-01
Budget End
1999-04-30
Support Year
3
Fiscal Year
1998
Total Cost
Indirect Cost
Name
Thomas Jefferson University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
061197161
City
Philadelphia
State
PA
Country
United States
Zip Code
19107
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Cai, G; Lian, J; Shapiro, S S et al. (2000) Evaluation of endothelial cell migration with a novel in vitro assay system. Methods Cell Sci 22:107-14
Beacham, D A; Lian, J; Wu, G et al. (1999) Arterial shear stress stimulates surface expression of the endothelial glycoprotein Ib complex. J Cell Biochem 73:508-21
Lian, J; Guoping, C; Shapiro, S S et al. (1999) Glycoprotein Ibalpha can mediate endothelial cell migration on von Willebrand factor-containing substrata. Exp Cell Res 252:114-22