Cell adhesion molecules in coronary artery disease
Y Jang,
AM Lincoff,
EF Plow,
and
EJ Topol
Center for Thrombosis and Vascular Biology, Cleveland, Ohio.
To date, six families of cell adhesion molecules are known. These are cell surface receptors that mediate adhesion of cells to each other or to components of the extracellular matrix and include integrins, selectins, the immunoglobulin superfamily, cadherins, proteoglycans and mucins. These cell adhesion molecules play a key role in cell-cell interaction (such as among endothelium, monocytes, smooth muscle cells and platelets) and cell-extracellular matrix interaction (such as between leukocytes, platelets or fibroblasts and the extracellular matrix). The importance of these interactions has recently been demonstrated in clinical trials with the use of an antibody fragment directed against the platelet alpha IIb beta IIIa integrin, with reduction of arterial thrombosis and restenosis after percutaneous coronary interventions. A fundamental role for cell adhesion molecules has been suggested for several other relevant disease processes, including atherosclerosis, acute coronary syndromes, reperfusion injury and allograft vasculopathy. This review focuses on providing the clinically relevant biology of these families of adhesion molecules, setting the foundation for delineation of their emerging role in cardiovascular therapeutics.
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[Abstract]
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T. Ueyama, H. Ikeda, N. Haramaki, K. Kuwano, and T. Imaizumi
Effects of Monoclonal Antibody to P-Selectin and Analogue of Sialyl Lewis X on Cyclic Flow Variations in Stenosed and Endothelium-Injured Canine Coronary Arteries
Circulation,
March 18, 1997;
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[Abstract]
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P.H.M. Kuijper, H.I. G. Torres, J.A.M. van der Linden, J.-W.J. Lammers, J.J. Sixma, J.J. Zwaginga, and L. Koenderman
Neutrophil Adhesion to Fibrinogen and Fibrin Under Flow Conditions Is Diminished by Activation and L-Selectin Shedding
Blood,
March 15, 1997;
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[Abstract]
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M. R. Adams, W. Jessup, D. Hailstones, and D. S. Celermajer
L-Arginine Reduces Human Monocyte Adhesion to Vascular Endothelium and Endothelial Expression of Cell Adhesion Molecules
Circulation,
February 4, 1997;
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M Sandig, E Negrou, and K. Rogers
Changes in the distribution of LFA-1, catenins, and F-actin during transendothelial migration of monocytes in culture
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A. L. Catapano
Antioxidant Effect of Flavonoids
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[Abstract]
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D. M. Brown, N. M. Kania, E. T. Choi, L. A. Lantieri, E. N. Pasia, T.-C. Wun, and R. K. Khouri
Local Irrigation With Tissue Factor Pathway Inhibitor Inhibits Intimal Hyperplasia Induced by Arterial Interventions
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[Abstract]
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E. J. Weiss, P. F. Bray, M. Tayback, S. P. Schulman, T. S. Kickler, L. C. Becker, J. L. Weiss, G. Gerstenblith, and P. J. Goldschmidt-Clermont
A Polymorphism of a Platelet Glycoprotein Receptor as an Inherited Risk Factor for Coronary Thrombosis
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[Abstract]
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H. Ikeda, Y. Takajo, K. Ichiki, T. Ueno, S. Maki, T. Noda, K. Sugi, and T. Imaizumi
Increased Soluble Form of P-Selectin in Patients With Unstable Angina
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October 1, 1995;
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[Abstract]
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J. Lefkovits, E. F. Plow, and E. J. Topol
Platelet Glycoprotein IIb/IIIa Receptors in Cardiovascular Medicine
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B. Yan and J. W. Smith
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[Abstract]
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L. Calabresi, M. Gomaraschi, B. Villa, L. Omoboni, C. Dmitrieff, and G. Franceschini
Elevated Soluble Cellular Adhesion Molecules in Subjects With Low HDL-Cholesterol
Arterioscler Thromb Vasc Biol,
April 1, 2002;
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656 - 661.
[Abstract]
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P. Ziccardi, F. Nappo, G. Giugliano, K. Esposito, R. Marfella, M. Cioffi, F. D'Andrea, A. M. Molinari, and D. Giugliano
Reduction of Inflammatory Cytokine Concentrations and Improvement of Endothelial Functions in Obese Women After Weight Loss Over One Year
Circulation,
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105(7):
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[Abstract]
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A. Jager, V. W.M. van Hinsbergh, P. J. Kostense, J. J. Emeis, G. Nijpels, J. M. Dekker, R. J. Heine, L. M. Bouter, and C. D.A. Stehouwer
C-Reactive Protein and Soluble Vascular Cell Adhesion Molecule-1 Are Associated With Elevated Urinary Albumin Excretion but Do Not Explain Its Link With Cardiovascular Risk
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22(4):
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[Abstract]
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