Perfusion with sickle erythrocytes up-regulates ICAM-1 and VCAM-1 gene expression in cultured human endothelial cells

• Published in: Blood Vol. 95; no. 10; pp. 3232 - 3241
• Main Authors: SHIU, Y.-T, UDDEN, M. M, MCINTIRE, L. V
• Format: Journal Article
• Language: English
• Published: Washington, DC The Americain Society of Hematology 15-05-2000
• Subjects: Anemia, Sickle Cell - complications; Anemias. Hemoglobinopathies; Arterial Occlusive Diseases - etiology; Arterial Occlusive Diseases - pathology; Biological and medical sciences; Cell Adhesion; Cells, Cultured; Diseases of red blood cells; Endothelium, Vascular - pathology; Endothelium, Vascular - physiology; Erythrocytes - pathology; Gene Expression Regulation; Hematologic and hematopoietic diseases; Humans; Intercellular Adhesion Molecule-1 - biosynthesis; Intercellular Adhesion Molecule-1 - genetics; Medical sciences; Vascular Cell Adhesion Molecule-1 - biosynthesis; Vascular Cell Adhesion Molecule-1 - genetics; Human; Hemoglobinopathy; Endothelial cell; Vascular cell adhesion molecule 1; Sickle cell anemia; Intercellular adhesion molecule 1; Cell adhesion molecule; Cell cell interaction; Hemopathy; Gene expression; Genetic disease; Regulation(control); Hemolytic anemia; Genetics; Sickle cell erythrocyte
• ISSN: 0006-4971; 1528-0020
• DOI: 10.1182/blood.v95.10.3232.010k16_3232_3241

Sickle cell anemia is characterized by periodic vasoocclusive crises. Increased adhesion of sickle erythrocytes to vascular endothelium is a possible contributing factor to vasoocclusion. This study determined the effect of sickle erythrocyte perfusion at a venous shear stress level (1 dyne/cm(2)) on endothelial cell (EC) monolayers. Sickle erythrocytes up-regulated intercellular adhesion molecule-1 (ICAM-1) gene expression in cultured human endothelial cells. This was accompanied by increased cell surface expression of ICAM-1 and also elevated release of soluble ICAM-1 molecules. Expression of vascular cell adhesion molecule-1 (VCAM-1) messenger RNA (mRNA) was also strikingly elevated in cultured ECs after exposure to sickle cell perfusion, although increases in membrane-bound and soluble VCAM-1 levels were small. The presence of cytokine interleukin-1beta in the perfusion system enhanced the production of ICAM-1 and VCAM-1 mRNA, cell surface expression, and the concentrations of circulating forms. This is the first demonstration that sickle erythrocytes have direct effects on gene regulation in cultured human ECs under well-defined flow environments. The results suggest that perfusion with sickle erythrocytes increases the expression of cell adhesion molecules on ECs and stimulates the release of soluble cell adhesion molecules, which may serve as indicators of injury and/or activation of endothelial cells. The interactions between sickle red blood flow, inflammatory cytokines, and vascular adhesion events may render sickle cell disease patients vulnerable to vasoocclusive crises.