Gene Expression of Endothelial Cells due to Interleukin-1 Beta Stimulation and Neutrophil Transmigration

REFERENCES

• Abbassi O., Kishimoto T. K., McIntire L. V., Anderson D. C., Smith C. W. E-selectin supports neutrophil rolling in vitro under conditions of flow. Journal of Clinical Investigation 1993; 92: 2719–2730
   PubMed Web of Science ®Google Scholar
• Abe T., Sugano E., Saigo Y., Tamai M. Interleukin-1beta and barrier function of retinal pigment epithelial cells (arpe-19): Aberrant expression of junctional complex molecules. Investigative Ophthalmology and Visual Science 2003; 44: 4097–4104
   PubMed Web of Science ®Google Scholar
• Baggiolini M., Walz A., Kunkel S. L. Neutrophil-activating peptide-1/interleukin 8, a novel cytokine that activates neutrophils. Journal of Clinical Investigation 1989; 84: 1045–1049
   PubMed Web of Science ®Google Scholar
• Bandman O., Coleman R. T., Loring J. F., Seilhamer J. J., Cocks B. G. Complexity of inflammatory responses in endothelial cells and vascular smooth muscle cells determined by microarray analysis. Annals of the New York Academy of Sciences 2002; 975: 77–90
   PubMed Web of Science ®Google Scholar
• Bazzoni G. Endothelial tight junctions: Permeable barriers of the vessel wall. Thrombosis and Haemostasis 2006; 95: 36–42
   PubMed Web of Science ®Google Scholar
• Brown Z., Gerritsen M. E., Carley W. W., Strieter R. M., Kunkel S. L., Westwick J. Chemokine gene expression and secretion by cytokine-activated human microvascular endothelial cells. Differential regulation of monocyte chemoattractant protein-1 and interleukin-8 in response to interferon-gamma. American Journal of Pathology 1994; 145: 913–921
   PubMed Web of Science ®Google Scholar
• Burke-Gaffney A., Keenan A. K. Modulation of human endothelial cell permeability by combinations of the cytokines interleukin-1 alpha/beta, tumor necrosis factor-alpha and interferon-gamma. Immunopharmacology 1993; 25: 1–9
   PubMed Web of Science ®Google Scholar
• Cepinskas G., Savickiene J., Ionescu C. V., Kvietys P. R. Pmn transendothelial migration decreases nuclear nfkappab in IL-1beta-activated endothelial cells: Role of pecam-1. Journal of Cell Biology 2003; 161: 641–651
   PubMed Web of Science ®Google Scholar
• Cozzolino F., Torcia M., Aldinucci D., Ziche M., Almerigogna F., Bani D., et al. Interleukin 1 is an autocrine regulator of human endothelial cell growth. Proceedings of the National Academy of Sciences of the United States of America 1990; 87: 6487–6491
   PubMed Web of Science ®Google Scholar
• Dennis G., Jr., Sherman B. T., Hosack D. A., Yang J., Gao W., Lane H. C., et al. David: Database for annotation, visualization, and integrated discovery. Genome Biol 2003; 4: P3
   PubMed Web of Science ®Google Scholar
• Dinarello C. A. Biologic basis for interleukin-1 in disease. Blood 1996; 87: 2095–2147
   PubMed Web of Science ®Google Scholar
• Duffy H. S., John G. R., Lee S. C., Brosnan C. F., Spray D. C. Reciprocal regulation of the junctional proteins claudin-1 and connexin43 by interleukin-1beta in primary human fetal astrocytes. Journal of Neuroscience 2000; 20: RC114, (1–6)
   PubMed Web of Science ®Google Scholar
• Dunne A., O'Neill L. A. The interleukin-1 receptor/toll-like receptor superfamily: Signaltransduction during inflammation and host defense. Sci Science's Signal Transduction Knowledge Environment 2003; re3, 2003
   Google Scholar
• Etienne S., Adamson P., Greenwood J., Strosberg A. D., Cazaubon S., Couraud P. O. ICAM-1 signaling pathways associated with rho activation in microvascular brain endothelial cells. Journal of Immunology 1998; 161: 5755–5761
   PubMed Web of Science ®Google Scholar
• Fontijn R. D., Rohlena J., van Marle J., Pannekoek H., Horrevoets A. J. Limited contribution of claudin-5-dependent tight junction strands to endothelial barrier function. European Journal of Cell Biology 2006; 85: 1131–1144
   PubMed Web of Science ®Google Scholar
• Frye S. R., Yee A., Eskin S. G., Guerra R., Cong X., McIntire L. V. Cdna microarray analysis of endothelial cells subjected to cyclic mechanical strain: Importance of motion control. Physiology and Genomics 2005; 21: 124–130
   PubMed Web of Science ®Google Scholar
• Hentzen E., McDonough D., McIntire L., Smith C. W., Goldsmith H. L., Simon S. I. Hydrodynamic shear and tethering through e-selectin signals phosphorylation of p38 map kinase and adhesion of human neutrophils. Annals of Biomedical Engineering 2002; 30: 987–1001
   PubMed Web of Science ®Google Scholar
• Hentzen E. R., Neelamegham S., Kansas G. S., Benanti J. A., McIntire L. V., Smith C. W., et al. Sequential binding of cd11a/cd18 and cd11b/cd18 defines neutrophil capture and stable adhesion to intercellular adhesion molecule-1. Blood 2000; 95: 911–920
   PubMed Web of Science ®Google Scholar
• Herrmann J., Lerman L. O., Lerman A. Ubiquitin and ubiquitin-like proteins in protein regulation. Circulation Research 2007; 100: 1276–1291
   PubMed Web of Science ®Google Scholar
• Huang A. J., Manning J. E., Bandak T. M., Ratau M. C., Hanser K. R., Silverstein S. C. Endothelial cell cytosolic free calcium regulates neutrophil migration across monolayers of endothelial cells. Journal of Cell Biology 1993; 120: 1371–1380
   PubMed Web of Science ®Google Scholar
• Jones D. A., Abbassi O., McIntire L. V., McEver R. P., Smith C. W. P-selectin mediates neutrophil rolling on histamine-stimulated endothelial cells. Biophysical Journal 1993; 65: 1560–1569
   PubMed Web of Science ®Google Scholar
• Karin M., Lin A. Nf-kappab at the crossroads of life and death. Nature Immunology 2002; 3: 221–227
   PubMed Web of Science ®Google Scholar
• Lawrence M. B., Smith C. W., Eskin S. G., McIntire L. V. Effect of venous shear stress on cd18-mediated neutrophil adhesion to cultured endothelium. Blood 1990; 75: 227–237
   PubMed Web of Science ®Google Scholar
• Lee K. Y., Ito K., Hayashi R., Jazrawi E. P., Barnes P. J., Adcock I. M. Nf-kappab and activator protein 1 response elements and the role of histone modifications in il-1beta-induced tgf-beta1 gene transcription. Journal of Immunology 2006; 176: 603–615
   PubMed Web of Science ®Google Scholar
• Marcus B. C., Hynes K. L., Gewertz B. L. Loss of endothelial barrier function requires neutrophil adhesion. Surgery 1997; 122: 420–426, discussion 426–427
   PubMed Web of Science ®Google Scholar
• Marcus B. C., Wyble C. W., Hynes K. L., Gewertz B. L. Cytokine-induced increases in endothelial permeability occur after adhesion molecule expression. Surgery 1996; 120: 411–416, discussion 416–417
   PubMed Web of Science ®Google Scholar
• Mayer H., Bilban M., Kurtev V., Gruber F., Wagner O., Binder B. R., et al. Deciphering regulatory patterns of inflammatory gene expression from interleukin-1-stimulated human endothelial cells. Arteriosclerosis, Thrombosis, and Vascular Biology 2004; 24: 1192–1198
   PubMed Web of Science ®Google Scholar
• McCormick S. M., Eskin S. G., McIntire L. V., Teng C. L., Lu C. M., Russell C. G., et al. DNA microarray reveals changes in gene expression of shear stressed human umbilical vein endothelial cells. Proceedings of the National Academy of Sciences of the United States of America 2001; 98: 8955–8960
   PubMed Web of Science ®Google Scholar
• Molony L., Armstrong L. Cytoskeletal reorganizations in human umbilical vein endothelial cells as a result of cytokine exposure. Experimental Cell Research 1991; 196: 40–48
   PubMed Web of Science ®Google Scholar
• Montesano R., Orci L., Vassalli P. Human endothelial cell cultures: Phenotypic modulation by leukocyte interleukins. Journal of Cellular Physiology 1985; 122: 424–434
   PubMed Web of Science ®Google Scholar
• Naldini A., Carraro F. Role of inflammatory mediators in angiogenesis. Current Drug Targets, Inflammation, and Allergy 2005; 4: 3–8
   PubMedGoogle Scholar
• Nemeth E., Tashima L. S., Yu Z., Bryant-Greenwood G. D. Fetal membrane distention: I. Differentially expressed genes regulated by acute distention in amniotic epithelial (wish) cells. American Journal of Obstetrics and Gynecology 2000; 182: 50–59
   PubMed Web of Science ®Google Scholar
• Nitta T., Hata M., Gotoh S., Seo Y., Sasaki H., Hashimoto N., et al. Size-selective loosening of the blood-brain barrier in claudin-5-deficient mice. Journal of Cell Biology 2003; 161: 653–660
   PubMed Web of Science ®Google Scholar
• Ognjanovic S., Bao S., Yamamoto S. Y., Garibay-Tupas J., Samal B., Bryant-Greenwood G. D. Genomic organization of the gene coding for human pre-B-cell colony enhancing factor and expression in human fetal membranes. Journal of Molecular Endocrinology 2001; 26: 107–117
   PubMed Web of Science ®Google Scholar
• Ognjanovic S., Ku T. L., Bryant-Greenwood G. D. Pre-B-cell colony-enhancing factor is a secreted cytokine-like protein from the human amniotic epithelium. American Journal of Obstetrics and Gynecology 2005; 193: 273–282
   PubMed Web of Science ®Google Scholar
• Ostermann G., Weber K. S., Zernecke A., Schroder A., Weber C. Jam-1 is a ligand of the beta(2) integrin lfa-1 involved in transendothelial migration of leukocytes. Nature Immunology 2002; 3: 151–158
   PubMed Web of Science ®Google Scholar
• Ott L. W., Resing K. A., Sizemore A. W., Heyen J. W., Cocklin R. R., Pedrick N. M., et al. Tumor necrosis factor-alpha- and interleukin-1-induced cellular responses: Coupling proteomic and genomic information. Journal of Proteome Research 2007; 6: 2176–2185
   PubMed Web of Science ®Google Scholar
• Rao R. M., Yang L., Garcia-Cardena G., Luscinskas F. W. Endothelial-dependent mechanisms of leukocyte recruitment to the vascular wall. Circulation Research 2007; 101: 234–247
   PubMed Web of Science ®Google Scholar
• Schenkel A. R., Mamdouh Z., Chen X., Liebman R. M., Muller W. A. Cd99 plays a major role in the migration of monocytes through endothelial junctions. Nature Immunology 2002; 3: 143–150
   PubMed Web of Science ®Google Scholar
• Schenkel A. R., Mamdouh Z., Muller W. A. Locomotion of monocytes on endothelium is a critical step during extravasation. Nature Immunology 2004; 5: 393–400
   PubMed Web of Science ®Google Scholar
• Scholz D., Devaux B., Hirche A., Potzsch B., Kropp B., Schaper W., et al. Expression of adhesion molecules is specific and time-dependent in cytokine-stimulated endothelial cells in culture. Cell and Tissue Research 1996; 284: 415–423
   PubMed Web of Science ®Google Scholar
• Schulz C., Schafer A., Stolla M., Kerstan S., Lorenz M., von Bruhl M. L., et al. Chemokine fractalkine mediates leukocyte recruitment to inflammatory endothelial cells in flowing whole blood: A critical role for P-selectin expressed on activated platelets. Circulation 2007; 116: 764–773
   PubMed Web of Science ®Google Scholar
• Skop B., Sobczak A., Drozdz M., Kotrys-Puchalska E. Comparison of the action of transforming growth factor-beta 1 and interleukin-1 beta on matrix metabolism in the culture of porcine endothelial cells. Biochimie 1996; 78: 103–107
   PubMed Web of Science ®Google Scholar
• Smith W. L., DeWitt D. L., Garavito R. M. Cyclooxygenases: Structural, cellular, and molecular biology. Annual Review of Biochemistry 2000; 69: 145–182
   PubMed Web of Science ®Google Scholar
• Springer T. A. Traffic signals for lymphocyte recirculation and leukocyte emigration: The multistep paradigm. Cell 1994; 76: 301–314
   PubMed Web of Science ®Google Scholar
• Tesfamariam B., DeFelice A. F. Endothelial injury in the initiation and progression of vascular disorders. Vascular Pharmacology 2007; 46: 229–237
   PubMed Web of Science ®Google Scholar
• van Buul J. D., Hordijk P. L. Signaling in leukocyte transendothelial migration. Arteriosclerosis, Thrombosis, and Vascular Biology 2004; 24: 824–833
   PubMed Web of Science ®Google Scholar
• van Wetering S., van den Berk N., van Buul J. D., Mul F. P., Lommerse I., Mous R., et al. VCAM-1-mediated rac signaling controls endothelial cell-cell contacts and leukocyte transmigration. American Journal of Physiology Cellular Physiology 2003; 285: C343–352
   PubMed Web of Science ®Google Scholar
• Vestweber D. Adhesion and signaling molecules controlling the transmigration of leukocytes through endothelium. Immunological Reviews 2007; 218: 178–196
   PubMed Web of Science ®Google Scholar
• Winn R. K., Harlan J. M. The role of endothelial cell apoptosis in inflammatory and immune diseases. Journal of Thrombosis and Haemostasis 2005; 3: 1815–1824
   PubMed Web of Science ®Google Scholar
• Ye S. Q., Zhang L. Q., Adyshev D., Usatyuk P. V., Garcia A. N., Lavoie T. L., et al. Pre-B-cell-colony-enhancing factor is critically involved in thrombin-induced lung endothelial cell barrier dysregulation. Microvascular Research 2005; 70: 142–151
   PubMed Web of Science ®Google Scholar
• Yee A., Sakurai Y., Eskin S. G., McIntire L. V. A validated system for simulating common carotid arterial flow in vitro: Alteration of endothelial cell response. Annals of Biomedical Engineering 2006; 34: 593–604
   PubMed Web of Science ®Google Scholar
• Zhao B., Stavchansky S. A., Bowden R. A., Bowman P. D. Effect of interleukin-1beta and tumor necrosis factor-alpha on gene expression in human endothelial cells. American Journal of Physiology Cellular Physiology 2003; 284: C1577–C1583
   PubMed Web of Science ®Google Scholar
• Zimmerman G. A., McIntyre T. M., Prescott S. M. Thrombin stimulates the adherence of neutrophils to human endothelial cells in vitro. Journal of Clinical Investigation 1985; 76: 2235–2246
   PubMed Web of Science ®Google Scholar