Requirement of prestimulated THP-1 monocytic cells for endothelial cell activation. Involvement of TNFα

Blood Coagulation and Fibrinolysis

Volumn 8, Issue 1, 1997, Pages 39-47

  Roux, M E ^a   Lecoq, D ^a   Meyer, D ^a   Dosne, A M ^a  

^a BICÊTRE HOSPITAL   (France)

Author keywords

endothelial adhesion molecules; monocytic cells; plasminogen activator inhibitor 1; tumor necrosis factor; von Willebrand factor

Indexed keywords

CELL ADHESION MOLECULE; LIPOPOLYSACCHARIDE; NEOMYCIN; PLASMINOGEN ACTIVATOR INHIBITOR 1; TUMOR NECROSIS FACTOR ALPHA; VON WILLEBRAND FACTOR;

ARTICLE; CELL ACTIVATION; CONTROLLED STUDY; ENDOTHELIUM CELL; HUMAN; HUMAN CELL; MONOCYTE; PRIORITY JOURNAL;

EID: 0030902374     PISSN: 09575235     EISSN: None     Source Type: Journal    
DOI: 10.1097/00001721-199701000-00007     Document Type: Article

References (37)

1. Joris I, Zand T, Nunnari JJ, Krolikowski FJ, Majno G. Studies on the pathogenesis of atherosclerosis. I. Adhesion and emigration of mononuclear cells in the aorta of hypercholesterolemic rats. Am J Pathol 1983; 113:341-358.
2. Cybulsky MI, Gimbrone MA. Endothelial expression of a mononuclear leukocyte adhesion molecule during atherogenesis. Science 1991; 251: 788-791.
3. Gerrity RG. The role of the monocyte in atherogenesis. I. Transition of blood born monocyte into foam cells in fatty lesions. Am J Pathol 1981; 103: 181-190.
4. Schwartz CJ, Valente AJ, Sprague EA, et al. Monocyte-macrophage participation in atherogenesis: inflammatory components of pathogenesis. Semin Thromb Hemost 1986; 12: 79-86.
5. Nawroth PP, Handley DA, Esmon CT, Stern DM. Interleukin 1 induces endothelial cell procoagulant while suppressing cell-surface anticoagulant activity. Proc Natl Acad Sci USA 1986; 83: 3460-3464.
6. Scarpati KM, Sadler JE. Regulation of endothelial cell coagulant properties. Modulation of tissue factor, plasminogen activator inhibitors and thrombomodulin by phorbol 12-myristate 13-acetate and tumor necrosis factor. J Biol Chem 1989; 264: 20705-20713.
7. Emeis JJ, Kooistra T. Interleukin 1 and lipolysaccharide induce an inhibitor of tissue type plasminogen activator in vivo and in cultured endothelial cells. J Exp Med 1986; 123: 1260-1266.
8. Dosne A-M, Dubor F, Lutcher F, Parant M, Chedid L. Tumor necrosis factor (TNF) stimulates plasminogen activator inhibitor (PAI) production by endothelial cells and decreases blood fibrinolytic activity in the rat. Thromb Res 1988; 51 (suppl 8):115-122.
9. Van Hinsbergh VWM, Kooistra T, van den Berg EA, Princen HMG, Fiers W, Emeis JJ. Tumor necrosis factor increases the production of plasminogen activator inhibitor in human endothelial cells in vitro and in rats in vivo. Blood 1988; 72: 1467-1473.
10. Bevilacqua MP, Pober JS, Wheeler ME, Cotran RM, Gimbrone MA. Interleukin 1 acts on cultured human vascular endothelium to increase the adhesion of polymorphonuclear leukocytes, monocytes and related leukocyte cell lines. J Clin Invest 1985; 76: 2003-2011.
11. Hakkert BC, Kuijpers TW, Leeuwenberg JF, Van Mourik JA, Roos D. Neutrophil and monocyte adherence to and migration across monolayers of cytokine-activated endothelial cells: the contribution of CD18, ELAM-1, and VLA-4. Blood 1991; 78: 2721-2726.
12. Adams DH, Shaw S. Leukocyte-endothelial interactions and regulation of leukocyte migration. Lancet 1994; 343: 831-836.
13. Erbe DV, Watson SR, Presta LG, et al. P- and E-selectin use common sites for carbohydrate ligand recognition and cell adhesion. J Cell Biol 1993; 121: 1227-1235.
14. Alon R, Kassner PD, Carr MW, Finger EB, Hemler ME, Springer TA. The integrin VLA-4 supports tethering and rolling in flow on VCAM-1. J Cell Biol 1995; 128: 1243-1253.
15. Luscinskas FW, Kansas GS, Ding H, et al. Monocyte rolling, arrest and spreading on IL-4 activated vascular endothelium under flow is mediated via sequential action of L-selectin, β1 integrins and β2 integrins. J Cell Biol 1994; 125: 1417-1427.
16. Beekhuizen H, Corsèl-van Tilburg AJ, Blockland I, van Furth R. Characterization of the adherence of human monocytes to cytokine-stimulated human macrovascular endothelial cells. Immunology 1991; 74: 661-669.
17. Hakkert BC, Rentenaar JM, van Aken WG, Roos D, van Mourik JA. A three-dimensional model system to study the interactions between human leukocytes and endothelial cells. Eur J Immunol 1990; 20: 2775-2781.
18. Whisler RL, Cornwell DG, Proctor KV, Downs E. Bacterial lipopolysaccharide acts on human endothelial cells to enhance the adherence of peripheral blood monocytes. J Lab Clin Med 1989; 114: 708-716.
19. Fan J, Shimokama T, Haraoka S, Tokunaga O, Watanabe T. Monocyte-endothelial cell interactions in vitro, with reference to the influence of interleukin-1 and tumor necrosis factor. Biol Cell 1993; 79: 17-26.
20. Beekhuizen H, van Furth R. Monocyte adherence to human vascular endothelium. J Leukoc Biol 1993; 54: 363-378.
21. Weill D, Wautier J-L, Dosquet C, Wautier M-P, Carreno M-P, Boval B. Monocyte modulation of endothelial leukocyte adhesion molecules. J Lab Clin Med 1995; 125: 768-774.
22. MacKay F, Loetscher H, Stueber D, Gehr G, Lesslauer W. Tumor necrosis factor α (TNF-α)-induced cell adhesion to human endothelial cells is under dominant control of one receptor type, TNF-R55. J Exp Med 1993; 177: 1277-1286.
23. Newman W, Beall LD, Carson CW, Hunder GG, Graben N, Randhawa ZI, Gopal TV, Wiener-Kronish J, Matthay MA. Soluble E-selectin is found in supernatants of activated cells and is elevated in the serum of patients with septic shock. J Immunol 1993; 150: 644-654.
24. Hashemi S, Tackaberry ES, Palmer DS, Rock G, Ganz PR. DDAVP-induced release of von Willebrand factor from endothelial cells in vitro: the effect of plasma and blood cells. Biochim Biophys Acta 1990; 1052: 63-70.
25. Hakkert BC, Rentenaar JM, van Mourik JA. Monocytes enhance endothelial von Willebrand factor release and prostacyclin production with different kinetics and dependency on intercellular contact between these two cell types. Br J Haematol 1992; 80: 495-503.
26. Freshney RI. Culture of Animal Cells. New York: Wiley-Liss, 1987.
27. Deguine V, Kerbiriou-Nabias D, Lecoq D, Greenberg SM, Meyer D, Dosne A-M. Cyclic adenosine monophosphate-dependent mechanisms induce von Willebrand factor expression in the Dami megakaryoblastic cell line. Blood Coag Fibrinol 1995; 6: 42-50.
28. Jonjic N, Jilek P, Bernasconi S, et al. Molecules involved in the adhesion and cytotoxicity of activated monocytes on endothelial cells. J Immunol 1992; 148: 2080-2083.
29. Tsuchiya S, Yamabe M, Yamaguchi Y, Kobayashi Y, Konno T, Tada K. Establishment and characterixation of a human acute leukemia cell line (THP-1). Int J Cancer 1980; 26: 171-176.
30. Dubor F, Dosne A-M, Chedid L. Effect of polymyxin B and colimycin on induction of plasminogen antiactivator by lipopolysaccharide (LPS) in human endothelial cells culture. Infect Immun 1986; 52: 725-729.
31. Dosne A-M, Dubor F, Chedid L. Plasminogen activator inhibitor induced by lipopolysaccharide injection in the rat. Zymographic analysis. Fibrinolysis 1987; 1: 45-49.
32. Hakkert BC, Rentenaar JM, van Mourik JA. Monocytes enhance the bidirectional release of type I plasminogen activator inhibitor by endothelial cells. Blood 1990; 76: 2272-2278.
33. Schindler R, Mancilla J, Endres S, Ghorbani R, Clark SC, Dinarello CA. Correlations and interactions in the production of interleukin-6 (IL-6), IL-1 and tumor necrosis factor (TNF) in human blood mononuclear cells: IL-6 suppresses IL-1 and TNF. Blood 1990; 75: 40-47.
34. Combe C, Duplaa C, Couffinhal T, Moreau C, Bonnet C. Induction of intercellular adhesion molecule-1 by monocyte adhesion to endothelial cells in human culture system. J Cell Physiol 1995; 164: 295-303.
35. Paleolog EM, Crossman DC, McVey JH, Pearson JD. Differential regulation by cytokines of constitutive and stimulated secretion of von Willebrand factor from endothelial cells. Blood 1990; 75: 688-695.
36. DeForge LE, Kenney JS, Jones ML, Warren JS, Remick DG. Biphasic production of IL-8 in lipopolysaccharide (LPS)-stimulated human whole blood. Separation of LPS- and cytokine-stimulated components using antitumor necrosis factor and anti-IL-1 antibodies. J Immunol 1992; 148: 2133-2141.
37. Martin TR, Mongovin SM, Tobias PS, et al. The CD14 differentiation antigen mediates the development of endotoxin responsiveness during differentiation of mononuclear phagocytes. J Leukoc Biol 1994; 56: 1-9.