Respiratory burst of intestinal macrophages in inflammatory bowel disease is mainly caused by CD14+L1+ monocyte derived cells

Gut

Volumn 37, Issue 3, 1995, Pages 367-373

  Rugtveit, J ^a   Haraldsen, G ^a   Hogasen A K ^b   Bakka, A ^b   Brandtzaeg, P ^a   Scott, H ^a  

^a OSLO UNIVERSITY HOSPITAL   (Norway)

^b UNIVERSITY OF OSLO   (Norway)

Author keywords

CD14 antigen; Inflammatory bowel disease; L1 antigen; Macrophages; Reactive oxygen species; Respiratory burst

Indexed keywords

CALGRANULIN; CD14 ANTIGEN; GAMMA INTERFERON; GRANULOCYTE MACROPHAGE COLONY STIMULATING FACTOR; LIPOPOLYSACCHARIDE; OXYGEN RADICAL;

ARTICLE; CELL CULTURE; COLON; CONTROLLED STUDY; ENTERITIS; HUMAN; HUMAN TISSUE; ILEUM; IN VITRO STUDY; INTESTINE MUCOSA; MACROPHAGE; MONOCYTE; PRIORITY JOURNAL; RESPIRATORY BURST;

EID: 0029146381     PISSN: 00175749     EISSN: None     Source Type: Journal    
DOI: 10.1136/gut.37.3.367     Document Type: Article

References (33)

1. Babior BM. The respiratory burst of phagocytes. J Clin Invest 1984; 73 (3): 599-601.
2. Hume DA, Allan W, Hogan PG, Doe WF. Immunohistochemical characterisation of macrophages in human liver and gastrointestinal tract: expression of CD4, HLA-DR, OKM1, and the mature macrophage marker 25F9 in normal and diseased tissue. J Leukoc Biol 1987; 42 (5): 474-84.
3. Selby WS, Janossy G, Mason DY, Jewell DP. Expression of HLA-DR antigens by colonie epithelium in inflammatory bowel disease. Clin Exp Immunol 1983; 53 (3): 614-8.
4. Rugtveit J, Brandtzaeg P, Halstensen T, Fausa O, Scott H. Increased macrophage subset in inflammatory bowel disease: apparent recruitment from peripheral blood monocytes. Gut 1994; 35: 669-74.
5. Mahida YR, Wu KC, Jewell DP. Respiratory burst activity of intestinal macrophages in normal and inflammatory bowel disease. Gut 1989; 30 (10): 1362-70.
6. Hogg N, MacDonald S, Slusarenko M, Beverley PC. Monoclonal antibodies specific for human monocytes, granulocytes and endothelium. Immunology 1984; 53 (4): 753-67.
7. Allison MC, Cornwall S, Poulter LW, Dhillon AP, Pounder RE. Macrophage heterogeneity in normal colonic mucosa and in inflammatory bowel disease. Gut 1988; 29 (11): 1531-8.
8. Brandtzaeg P. Mucosal and glandular distribution of immunoglobulin component. Immunohistochemistry with a cold ethanol-fixation technique. Immunology 1974; 26: 1101-14.
9. Bull DM, Bookman MA. Isolation and functional characterization of human intestinal mucosal lymphoid cells. J Clin Invest 1977; 59: 966-74.
10. Parks D, Bryan V, VT. O, Herzenberg L. Antigen specific identification and cloning of hybridomas with a fluorescence activated cell sorter. Proc Natl Acad Sci USA 1979; 76: 1962.
11. Mahida YR, Wu KC, Jewell DP. Characterization of antigen-presenting activity of intestinal mononuclear cells isolated from normal and inflammatory bowel disease colon and ileum. Immunology 1988; 65 (4): 543-9.
12. Lin HS, Gordon S. Secretion of plasminogen activator by bone marrow-derived mononuclear phagocytes and its enhancement by colony-stimulating factor. J Exp Med 1979; 150 (2): 231-45.
13. Bevilacqua MP, Amrani D, Mosesson MW, Bianco C. Receptors for cold-insoluble globulin (plasma fibronectin) on human monocytes. J Exp Med 1981; 153 (1): 42-60.
14. Lopez M, Marinache C, Canepa S, Chokri M, Scotto F, Bartholeyns J. Autologous lymphocytes prevent the death of monocytes in culture and promote, as do GM-CSF, IL-3 and M-CSF, their differentiation into macrophages. J Immunol Methods 1993; 159: 29-38.
15. Gillies R, Didier N, Denton M. Determination of cell number in monolayer cultures. Anal Biochem 1986; 159: 109-13.
16. Dale I, Brandtzaeg P, Fagerhol MK, Scott H. Distribution of a new myelomonocytic antigen (L1) in human peripheral blood leukocytes. Immunofluorescence and immunoperoxidase staining features in comparison with lysozyme and lactoferrin. Am J Clin Pathol 1985; 84 (1): 24-34.
17. Brandtzaeg P. Conjugates of immunoglobulin G with different fluorochromes. I. Characterization by anionic-exchange chromatography. Scand J Immunol 1973; 2: 273-90.
18. Andreesen R, Mackensen A, Osterholz J, Brugger W, Lohr GW. Microculture assay for human macrophage maturation in vitro. Cell-ELISA analysis of differentiation antigen expression. Int Arch Allergy Appl Immunol 1988; 86 (3): 281-7.
19. Kvale D, Brandtzaeg P, Lovhaug D. Up-regulation of the expression of secretory component and HLA molecules in a human colonie cell line by tumour necrosis factor-alpha and gamma interferon. Scand J Immunol 1988; 28 (3): 351-7.
20. Pick E, Mizel D. Rapid microassays for the measurement of Superoxide and hydrogen peroxide production by macrophages in culture using an automatic enzyme immunoassay reader. J Immunol Methods 1981; 46 (2): 211-26.
21. Ding AH, Nathan CF. Trace levels of bacterial lipopolysaccharide prevent interferon-gamma or tumour necrosis factor-alpha from enhancing mouse peritoneal macrophage respiratory burst capacity. J Immunol 1987; 139 (6): 1971-7.
22. Murray HW, Spitalny GL, Nathan CF. Activation of mouse peritoneal macrophages in vitro and in vivo by interferon-gamma. J Immunol 1985; 134 (3): 1619-22.
23. Johnston RJ, Chadwick DA, Cohn ZA. Priming of macrophages for enhanced oxidative metabolism by exposure to proteolytic enzymes. J Exp Med 1981; 153 (6): 1678-83.
24. Coleman DL, Chodakewitz JA, Bartiss AH, Mellors JW. Granulocyte-macrophage-colony-stimulating factor enhances selective effector functions of tissue derived macrophages. Blood 1988; 72: 573-8.
25. Sullivan GW, Carper HT, Mandell GL. The effect of three human recombinant hematopoietic growth factors (granulocyte-macrophage colony-stimulating factor, granulocyre colony-stimulating factor, and interleukin-3) on phagocyte oxidative activity. Blood 1993; 81 (7): 1863-70.
26. Kharazmi A, Nielsen H, Hovgaard D, Borregaard N, Nissen NI. Modulation of neutrophil and monocyte function by recombinant human granulocyte macrophage colony-stimulating factor in patients with lymphoma. Eur J Clin Invest 1991; 21 (2): 219-24.
27. Nathan CF, Prendergast TJ, Wiebe ME, et al. Activation of human macrophages. Comparison of other cytokines with interferon-gamma. J Exp Med 1984; 160 (2): 600-5.
28. Lepay DA, Nathan CF, Steinman RM, Murray HW, Cohn ZA. Murine Kupffer cells. Mononuclear phagocytes deficient in the generation of reactive oxygen intermediates. J Exp Med 1985; 161 (5): 1079-96.
29. Szefler SJ, Norton CE, Ball B, Gross JM, Aida Y, Pabst MJ. IFN-gamma and LPS overcome glucocorticoid inhibition of priming for Superoxide release in human monocytes. Evidence that secretion of IL-1 and tumor necrosis factor-alpha is not essential for monocyte priming. J Immunol 1989; 142 (11): 3985-92.
30. Nathan CF, Murray HW, Wiebe ME, Rubin BY. Identification of interferon-gamma as the lymphokine that activates human macrophage oxidative metabolism and antimicrobial activity. J Exp Med 1983; 158 (3): 670-89.
31. Pabst MJ, Hedegaard HB, Johnston RJ. Cultured human monocytes require exposure to bacterial products to maintain an optimal oxygen radical response. J Immunol 1982; 128 (1): 123-8.
32. Brandtzaeg P, Dale I, Fagerhol MK. Distribution of a formalin-resistant myelomonocylic antigen (L1) in human tissues. I. Comparison with other leukocyte markers by paired immunofluorescence and immunoenzyme staining. Am J Clin Pathol 1987; 87 (6): 681-99.
33. Ulevitch RJ, Tobias PS. Recognition of endotoxin by cells leading to transmembrane signaling [Review]. Curr Opin Immunol 1994; 6 (1): 125-30.