Regulatory role of DC-derived osteopontin in systemic allergen sensitization

European Journal of Immunology

Volumn 39, Issue 12, 2009, Pages 3323-3330

  Kurokawa, Masatsugu ^a,b   Konno, Satoshi ^a,c   Takahashi, Ayumu ^c   Plunkett, Beverly ^a   Rittling, Susan R ^d   Matsui, Yutaka ^e   Kon, Shigeyuki ^e   Morimoto, Junko ^e   Uede, Toshimitsu ^e   Matsukura, Satoshi ^b   Kokubu, Fumio ^f   Adachi, Mitsuru ^b   Nishimura, Masaharu ^c   Huang, Shau Ku ^a  

^a JOHNS HOPKINS ASTHMA AND ALLERGY CENTER   (United States)

^b SHOWA UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^c HOKKAIDO UNIVERSITY   (Japan)

^d RUTGERS UNIVERSITY   (United States)

^e HOKKAIDO UNIVERSITY   (Japan)

^f SHOWA UNIVERSITY FUJIGAOKA HOSPITAL   (Japan)

Author keywords

Bone marrow derived DC; IgE; Osteopontin; Th2 cytokines

Indexed keywords

CD4 ANTIGEN; ESCHERICHIA COLI LIPOPOLYSACCHARIDE; IMMUNOGLOBULIN E; INTERLEUKIN 12; INTERLEUKIN 12P70; INTERLEUKIN 13; OSTEOPONTIN; OVALBUMIN;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; CD4+ T LYMPHOCYTE; CELL CULTURE; CONTROLLED STUDY; CYTOKINE PRODUCTION; DENDRITIC CELL; HYPERSENSITIVITY; IMMUNOGLOBULIN PRODUCTION; IMMUNOREGULATION; IN VIVO STUDY; MOUSE; NONHUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN FUNCTION; TH2 CELL; WILD TYPE;

ADOPTIVE TRANSFER; ALLERGENS; ANIMALS; BRONCHIAL HYPERREACTIVITY; CD4-POSITIVE T-LYMPHOCYTES; DENDRITIC CELLS; ENZYME-LINKED IMMUNOSORBENT ASSAY; IMMUNOGLOBULIN E; IMMUNOGLOBULIN G; INTERFERON-GAMMA; INTERLEUKIN-12; INTERLEUKIN-13; LIPOPOLYSACCHARIDES; MICE; MICE, INBRED BALB C; MICE, INBRED C57BL; MICE, KNOCKOUT; OSTEOPONTIN; OVALBUMIN; RECOMBINANT PROTEINS;

EID: 73249129192     PISSN: 00142980     EISSN: 15214141     Source Type: Journal    
DOI: 10.1002/eji.200838970     Document Type: Article

References (40)

1. Rittling, S. and Denhardt, D. T., Osteopontin function in pathology: lessons from osteopontin-deficient mice. Exp. Nephrol. 1999. 7: 103-113.
2. O'Regan, A. W., Nau, G. J., Chupp, G. L. and Berman, J. S., Osteopontin (Eta-I) in cell-mediated immunity: teaching an old dog new tricks. Immunol. Today 2000. 21: 475-478.
3. Uede, T., Katagiri, Y., Iizuka, J. and Murakami, M., Osteopontin, a coordinator of host defense system: a cytokine or an extracellular adhesive protein? Microbiol. Immunol. 1997. 41: 641-648.
4. Denhardt, D. T., Noda, M., O'Regan, A. W., Palvin, D. and Berman, J. S., Osteopontin as a means to cope with environmental insults: regulation of inflammation, tissue remodeling, and cell survival. J. Clin. Invest. 2001. 107: 1055-1061.
5. Yamamoto, N., Sakai, F., Kon, S., Morimoto, J., Kimura, C., Yamazaki, H., Okazaki, I. et al., Essential role of the cryptic epitope SLAYGLR within osteopontin in a murine model of rheumatoid arthritis. J. Clin. Invest. 2003. 112: 181-188.
6. Ishii, T., Ohshima, S., Ishida, T., Mima, T., Tabunoki, Y., Kobayashi, H., Maeda, M. et al., Osteopontin as a positive regulator in the osteoclastogenesis of arthritis. Biochem. Biophys. Res. Commun. 2004. 316: 809-815.
7. O'Regan, A.W., Hayden, J.M., Body, S., Liaw, L., Mulligan, N., Goetschkes, M. and Berman, J. S., Abnormal pulmonary granuloma formation in osteopontin-deficient mice. Am. J. Respir. Crit. Care Med. 2001. 164: 2243-2247.
8. Chabas, D., Baranzini, S. E., Mitchell, D., Bernard, C. C., Rittling, S. R., Denhardt, D. T., Sobel, R. A. et al., The influence of the proinflammatory cytokine, osteopontin, on autoimmune demyelinating disease. Science 2001. 294: 1731-1735.
9. O'Regan, A. W., Chupp, G. L., Lowry, J. A., Goetschkes, M., Mulligan, N. and Berman, J. S., Osteopontin is associated with T cells in sarcoid granulomas and has T cell adhesive and cytokine-like properties in vitro. J. Immunol. 1991. 162: 1024-1031.
10. Koguchi, Y., Kawakami, K., Uezu, K., Fukushima, K., Kon, S., Maeda, M., Nakamoto, A. et al., High plasma osteopontin level and its relationship with interleukin-12-mediated type 1T helper cell response in tuberculosis. Am. J. Respir. Crit. Care Med. 2003. 167: 1355-1359.
11. Xu, G., Nie, H., Li, N., Zheng, W., Zhang, D., Feng, G., Ni, L. et al., Role of osteopontin in amplification and perpetuation of rheumatoid synovitis. J. Clin. Invest. 2005. 115: 1060-1067.
12. Sato, T., Nakai, T., Tamura, N., Okamoto, S., Matsuoka, K., Sakuraba, A., Fukushima, T. et al., Osteopontin/Eta-1 upregulated in Crohn's disease regulates the Th1 immune response. Gut 2005. 54: 1254-1262.
13. Comabella, M., Pericot, I., Goertsches, R., Nos, C., Castillo, M., Blas Navarro, J., Río, J. et al., Plasma osteopontin levels in multiple sclerosis. J. Neuroimmunol. 2005. 158: 231-239.
14. Ishii, T., Ohshima, S., Ishida, T., Kawase, I., Mima, T., Tabunoki, Y., Kobayashi, H. et al., Mice with osteopontin deletion remain predisposed to collagen-induced arthritis. Arthritis Rheum. 2004. 50: 669-671.
15. Blom, T., Franzen, A., Heinegard, D., Holmdahl, R., Comment on "The influence of the proinflammatory cytokine, osteopontin, on autoimmune demyelinating disease". Science 2003. 299: 1845.
16. Xanthou, G., Alissafi, T., Semitekolou, M., Simoes, D. C., Economidou, E., Gaga, M., Lambrecht, B. N. et al., Osteopontin has a crucial role in allergic airway disease through regulation of dendritic cell subsets. Nat. Med. 2007. 13: 570-578.
17. Takahashi, A., Kurokawa, M., Konno, S., Ito, K., Kon, S., Ashino, S., Nishimura, T. et al., Osteopontin is involved in migration of eosinophils in asthma. Clin. Exp. Allergy 2009. 39: 1152-1159.
18. Nagasaka, A., Matsue, H., Matsushima, H., Aoki, R., Nakamura, Y., Kambe, N., Kon, S. et al., Osteopontin is produced by mast cells and affects IgE-mediated degranulation and migration of mast cells. Eur. J. Immunol. 2008. 38: 489-499.
19. Konno, S., Golden, D. B. K., Schroeder, J., Hamilton, R. G., Lichtenstein, L. M. and Huang, S. K., Increased expression of osteopontin is associated with long-term bee venom immunotherapy. J. Allergy. Clin. Immunol. 2005. 115: 1063-1067.
20. Konno, S., Golden, D. B. K., Schroeder, J., Hamilton, R. G., Lichtenstein, L. M. and Huang, S. K., Level of osteopontin is increased after bee venom immunotherapy. J. Allergy. Clin. Immunol. 2005. 115: 1317-1318.
21. Li, X., O'Regan, A. W. and Berman, J. S., IFN-g induction of osteopontin expression in human monocytoid cells. J. Interferon Cytokine Res. 2003. 23: 259-265.
22. Konno, S., Eckman, J. A., Plunkett, B., Li, X., Berman, J. S., Schroeder, J. and Huang, S. K., Interleukin-10 and Th2 cytokines differentially regulate osteopontin expression in human monocytes and dendritic cells. J. Interferon Cytokine Res. 2006. 26: 562-567.
23. Lambrecht, B. N. and Hammad, H., The other cells in asthma: dendritic cell and epithelial cell crosstalk. Curr. Opin. Pulm. Med. 2003. 9: 34-41.
24. MacDonald, A. S., Straw, A. D., Bauman, B. and Pearce, E. J., CD8-dendritic cell activation status plays an integral role in influencing Th2 response development. J. Immunol. 2001. 167: 1982-1988.
25. Cervi, L., MacDonald, A. S., Kane, C., Dzierszinski, F. and Pearce, E. J., Cutting edge: dendritic cells copulsed with microbial and helminth antigens undergo modified maturation, segregate the antigens to distinct intracellular compartments, and concurrently induce microbe-specific Th1 and helminth-specific Th2 responses. J. Immunol. 2004. 172: 2016-2020.
26. Chen, Z., Gordon, J. R., Zhang, X. and Xiang, J., Analysis of the gene expression profiles of immature versus mature bone marrow-derived dendritic cells using DNA arrays. Biochem. Biophys. Res. Commun. 2002. 290: 66-72.
27. Ahn, J. H., Lee, Y., Jeon, C., Lee, S. J., Lee, B. H., Choi, K. D. and Bae, Y. S., Identification of the genes differentially expressed in human dendritic cell subsets by cDNA subtraction and microarray analysis. Blood 2002. 100: 1742-1754.
28. Konno, S., Hoshi, T., Taira, T., Plunkett, B. and Huang, S. K., Endotoxin contamination contributes to the in vitro cytokine-inducing activity of osteopontin preparations. J. Interferon Cytokine Res. 2005. 25: 277-282.
29. Shinohara, M. L., Lu, L., Bu, J., Werneck, M. B., Kobayashi, K. S., Glimcher, L. H. and Cantor, H., Osteopontin expression is essential for interferonalpha production by plasmacytoid dendritic cells. Nat. Immunol. 2006. 7: 498-506.
30. Ashkar, S., Weber, G. F., Panoutsakopoulou, V., Sanchirico, M. E., Jansson, M., Zawaideh, S., Rittling, S. R. et al., Eta-1 (osteopontin): an early component of type-1 (cell-mediated) immunity. Science 2000. 287: 860-864.
31. Koguchi, Y., Kawakami, K., Kon, S., Segawa, T., Maeda, M., Uede, T., Saito, A. et al., Penicillium marneffei causes osteopontin-mediated production of interleukin-12 by peripheral blood mononuclear cells. Infect. Immun. 2002. 70: 1042-1048.
32. Renkl, A. C., Wussler, J, Ahrens, T., Thoma, K., Kon, S., Uede, T., Martin, S. F. et al., Osteopontin functionally activates dendritic cells and induces their differentiation towards a Th-1 polarizing phenotype. Blood 2005. 106: 946-955.
33. Abel, B., Freigang, S., Bachmann, M. F., Boschert, U. and Kopf, M., Osteopontin is not required for the development of Th1 responses and viral immunity. J. Immunol. 2005. 175: 6006-6013.
34. Crawford, H. C., Matrisian, L. M. and Liaw, L., Distinct roles of osteopontin in host defense activity and tumor survival during squamous cell carcinoma progression in vivo. Cancer Res. 1998. 58: 5206-5215.
35. Sodek, J., Chen, J., Nagata, T., Kasugai, S., Todescan, R., Jr., Li, I. W. and Kim, R. H., Regulation of osteopontin expression in osteoblasts. Ann. NY Acad. Sci. 1995. 760: 223-241.
36. Shinohara, M. L., Jansson, M., Hwang, E. S., Werneck, M. B. F., Glimcher, L. H. and Cantor, H., T-bet-dependent expression of osteopontin contributes to T-cell polarization. Proc. Natl. Acad. Sci. USA 2005. 102: 17101-17106.
37. Rittling, S. R ., Matsumoto, H. N., McKee, M. D., Nanci, A., An, X. R., Novick, K. E., Kowalski, A. J. et al., Mice lacking osteopontin show normal development and bone structure but display altered osteoclast formation in vitro. J. Bone Miner. Res. 1998. 13: 1101-1111.
38. Kurokawa, M., Kokubu, F., Matsukura, S., Kawaguchi, M., Ieki, K., Suzuki, S., Odaka, M. et al., Effect of corticosteroid on the expression of thymus and activation-regulated chemokine in a murine model of allergic asthma. Int. Arch. Allergy Immunol. 2005. 137: 60-68.
39. Li, X. M., Schofield, B. H., Wang, Q. F., Kim, K. H. and Huang, S. K., Induction of pulmonary allergic responses by antigen-specific Th2 cells. J. Immunol. 1998. 160: 1378-1384.
40. Inaba, K., Inaba, N., Romani, H., Aya, M., Deguchi, S., Ikehara, S., Muramatsu, S. et al., Generation of large numbers of dendritic cells from mouse bone marrow cultures supplemented with granulocyte/macrophage colony-stimulating factor. J. Exp. Med. 1992. 176: 1693-1702.