The cellular niche of listeria monocytogenes infection changes rapidly in the spleen

European Journal of Immunology

Volumn 39, Issue 2, 2009, Pages 417-425

  Aoshi, Taiki ^a   Carrero, Javier A ^a   Konjufca, Vjolica ^a   Koide, Yukio ^b   Unanue, Emil R ^a   Miller, Mark J ^a  

^a WASHINGTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b HAMAMATSU UNIVERSITY SCHOOL OF MEDICINE   (Japan)

Author keywords

Bacterial infection; DC; Listeria monocytogenes; Macrophages; Spleen

Indexed keywords

GLYCOPROTEIN P 15095;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BACTERIAL COLONIZATION; BACTERIAL GROWTH; BACTERIAL VIRULENCE; CELLULAR DISTRIBUTION; CONTROLLED STUDY; DENDRITIC CELL; IMMUNE RESPONSE; IMMUNOHISTOCHEMISTRY; LISTERIA MONOCYTOGENES; LISTERIOSIS; LYMPHOID TISSUE; MOUSE; NONHUMAN; PHAGOCYTE; PRIORITY JOURNAL; SPLEEN; TISSUE SECTION; ANIMAL; BAGG ALBINO MOUSE; IMMUNOLOGY; ISOLATION AND PURIFICATION; MICROBIOLOGY;

ANIMALS; LISTERIA INFECTIONS; LISTERIA MONOCYTOGENES; MICE; MICE, INBRED BALB C; PHAGOCYTES; SPLEEN;

EID: 60749109244     PISSN: 00142980     EISSN: 15214141     Source Type: Journal    
DOI: 10.1002/eji.200838718     Document Type: Article

References (43)

1. Junt, T., Scandella, E. and Ludewig, B., Form follows function: lymphoid tissue microarchitecture in antimicrobial immune defence. Nat. Rev. Immunol. 2008. 8: 764-775.
2. Khanna, K. M. and Lefrançois, L., Geography and plumbing control the T cell response to infection. Immunol. Cell Biol. 2008. 86: 416-422.
3. Kraal, G., Cells in the marginal zone of the spleen. Int. Rev. Cytol. 1992. 132: 31-74.
4. Mebius, R. E. and Kraal, G., Structure and function of the spleen. Nat. Rev. Immunol. 2005. 5: 606-616.
5. Elomaa, O., Kangas, M., Sahlberg, C., Tuukkanen, J., Sormunen, R., Liakka, A., Thesleff, I. et al., Cloning of a novel bacteria-binding receptor structurally related to scavenger receptors and expressed in a subset of macrophages. Cell 1995. 80: 603-609.
6. Sankala, M., Brannstrom, A., Schulthess, T., Bergmann, U., Morgunova, E., Engel, J., Tryggvason, K. and Pikkarainen, T., Characterization of recombinant soluble macrophage scavenger receptor MARCO. J. Biol. Chem. 2002. 277: 33378-33385.
7. Kang, Y. S., Yamazaki, S., Iyoda, T., Pack, M., Bruening, S.A., Kim, J. Y., Takahara, K. et al., SIGN-R1, a novel C-type lectin expressed by marginal zone macrophages in spleen, mediates uptake of the polysaccharide dextran. Int. Immunol. 2003. 15: 177-186.
8. Lanoue, A., Clatworthy, M. R., Smith, P., Green, S., Townsend, M. J., Jolin, H. E., Smith, K. G. et al., SIGN-R1 contributes to protection against lethal pneumococcal infection in mice. J. Exp. Med. 2004. 200: 1383-1393.
9. Kraal, G. and Janse, M., Marginal metallophilic cells of the mouse spleen identified by a monoclonal antibody. Immunology 1986. 58: 665-669.
10. Jones, C., Virji, M. and Crocker, P. R., Recognition of sialylated meningococcal lipopolysaccharide by siglecs expressed on myeloid cells leads to enhanced bacterial uptake. Mol. Microbiol. 2003. 49: 1213-1225.
11. Oetke, C., Kraal, G. and Crocker, P. R., The antigen recognized by MOMA-I is sialoadhesin. Immunol. Lett. 2006. 106: 96-98.
12. Crocker, P. R., Kelm, S., Dubois, C., Martin, B., McWilliam, A. S., Shotton, D. M., Paulson, J. C. and Gordon, S., Purification and properties of sialoadhesin, a sialic acid-binding receptor of murine tissue macrophages. EMBO J. 1991. 10: 1661-1669.
13. Eloranta, M. L. and Alm, G. V., Splenic marginal metallophilic macrophages and marginal zone macrophages are the major interferon-alpha/ beta producers in mice upon intravenous challenge with herpes simplex virus. Scand. J. Immunol. 1999. 49: 391-394.
14. Jablonska, J., Dittmar, K. E., Kleinke, T., Buer, J. and Weiss, S., Essential role of CCL2 in clustering of splenic ERTR-9+macrophages during infection of BALB/c mice by Listeria monocytogenes. Infect. Immun. 2007. 75: 462-470.
15. Nathan, C., Neutrophils and immunity: Challenges and opportunities. Nat. Rev. Immunol. 2006. 6: 173-182.
16. Conlan, J. W. and North, R. J., Neutrophils are essential for early anti-Listeria defense in the liver, but not in the spleen or peritoneal cavity, as revealed by a granulocyte-depleting monoclonal antibody. J. Exp. Med. 1994. 179: 259-268.
17. Czuprynski, C. J., Brown, J. F., Maroushek, N., Wagner, R. D. and Steinberg, H., Administration of anti-granulocyte mAb RB6-8C5 impairs the resistance of mice to Listeria monocytogenes infection. J. Immunol. 1994. 152: 1836-1846.
18. Rogers, H. W. and Unanue, E. R., Neutrophils are involved in acute, nonspecific resistance to Listeria monocytogenes in mice. Infect. Immun. 1993. 61: 5090-5096.
19. Unanue, E. R., Inter-relationship among macrophages, natural killer cells and neutrophils in early stages of Listeria resistance. Curr. Opin. Immunol. 1997. 9: 35-43.
20. Witmer, M. D. and Steinman, R. M., The anatomy of peripheral lymphoid organs with emphasis on accessory cells: Light-microscopic immunocytochemical studies of mouse spleen, lymph node, and Peyer's patch. Am. J. Anat. 1984. 170: 465-481.
21. Dudziak, D., Kamphorst, A. O., Heidkamp, G. F., Buchholz, V. R., Trumpfheller, C., Yamuzaki, S., Cheong, C. et al., Differential antigen processing by dendritic cell subsets in vivo. Science 2007. 315: 107-111.
22. Austyn, J. M. and Gordon, S., F4/80, a monoclonal antibody directed specifically against the mouse macrophage. Eur. J. Immunol. 1981. 11: 805-815.
23. Oldenborg, P. A., Zheleznyak, A., Fang, Y. F., Lagenaur, C. F., Gresham, H. D. and Lindberg, F. P., Role of CD47 as a marker of self on red blood cells. Science 2000. 288: 2051-2054.
24. Pamer, E. G., Immune responses to Listeria monocytogenes. Nat. Rev. Immunol. 2004. 4: 812-823.
25. Aichele, P., Zinke, J., Grode, L., Schwendener, R. A., Kaufmann, S. H. and Seiler, P., Macrophages of the splenic marginal zone are essential for trapping of blood-borne particulate antigen but dispensable for induction of specific T cell responses. J. Immunol. 2003. 171: 1148-1155.
26. Conlan, J. W., Early pathogenesis of Listeria monocytogenes infection in the mouse spleen. J. Med. Microbiol. 1996. 44: 295-302.
27. Muraille, E., Giannino, R., Guirnalda, P., Leiner, I., Jung, S., Parner, E. G. and Lauvau, G., Distinct in vivo dendritic cell activation by live versus killed Listeria monocytogenes. Eur. J. Immunol. 2005. 35: 1463-1471.
28. Neuenhahn, M., Kerksiek, K. M., Nauerth, M., Suhre, M. H., Schiemann, M., Gebhardt, F. E., Sternberger, C. et al., CD8alpha+dendritic cells: Are required for efficient entry of Listeria monocytogenes into the spleen. Immunity 2006. 25: 619-630.
29. Dijkstra, C. D., Van Vliet, E., Dopp, E. A., van der Lelij, A. A. and Kraal, G., Marginal zone macrophages identified by a monoclonal antibody: Characterization of immuno- and enzyme-histochemical properties and functional capacities. Immunology 1985. 55: 23-30.
30. Metlay, J. P., Witmer-Pack, M. D., Agger, R., Crowley, M. T., Lawless, D. and Steinman, R. M., The distinct leukocyte integrins of mouse spleen dendritic cells as identified with new hamster monoclonal antibodies. J. Exp. Med. 1990. 171: 1753-1771.
31. Mitchell, J., Lymphocyte circulation in the spleen. Marginal zone bridging channels and their possible role in cell traffic. Immunology 1973. 24: 93-107.
32. Steinman, R. M., Pack, M. and Inaba, K., Dendritic cells in the T-cell areas of lymphoid organs. Immunol. Rev. 1997. 156: 25-37.
33. Manders, E. M. M., Verbeek, F. J. and Aten, J. A., Measurement of colocalization of objects in dual-color confocal images. J. Microsc.-Oxford 1993. 169: 375-382.
34. O'Riordan, M., Moors, M. A. and Portnoy, D. A., Listeria intracellular growth and virulence require host-derived lipoic acid. Science 2003. 302: 462-464.
35. Aoshi, T., Zinselmeyer, B. H., Konjufca, V., Lynch, J. N., Zhang, X., Koide, Y. and Miller, M. J., Bacterial entry to the splenic white pulp initiates antigen presentation to CD8+T cells. Immunity 2008. 29: 476-486.
36. Taylor, P. R., Martinez-Pomares, L., Stacey, M., Lin, H. H., Brown, G. D. and Gordon, S., Macrophage receptors and immune recognition. Annu. Rev. Immunol. 2005. 23: 901-944.
37. Nussenzweig, M. C., Steinman, R. M., Witmer, M. D. and Gutchinov, B., A monoclonal antibody specific for mouse dendritic cells. Proc. Natl. Acad. Sci. USA 1982. 79: 161-165.
38. Serbina, N. V., Salazar-Mather, T. P., Biron, C. A., Kuziel, W. A. and Pamer, E. G., TNF/iNOS-producing dendritic cells mediate innate immune defense against bacterial infection. Immunity 2003. 19: 59-70.
39. Tam, M. A. and Wick, M. J., Differential expansion, activation and effector functions of conventional and plasmacytoid dendritic cells in mouse tissues transiently infected with Listeria monocytogenes. Cell. Microbiol. 2006. 8: 1172-1187.
40. Arredouani, M., Yang, Z., Ning, Y., Qin, G., Soininen, R., Tryggvason, K. and Kobzik, L., The scavenger receptor MARCO is required for lung defense against pneumococcal pneumonia and inhaled particles. J. Exp. Med. 2004. 200: 267-272.
41. Odermatt, B., Eppler, M., Leist, T. P., Hengartner, H. and Zinkernagel, R. M., Virus-triggered acquired immunodeficiency by cytotoxic T-cell-dependent destruction of antigen-presenting cells and lymph follicle structure. Proc. Natl. Acad. Sci. USA 1991. 88: 8252-8256.
42. Seiler, P., Aichele, P., Odermatt, B., Hengartner, H., Zinkernagel, R. M. and Schwendener, R. A., Crucial role of marginal zone macrophages and marginal zone metallophils in the clearance of lymphocytic choriomeningitis virus infection. Eur. J. Immunol. 1997. 27: 2626-2633.
43. Carrero, J. A., Calderon, B. and Unanue, E. R., Lymphocytes are detrimental during the early innate immune response against Listeria monocytogenes. J. Exp. Med. 2006. 203: 933-940.