Murine spleen contains a diversity of myeloid and dendritic cells distinct in antigen presenting function

Journal of Cellular and Molecular Medicine

Volumn 16, Issue 11, 2012, Pages 2611-2619

  Hey, Ying Y ^a   O'Neill, Helen C ^a  

^a AUSTRALIAN NATIONAL UNIVERSITY   (Australia)

Author keywords

Antigen presentation; Dendritic cell; Myeloid cell

Indexed keywords

ANIMAL; ANTIGEN PRESENTATION; ANTIGEN PRESENTING CELL; ARTICLE; BONE MARROW CELL; CULTURE TECHNIQUE; CYTOLOGY; DENDRITIC CELL; HUMAN; IMMUNOLOGY; MACROPHAGE; METHODOLOGY; MONOCYTE; SPLEEN;

ANIMALS; ANTIGEN PRESENTATION; ANTIGEN-PRESENTING CELLS; CELL CULTURE TECHNIQUES; DENDRITIC CELLS; HUMANS; MACROPHAGES; MONOCYTES; MYELOID CELLS; SPLEEN;

MURINAE;

EID: 84868121639     PISSN: 15821838     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1582-4934.2012.01608.x     Document Type: Article

References (84)

1. Adema GJ. Dendritic cells from bench to bedside and back. Immunol Lett. 2009; 122: 135-7.
2. Cesta MF. Normal structure, function, and histology of the spleen. Toxicol Pathol. 2006; 34: 455-65.
3. Mebius RE, Kraal G. Structure and function of the spleen. Nat Rev Immunol. 2005; 5: 606-16.
4. Heath WR, Belz GT, Behrens GMN, et al. Cross-presentation, dendritic cell subsets, and the generation of immunity to cellular antigens. Immunol Rev. 2004; 199: 9-26.
5. Naik SH. Demystifying the development of dendritic cell subtypes, a little. Immunol Cell Biol. 2008; 86: 439-52.
6. Shortman K, Naik SH. Steady-state and inflammatory dendritic-cell development. Nat Rev. 2007; 7: 19-30.
7. Steinman RM, Cohn ZA. Identification of a novel cell type in peripheral lymphoid organs of mice. I. Morphology, quantitation, tissue distribution. J Exp Med. 1973; 137: 1142-62.
8. Nussenzweig MC, Steinman RM, Witmer MD, et al. A monoclonal antibody specific for mouse dendritic cells. Proc Natl Acad Sci USA. 1982; 79: 161-5.
9. Vremec D, Pooley J, Hochrein H, et al. CD4 and CD8 expression by dendritic cell subtypes in mouse thymus and spleen. J Immunol. 2000; 164: 2978-86.
10. Hochrein H, Shortman K, Vremec D, et al. Differential production of IL-12, IFN-α, and IFN-β by mouse dendritic cell subsets. J Immunol. 2001; 166: 5448-55.
11. De Smedt T, Pajak B, Muraille E, et al. Regulation of dendritic cell numbers and maturation by lipopolysaccharide in vivo. J Exp Med. 1996; 184: 1413-24.
12. Steinman RM, Pack M, Inaba K. Dendritic cells in the T-cell areas of lymphoid organs. Immunol Rev. 1997; 156: 25-37.
13. Lauterbach H, Bathke B, Gilles S, et al. Mouse CD8alpha+ DCs and human BDCA3+ DCs are major producers of IFN-lambda in response to poly IC. J Exp Med. 2010; 207: 2703-17.
14. Isaacs A, Lindenmann J. Virus interference. 1. The interferon. Proc R Soc Biol. 1957; 147: 258-67.
15. Fitzgerald-Bocarsly P, Dai J, Singh S. Plasmacytoid dendritic cells and type I IFN: 50 years of convergent history. Cytokine Growth Factor Rev. 2008; 19: 3-19.
16. Ronnblom L, Ramstedt U, Alm GV. Properties of human natural interferon-producing cells stimulated by tumor cell lines. Eur J Immunol. 1983; 13: 471-6.
17. Facchetti F, De Wolf-Peeters C, Mason DY, et al. Plasmacytoid T cells Immunohistochemical evidence for their monocyte/macrophage origin. Am J Path. 1988; 133: 15-21.
18. Cella M, Jarrossay D, Faccheth F, et al. Plasmacytoid monocytes migrate to inflamed lymph nodes and produce large amounts of type I interferon. Nat Med. 1999; 5: 919-23.
19. Grouard G, Rissoan MC, Filgueira L, et al. The enigmatic plasmacytoid T cells develop into dendritic cells with interleukin (IL)-3 and CD40-ligand. J Exp Med. 1997; 185: 1101-11.
20. Siegal FP, Kadowaki N, Shodell M, et al. The nature of the principal Type 1 interferon-producing cells in human blood. Science. 1999; 284: 1835-7.
21. Pelayo R, Hirose J, Huang J, et al. Derivation of 2 categories of plasmacytoid dendritic cells in murine bone marrow. Blood. 2005; 105: 4407-15.
22. Onai N, Obata-Onai A, Schmid MA, et al. Identification of clonogenic common Flt3+M-CSFR+ plasmacytoid and conventional dendritic cell progenitors in mouse bone marrow. Nat Immunol. 2007; 8: 1207-16.
23. O'Keeffe M, Hochrein H, Vremec D, et al. Mouse plasmacytoid cells: long-lived cells, heterogeneous in surface phenotype and function, that differentiate into CD8- dendritic cells only after microbial stimulus. J Exp Med. 2002; 196: 1307-19.
24. Diebold SS, Montoya M, Unger H, et al. Viral infection switches non-plasmacytoid dendritic cells into high interferon producers. Nature. 2003; 424: 324-8.
25. Inaba K, Steinman RM, Pack MW, et al. Identification of proliferating dendritic cell precursors in mouse blood. J Exp Med. 1992; 175: 1157-67.
26. Randolph GJ, Inaba K, Robbiani DF, et al. Differentiation of phagocytic monocytes into lymph node dendritic cells in vivo. Immunity. 1999; 11: 753-61.
27. Randolph GJ, Beaulieu S, Lebecque S, et al. Differentiation of monocytes into dendritic cells in a model of transendothelial trafficking. Science. 1998; 282: 480-3.
28. Cheong C, Matos I, Choi JH, et al. Microbial stimulation fully differentiates monocytes to DC-SIGN/CD209+ dendritic cells for immune T cell areas. Cell. 2010; 143: 416-29.
29. von Euw EM, Barrio MM, Furman D, et al. Monocyte-derived dendritic cells loaded with a mixture of apoptotic/necrotic melanoma cells efficiently cross-present gp100 and MART-1 antigens to specific CD8+ T lymphocytes. J Transl Med. 2007; 5. doi:10.1186/1479-5876-5-19.
30. Geissmann F, Auffray C, Palframan R, et al. Blood monocytes: distinct subsets, how they relate to dendritic cells, and their possible roles in the regulation of T-cell responses. Immunol Cell Biol. 2008; 86: 398-408.
31. Leon B, Lopez-Bravo M, Ardavin C. Monocytes-derived dendritic cells formed at the infection site control the induction of protective T helper 1 responses against Leishmania. Immunity. 2007; 26: 519-31.
32. Serbina NV, Salazar-Mather TP, Biron CA, et al. TNF/iNOS-producing dendritic cells mediate innate immune defense against bacterial infection. Immunity. 2003; 19: 59-70.
33. Steinbrink K, Wolfl M, Jonuleit H, et al. Induction of Tolerance by IL-10-Treated Dendritic Cells. J Immunol. 1997; 159: 4772-80.
34. Wakkach A, Fournier N, Brun V, et al. Characterization of dendritic cells that induce tolerance and T regulatory 1 cell differentiation in vivo. Immunity. 2003; 18: 605-17.
35. Tang H, Guo Z, Zhang M, et al. Endothelial stroma programs hematopoietic stem cells to differentiate into regulatory dendritic cells through IL-10. Blood. 2006; 108: 1189-97.
36. Zhang M, Tang H, Guo Z, et al. Splenic stroma drives mature dendritic cells to differentiate into regulatory dendritic cells. Nat Immunol. 2004; 5: 1124-33.
37. Liu K, Victora GD, Schwickert TA, et al. In vivo analysis of dendritic cell development and homeostasis. Science. 2009; 324: 392-7.
38. Diao J, Winter E, Cantin C, et al. In situ replication of immediate dendritic cell (DC) precursors contributes to conventional DC homeostasis in lymphoid tissue. J Immunol. 2006; 176: 7196-206.
39. Geissmann F, Jung S, Littman DR. Blood monocytes consist of two principal subsets with distinct migratory properties. Immunity. 2003; 19: 71-82.
40. Swirski FK, Nahrendorf M, Etzrodt M, et al. Identification of splenic reservoir monocytes and their deployment to inflammatory sites. Science. 2009; 325: 612-6.
41. Kang YS, Yamazaki S, Iyoda T, 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: 177-86.
42. Oehen S, Odermatt B, Karrer U, et al. Marginal zone macrophages and immune responses against viruses. J Immunol. 2002; 169: 1453-8.
43. Elomaa O, Kangas M, Sahlberg C, et al. Cloning of a novel bacteria-binding receptor structurally related to scavenger receptors and expressed in a subset of macrophages. Cell. 1995; 80: 603-9.
44. Noel G, Guo X, Wang Q, et al. Postburn monocytes are the major producers of TNF-alpha in the heterogeneous splenic macrophage population. Shock. 2007; 27: 312-9.
45. Diao J, Winter E, Chen W, et al. Characterization of distinct conventional and plasmacytoid dendritic cell-committed precursors in murine bone marrow. J Immunol. 2004; 173: 1826-33.
46. Saunders D, Lucas K, Ismaili J, et al. Dendritic cell development in culture from thymic precursor cells in the absence of granulocyte/macrophage colony-stimulating factor. J Exp Med. 1996; 184: 2185-96.
47. Varol C, Landsman L, Fogg DK, et al. Monocytes give rise to mucosal, but not splenic, conventional dendritic cells. J Exp Med. 2007; 204: 171-80.
48. Fogg DK, Sibon C, Miled C, et al. A clonogenic bone harrow progenitor specific for macrophages and dendritic cells. Science. 2006; 311: 83-7.
49. Naik SH, Metcalf D, van Nieuwenhuijze A, et al. Intrasplenic steady-state dendritic cell precursors that are distinct from monocytes. Nat Immunol. 2006; 7: 663-71.
50. Groothuis TA, Neefjes J. The many roads to cross-presentation. J Exp Med. 2005; 202: 1313-8.
51. Sigal LJ, Crotty S, Andino R, et al. Cytotoxic T-cell immunity to virus-infected non-haematopoietic cells requires presentation of exogenous antigen. Nature. 1999; 398: 77-80.
52. Huang AYC, Bruce AT, Pardoll DM, et al. In vivo cross-priming of MHC class I-restricted antigens requires the TAP transporter. Immunity. 1996; 4: 349-55.
53. Den Haan JMM, Lehar SM, Bevan MJ. CD8+ but not CD8- dendritic cells cross-prime cytotoxic T cells in vivo. J Exp Med. 2000; 192: 1685-95.
54. Dudziak D, Kamphorst AO, Heidkamp GF, et al. Differential antigen processing by dendritic cell subsets in vivo. Science. 2007; 315: 107-11.
55. Pooley JL, Heath WR, Shortman K. Cutting edge: intravenous soluble antigen is presented to CD4 T cells by CD8- dendritic cells, but cross-presented to CD8 T cells by CD8+ dendritic cells. J Immunol. 2001; 166: 5327-30.
56. Schulz O, Reis E, Sousa C. Cross-presentation of cell-associated antigens by CD8+ dendritic cells is attributable to their ability to internalize dead cells. Immunology. 2002; 107: 183-9.
57. Gagnon E, Duclos S, Rondeau C, et al. Endoplasmic reticulum-mediated phagocytosis is a mechanism of entry into macrophages. Cell. 2002; 110: 119-31.
58. Vyas JM, Van der Veen AG, Ploegh HL. The known unknowns of antigen processing and presentation. Nat Rev Immunol. 2008; 8: 607-18.
59. Beauvillain C, Delneste Y, Scotet M, et al. Neutrophils efficiently cross-prime naive T cells in vivo. Blood. 2007; 110: 2965-73.
60. Ramirez MC, Sigal LJ. Macrophages and dendritic cells use the cytosolic pathway to rapidly cross-present antigen from live, vaccinia-infected cells. J Immunol. 2002; 169: 6733-42.
61. Randolph GJ, Jakubzick C, Qu C. Antigen presentation by monocytes and monocyte-derived cells. Curr Opin Immunol. 2008; 20: 52-60.
62. Xu Y, Zhan Y, Lew AM, et al. Differential Development of murine dendritic cells by GM-CSF versus Flt3 ligand has implications for inflammation and trafficking. J Immunol. 2007; 179: 7577-84.
63. Sallusto F, Lanzavecchia A. Efficient presentation of soluble antigen by cultured human dendritic cells is maintained by granulocyte/macrophage colony-stimulating factor plus interleukin 4 and downregulated by tumor necrosis factor α. J Exp Med. 1994; 179: 1109-18.
64. Brawand P, Fitzpatrick DR, Greenfield BW, et al. Murine plasmacytoid pre-dendritic cells generated from Flt3 ligand-supplemented bone marrow cultures are immature APCs. J Immunol. 2002; 169: 6711-9.
65. Naik SH, Proietto AI, Wilson NS, et al. Cutting Edge: generation of Splenic CD8+ and CD8- Dendritic Cell Equivalents in Fms-Like Tyrosine Kinase 3 Ligand Bone Marrow Cultures. J Immunol. 2005; 174: 6592-7.
66. Roy KC, Bandyopadhyay G, Rakshit S, et al. IL-4 alone without the involvement of GM-CSF transforms human peripheral blood monocytes to aCD1adim, CD83+ myeloid dendritic cell subset. J Cell Sci. 2004; 117: 3435-45.
67. Vremec D, Lieschke GJ, Dunn AR, et al. The influence of granulocyte/macrophage colony-stimulating factor on dendritic cell levels in mouse lymphoid organs. Eur J Immunol. 1997; 27: 40-4.
68. Tan JKH, O'Neill HC. Haematopoietic stem cells in spleen have distinct differentiative potential for antigen presenting cells. J Cell Mol Med. 2010; 14: 2144-50.
69. Brasel K, De Smedt T, Smith JL, et al. Generation of murine dendritic cells from flt3-ligand-supplemented bone marrow cultures. Blood. 2000; 96: 3029-39.
70. Merad M, Manz MG. Dendritic cell homeostasis. Blood. 2009; 113: 3418-27.
71. McKenna HJ, Stocking KL, Miller RE, et al. Mice lacking flt3 ligand have deficient hematopoiesis affecting hematopoietic progenitor cells, dendritic cells, and natural killer cells. Blood. 2000; 95: 3489-97.
72. Sunderkötter C, Nikolic T, Dillon MJ, et al. Subpopulations of mouse blood monocytes differ in maturation stage and inflammatory response. J Immunol. 2004; 172: 4410-7.
73. O'Neill HC, Wilson HL, Quah B, et al. Dendritic cell development in long-term spleen stromal cultures. Stem Cells. 2004; 22: 475-86.
74. Wilson HL, Ni K, O'Neill HC. Identification of progenitor cells in long-term spleen stromal cultures that produce immature dendritic cells. Proc Natl Acad Sci USA. 2000; 97: 4784-9.
75. Wilson H, O'Neill HC. Dynamics of dendritic cell development from precursors maintained in stroma-dependent long-term cultures. Immunol Cell Biol. 2004; 81: 144-51.
76. Despars G, O'Neill HC. Splenic endothelial cells support development of dendritic cells from bone marrow. Stem Cells. 2006; 24: 1496-504.
77. Quah B, Ni K, O'Neill HC. In vitro hematopoiesis produces a distinct class of immature dendritic cells from spleen progenitors with limited T cell stimulation capacity. Int Immunol. 2004; 16: 567-77.
78. Iyoda T, Shimoyama S, Liu K, et al. The CD8+ dendritic cell subset selectively endocytoses dying cells in culture and in vivo. J Exp Med. 2002; 195: 1289-302.
79. Morelli AE, Larregina AT, Shufesky WJ, et al. Internalization of circulating apoptotic cells by splenic marginal zone dendritic cells: dependence on complement receptors and effect on cytokine production. Blood. 2003; 101: 611-20.
80. Belz GT, Smith CM, Kleinert L, et al. Distinct migrating and nonmigrating dendritic cell populations are involved in MHC class I-restricted antigen presentation after lung infection with virus. Proc Natl Acad Sci USA. 2004; 101: 8670-5.
81. Nolte MA, T Hoen ENM, Van Stijn A, et al. Isolation of the intact white pulp. Quantitative and qualitative analysis of the cellular composition of the splenic compartments. Eur J Immunol. 2000; 30: 626-34.
82. Abadie V, Badell E, Douillard P, et al. Neutrophils rapidly migrate via lymphatics after Mycobacterium bovis BCG intradermal vaccination and shuttle live bacilli to the draining lymph nodes. Blood. 2005; 106: 1843-50.
83. Tvinnereim AR, Hamilton SE, Harty JT. Neutrophil involvement in cross-priming CD8+ T cell responses to bacterial antigens. J Immunol. 2004; 173: 1994-2002.
84. Witmer-Pack MD, Hughes DA, Schuler G, et al. Identification of macrophages and dendritic cells in the osteopetrotic (op/op) mouse. J Cell Sci. 1993; 104: 1021-9.