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Langerhans cells arise from monocytes in vivo

Abstract

Langerhans cells (LCs) are the only dendritic cells of the epidermis and constitute the first immunological barrier against pathogens and environmental insults. The factors regulating LC homeostasis remain elusive and the direct circulating LC precursor has not yet been identified in vivo. Here we report an absence of LCs in mice deficient in the receptor for colony-stimulating factor 1 (CSF-1) in steady-state conditions. Using bone marrow chimeric mice, we have established that CSF-1 receptor–deficient hematopoietic precursors failed to reconstitute the LC pool in inflamed skin. Furthermore, monocytes with high expression of the monocyte marker Gr-1 (also called Ly-6c/G) were specifically recruited to the inflamed skin, proliferated locally and differentiated into LCs. These results identify Gr-1hi monocytes as the direct precursors for LCs in vivo and establish the importance of the CSF-1 receptor in this process.

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Figure 1: LC development in CSF-1- and CSF-1R-deficient mice.
Figure 2: Function of CSF-1R in LC differentiation in vivo.
Figure 3: Gr-1hi monocytes infiltrate and proliferate in situ in ultraviolet irradiation–inflamed skin.
Figure 4: Bead-positive Gr-1hi monocytes differentiate into dermal macrophages and epidermal LCs in inflamed skin.
Figure 5: Skin-infiltrating Gr-1hi monocytes differentiate into LCs.
Figure 6: Adoptive transfer of Gr-1hi monocytes in vivo.

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References

  1. Hemmi, H. et al. Skin antigens in the steady state are trafficked to regional lymph nodes by transforming growth factor-β1-dependent cells. Int. Immunol. 13, 695–704 (2001).

    Article  CAS  Google Scholar 

  2. Kripke, M.L., Munn, C.G., Jeevan, A., Tang, J.M. & Bucana, C. Evidence that cutaneous antigen-presenting cells migrate to regional lymph nodes during contact sensitization. J. Immunol. 145, 2833–2838 (1990).

    CAS  PubMed  Google Scholar 

  3. Schuler, G. & Steinman, R.M. Murine epidermal Langerhans cells mature into potent immunostimulatory dendritic cells in vitro. J. Exp. Med. 161, 526–546 (1985).

    Article  CAS  Google Scholar 

  4. Tang, H.L. & Cyster, J.G. Chemokine up-regulation and activated T cell attraction by maturing dendritic cells. Science 284, 819–822 (1999).

    Article  CAS  Google Scholar 

  5. Mayerova, D., Parke, E.A., Bursch, L.S., Odumade, O.A. & Hogquist, K.A. Langerhans cells activate naive self-antigen-specific CD8 T cells in the steady state. Immunity 21, 391–400 (2004).

    Article  CAS  Google Scholar 

  6. Allan, R.S. et al. Epidermal viral immunity induced by CD8α+ dendritic cells but not by Langerhans cells. Science 301, 1925–1928 (2003).

    Article  CAS  Google Scholar 

  7. Kissenpfennig, A. et al. Dynamics and function of Langerhans cells in vivo: dermal dendritic cells colonize lymph node areas distinct from slower migrating Langerhans cells. Immunity 22, 643–654 (2005).

    Article  CAS  Google Scholar 

  8. Bennett, C.L. et al. Inducible ablation of mouse Langerhans cells diminishes but fails to abrogate contact hypersensitivity. J. Cell Biol. 169, 569–576 (2005).

    Article  CAS  Google Scholar 

  9. Merad, M. et al. Langerhans cells renew in the skin throughout life under steady-state conditions. Nat. Immunol. 3, 1135–1141 (2002).

    Article  CAS  Google Scholar 

  10. Witmer-Pack, M.D. et al. Identification of macrophages and dendritic cells in the osteopetrotic (op/op) mouse. J. Cell Sci. 104, 1021–1029 (1993).

    PubMed  Google Scholar 

  11. Takahashi, K., Naito, M. & Shultz, L.D. Differentiation of epidermal Langerhans cells in macrophage colony-stimulating-factor-deficient mice homozygous for the osteopetrosis (op) mutation. J. Invest. Dermatol. 99, 46S–47S (1992).

    Article  CAS  Google Scholar 

  12. Wiktor-Jedrzejczak, W.W., Ahmed, A., Szczylik, C. & Skelly, R.R. Hematological characterization of congenital osteopetrosis in op/op mouse. Possible mechanism for abnormal macrophage differentiation. J. Exp. Med. 156, 1516–1527 (1982).

    Article  CAS  Google Scholar 

  13. Wiktor-Jedrzejczak, W. & Gordon, S. Cytokine regulation of the macrophage (MΦ) system studied using the colony stimulating factor-1-deficient op/op mouse. Physiol. Rev. 76, 927–947 (1996).

    Article  CAS  Google Scholar 

  14. del Hoyo, G.M. et al. Characterization of a common precursor population for dendritic cells. Nature 415, 1043–1047 (2002).

    Article  Google Scholar 

  15. Caux, C. et al. CD34+ hematopoietic progenitors from human cord blood differentiate along two independent dendritic cell pathways in response to GM-CSF+TNF-α. J. Exp. Med. 184, 695–706 (1996).

    Article  CAS  Google Scholar 

  16. Ito, T. et al. A CD1a+/CD11c+ subset of human blood dendritic cells is a direct precursor of Langerhans cells. J. Immunol. 163, 1409–1419 (1999).

    CAS  PubMed  Google Scholar 

  17. Geissmann, F. et al. Transforming growth factor β1, in the presence of granulocyte/macrophage colony-stimulating factor and interleukin 4, induces differentiation of human peripheral blood monocytes into dendritic Langerhans cells. J. Exp. Med. 187, 961–966 (1998).

    Article  CAS  Google Scholar 

  18. Larregina, A.T. et al. Dermal-resident CD14+ cells differentiate into Langerhans cells. Nat. Immunol. 2, 1151–1158 (2001).

    Article  CAS  Google Scholar 

  19. Borkowski, T.A., Letterio, J.J., Farr, A.G. & Udey, M.C. A role for endogenous transforming growth factor β1 in Langerhans cell biology: the skin of transforming growth factor β1 null mice is devoid of epidermal Langerhans cells. J. Exp. Med. 184, 2417–2422 (1996).

    Article  CAS  Google Scholar 

  20. Dai, X.M. et al. Targeted disruption of the mouse colony-stimulating factor 1 receptor gene results in osteopetrosis, mononuclear phagocyte deficiency, increased primitive progenitor cell frequencies, and reproductive defects. Blood 99, 111–120 (2002).

    Article  CAS  Google Scholar 

  21. Cecchini, M.G. et al. Role of colony stimulating factor-1 in the establishment and regulation of tissue macrophages during postnatal development of the mouse. Development 120, 1357–1372 (1994).

    CAS  PubMed  Google Scholar 

  22. Pixley, F.J. & Stanley, E.R. CSF-1 regulation of the wandering macrophage: complexity in action. Trends Cell Biol. 14, 628–638 (2004).

    Article  CAS  Google Scholar 

  23. Byrne, P.V., Guilbert, L.J. & Stanley, E.R. Distribution of cells bearing receptors for a colony-stimulating factor (CSF-1) in murine tissues. J. Cell Biol. 91, 848–853 (1981).

    Article  CAS  Google Scholar 

  24. Qu, C. et al. Role of CCR8 and other chemokine pathways in the migration of monocyte-derived dendritic cells to lymph nodes. J. Exp. Med. 200, 1231–1241 (2004).

    Article  CAS  Google Scholar 

  25. Sunderkotter, C. et al. Subpopulations of mouse blood monocytes differ in maturation stage and inflammatory response. J. Immunol. 172, 4410–4417 (2004).

    Article  Google Scholar 

  26. Dai, X.M., Zong, X.H., Akhter, M.P. & Stanley, E.R. Osteoclast deficiency results in disorganized matrix, reduced mineralization, and abnormal osteoblast behavior in developing bone. J. Bone Miner. Res. 19, 1441–1451 (2004).

    Article  CAS  Google Scholar 

  27. Geissmann, F., Jung, S. & Littman, D.R. Blood monocytes consist of two principal subsets with distinct migratory properties. Immunity 19, 71–82 (2003).

    Article  CAS  Google Scholar 

  28. Passlick, B., Flieger, D. & Ziegler-Heitbrock, H.W. Identification and characterization of a novel monocyte subpopulation in human peripheral blood. Blood 74, 2527–2534 (1989).

    CAS  PubMed  Google Scholar 

  29. Randolph, G.J., Sanchez-Schmitz, G., Liebman, R.M. & Schakel, K. The CD16+ (FcγRIII+) subset of human monocytes preferentially becomes migratory dendritic cells in a model tissue setting. J. Exp. Med. 196, 517–527 (2002).

    Article  CAS  Google Scholar 

  30. Tacke, F. et al. Immature monocytes acquire antigens from other cells in the bone marrow and present them to T cells after maturing in the periphery. (in the press).

  31. Merad, M. et al. Depletion of host Langerhans cells before transplantation of donor alloreactive T cells prevents skin graft-versus-host disease. Nat. Med. 10, 510–517 (2004).

    Article  CAS  Google Scholar 

  32. Bruno, L., Seidl, T. & Lanzavecchia, A. Mouse pre-immunocytes as non-proliferating multipotent precursors of macrophages, interferon-producing cells, CD8α+ and CD8α− dendritic cells. Eur. J. Immunol. 31, 3403–3412 (2001).

    Article  CAS  Google Scholar 

  33. Schaerli, P., Willimann, K., Ebert, L.M., Walz, A. & Moser, B. Cutaneous CXCL14 targets blood precursors to epidermal niches for Langerhans cell differentiation. Immunity 23, 331–342 (2005).

    Article  CAS  Google Scholar 

  34. Ryan, G.R. et al. Rescue of the colony-stimulating factor 1 (CSF-1)-nullizygous mouse (Csf1op/Csf1op) phenotype with a CSF-1 transgene and identification of sites of local CSF-1 synthesis. Blood 98, 74–84 (2001).

    Article  CAS  Google Scholar 

  35. Roth, P. & Stanley, E.R. The biology of CSF-1 and its receptor. Curr. Top. Microbiol. Immunol. 181, 141–167 (1992).

    CAS  PubMed  Google Scholar 

  36. Hume, D.A. & Favot, P. Is the osteopetrotic (op/op mutant) mouse completely deficient in expression of macrophage colony-stimulating factor? J. Interferon Cytokine Res. 15, 279–284 (1995).

    Article  CAS  Google Scholar 

  37. Mende, I., Karsunky, H., Weissman, I.L., Engleman, E.G. & Merad, M. Flk2+ myeloid progenitors are the main source of Langerhans cells. Blood (2005).

  38. Hannum, C. et al. Ligand for FLT3/FLK2 receptor tyrosine kinase regulates growth of haematopoietic stem cells and is encoded by variant RNAs. Nature 368, 643–648 (1994).

    Article  CAS  Google Scholar 

  39. Hume, D.A., Pavli, P., Donahue, R.E. & Fidler, I.J. The effect of human recombinant macrophage colony-stimulating factor (CSF-1) on the murine mononuclear phagocyte system in vivo. J. Immunol. 141, 3405–3409 (1988).

    CAS  PubMed  Google Scholar 

  40. Tushinski, R.J. et al. Survival of mononuclear phagocytes depends on a lineage-specific growth factor that the differentiated cells selectively destroy. Cell 28, 71–81 (1982).

    Article  CAS  Google Scholar 

  41. Metcalf, D. The granulocyte-macrophage colony-stimulating factors. Science 229, 16–22 (1985).

    Article  CAS  Google Scholar 

  42. Korn, A.P., Henkelman, R.M., Ottensmeyer, F.P. & Till, J.E. Investigations of a stochastic model of haemopoiesis. Exp. Hematol. 1, 362–375 (1973).

    CAS  PubMed  Google Scholar 

  43. Nakahata, T., Gross, A.J. & Ogawa, M. A stochastic model of self-renewal and commitment to differentiation of the primitive hemopoietic stem cells in culture. J. Cell. Physiol. 113, 455–458 (1982).

    Article  CAS  Google Scholar 

  44. Lagasse, E. & Weissman, I.L. Enforced expression of Bcl-2 in monocytes rescues macrophages and partially reverses osteopetrosis in op/op mice. Cell 89, 1021–1031 (1997).

    Article  CAS  Google Scholar 

  45. Romani, N., Schuler, G. & Fritsch, P. Ontogeny of Ia-positive and Thy-1-positive leukocytes of murine epidermis. J. Invest. Dermatol. 86, 129–133 (1986).

    Article  CAS  Google Scholar 

  46. Elbe, A. et al. Maturational steps of bone marrow-derived dendritic murine epidermal cells. Phenotypic and functional studies on Langerhans cells and Thy-1+ dendritic epidermal cells in the perinatal period. J. Immunol. 143, 2431–2438 (1989).

    CAS  PubMed  Google Scholar 

  47. Tripp, C.H. et al. Ontogeny of Langerin/CD207 expression in the epidermis of mice. J. Invest. Dermatol. 122, 670–672 (2004).

    Article  CAS  Google Scholar 

  48. Beverley, P.C., Egeler, R.M., Arceci, R.J. & Pritchard, J. The Nikolas Symposia and histiocytosis. Nat. Rev. Cancer 5, 488–494 (2005).

    Article  CAS  Google Scholar 

  49. Rolland, A. et al. Increased blood myeloid dendritic cells and dendritic cell-poietins in Langerhans cell histiocytosis. J. Immunol. 174, 3067–3071 (2005).

    Article  CAS  Google Scholar 

  50. Banchereau, J. et al. Immune and clinical responses in patients with metastatic melanoma to CD34+ progenitor-derived dendritic cell vaccine. Cancer Res. 61, 6451–6458 (2001).

    CAS  PubMed  Google Scholar 

  51. Boring, L. et al. Impaired monocyte migration and reduced type 1 (Th1) cytokine responses in C–C chemokine receptor 2 knockout mice. J. Clin. Invest. 100, 2552–2561 (1997).

    Article  CAS  Google Scholar 

  52. Cook, D.N. et al. CCR6 mediates dendritic cell localization, lymphocyte homeostasis, and immune responses in mucosal tissue. Immunity 12, 495–503 (2000).

    Article  CAS  Google Scholar 

  53. Van Rooijen, N. & Sanders, A. Liposome mediated depletion of macrophages: mechanism of action, preparation of liposomes and applications. J. Immunol. Methods 174, 83–93 (1994).

    Article  CAS  Google Scholar 

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Acknowledgements

Supported by the Association Francaise Contre le Cancer (F.G.), the German Research Foundation (F.T.), the National Institutes of Health (AI49653 to G.J.R., and CA32551 and CA26504 to E.R.S.), the American Society of Hematology (X.-M.D.) and the Leukemia and Lymphoma Society (X.-M.D.).

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Correspondence to Miriam Merad.

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Ginhoux, F., Tacke, F., Angeli, V. et al. Langerhans cells arise from monocytes in vivo. Nat Immunol 7, 265–273 (2006). https://doi.org/10.1038/ni1307

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