Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • Article
  • Published:

Activation of bone marrow–resident memory T cells by circulating, antigen-bearing dendritic cells

Abstract

Dendritic cells (DCs) carry antigen from peripheral tissues via lymphatics to lymph nodes. We report here that differentiated DCs can also travel from the periphery into the blood. Circulating DCs migrated to the spleen, liver and lung but not lymph nodes. They also homed to the bone marrow, where they were retained better than in most other tissues. Homing of DCs to the bone marrow depended on constitutively expressed vascular cell adhesion molecule 1 and endothelial selectins in bone marrow microvessels. Two-photon intravital microscopy in bone marrow cavities showed that DCs formed stable antigen-dependent contacts with bone marrow–resident central memory T cells. Moreover, using this previously unknown migratory pathway, antigen-pulsed DCs were able to trigger central memory T cell–mediated recall responses in the bone marrow.

This is a preview of subscription content, access via your institution

Access options

Buy this article

Prices may be subject to local taxes which are calculated during checkout

Figure 1: In vivo migration pathways of immature and mature DCs.
Figure 2: DCs traffic constitutively to bone marrow.
Figure 3: Molecular mechanism of the homing of DCs to bone marrow.
Figure 4: DCs that have homed induce antigen-specific TCM cell proliferation in the bone marrow.
Figure 5: Two-photon microscopy analysis of TCM cell–DC interactions and motility in skull bone marrow.

Similar content being viewed by others

References

  1. Banchereau, J. et al. Immunobiology of dendritic cells. Annu. Rev. Immunol. 18, 767–811 (2000).

    Article  CAS  Google Scholar 

  2. Cavanagh, L.L. & von Andrian, U.H. Travellers in many guises: The origins and destinations of dendritic cells. Immunol. Cell Biol. 80, 448–462 (2002).

    Article  Google Scholar 

  3. Sallusto, F. et al. Rapid and coordinated switch in chemokine receptor expression during dendritic cell maturation. Eur. J. Immunol. 28, 2760–2769 (1998).

    Article  CAS  Google Scholar 

  4. Balazs, M., Martin, F., Zhou, T. & Kearney, J. Blood dendritic cells interact with splenic marginal zone B cells to initiate T-independent immune responses. Immunity 17, 341–352 (2002).

    Article  CAS  Google Scholar 

  5. Randolph, G.J., Inaba, K., Robbiani, D.F., Steinman, R.M. & Muller, W.A. Differentiation of phagocytic monocytes into lymph node dendritic cells in vivo. Immunity 11, 753–761 (1999).

    Article  CAS  Google Scholar 

  6. Legge, K.L. & Braciale, T.J. Accelerated migration of respiratory dendritic cells to the regional lymph nodes is limited to the early phase of pulmonary infection. Immunity 18, 265–277 (2003).

    Article  CAS  Google Scholar 

  7. Mullins, D.W. et al. Route of immunization with peptide-pulsed dendritic cells controls the distribution of memory and effector T cells in lymphoid tissues and determines the pattern of regional tumor control. J. Exp. Med. 198, 1023–1034 (2003).

    Article  CAS  Google Scholar 

  8. Schuler, G., Schuler-Thurner, B. & Steinman, R.M. The use of dendritic cells in cancer immunotherapy. Curr. Opin. Immunol. 15, 138–147 (2003).

    Article  CAS  Google Scholar 

  9. Sallusto, F., Geginat, J. & Lanzavecchia, A. Central memory and effector memory T cell subsets: function, generation, and maintenance. Annu. Rev. Immunol. 22, 745–763 (2004).

    Article  CAS  Google Scholar 

  10. Di Rosa, F. & Santoni, A. Bone marrow CD8 T cells are in a different activation state than those in lymphoid periphery. Eur. J. Immunol. 32, 1873–1880 (2002).

    Article  CAS  Google Scholar 

  11. Becker, T.C., Coley, S.M., Wherry, E.J. & Ahmed, R. Bone marrow is a preferred site for homeostatic proliferation of memory CD8 T cells. J. Immunol. 174, 1269–1273 (2005).

    Article  CAS  Google Scholar 

  12. Mazo, I.B. et al. Bone marrow is a major reservoir and site of recruitment for central memory CD8+ T cells. Immunity 22, 259–270 (2005).

    Article  CAS  Google Scholar 

  13. Feuerer, M. et al. Therapy of human tumors in NOD/SCID mice with patient-derived reactivated memory T cells from bone marrow. Nat. Med. 7, 452–458 (2001).

    Article  CAS  Google Scholar 

  14. Maraskovsky, E. et al. Dramatic increase in the numbers of functionally mature dendritic cells in Flt3 ligand-treated mice: multiple dendritic cell subpopulations identified. J. Exp. Med. 184, 1953–1962 (1996).

    Article  CAS  Google Scholar 

  15. Mora, J.R. et al. Selective imprinting of gut-homing T cells by Peyer's patch dendritic cells. Nature 424, 88–93 (2003).

    Article  CAS  Google Scholar 

  16. von Andrian, U.H. & Mackay, C.R. T-cell function and migration. Two sides of the same coin. N. Engl. J. Med. 343, 1020–1034 (2000).

    Article  CAS  Google Scholar 

  17. Shortman, K. & Liu, Y.J. Mouse and human dendritic cell subtypes. Nat. Rev. Immunol. 2, 151–161 (2002).

    Article  CAS  Google Scholar 

  18. Donnenberg, V.S. et al. Rare-event analysis of circulating human dendritic cell subsets and their presumptive mouse counterparts. Transplantation 72, 1946–1951 (2001).

    Article  CAS  Google Scholar 

  19. Wright, D.E., Wagers, A.J., Gulati, A.P., Johnson, F.L. & Weissman, I.L. Physiological migration of hematopoietic stem and progenitor cells. Science 294, 1933–1936 (2001).

    Article  CAS  Google Scholar 

  20. Kamath, A.T. et al. The development, maturation, and turnover rate of mouse spleen dendritic cell populations. J. Immunol. 165, 6762–6770 (2000).

    Article  CAS  Google Scholar 

  21. Mazo, I.B. et al. Hematopoietic progenitor cell rolling in bone marrow microvessels: Parallel contributions by endothelial selectins and VCAM-1. J. Exp. Med. 188, 465–474 (1998).

    Article  CAS  Google Scholar 

  22. Manjunath, N. et al. Effector differentiation is not prerequisite for generation of memory cytotoxic T lymphocytes. J. Clin. Invest. 108, 871–878 (2001).

    Article  CAS  Google Scholar 

  23. Weninger, W., Crowley, M.A., Manjunath, N. & von Andrian, U.H. Migratory properties of naive, effector, and memory CD8+ T cells. J. Exp. Med. 194, 953–966 (2001).

    Article  CAS  Google Scholar 

  24. Robert, C. et al. Gene therapy to target dendritic cells from blood to lymph nodes. Gene Ther. 10, 1479–1486 (2003).

    Article  CAS  Google Scholar 

  25. Sumen, C., Mempel, T.R., Mazo, I.B. & von Andrian, U.H. Intravital microscopy; visualizing immunity in context. Immunity 21, 315–329 (2004).

    CAS  Google Scholar 

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

    Article  Google Scholar 

  27. O'Keeffe, M. et al. Dendritic cell precursor populations of mouse blood: identification of the murine homologues of human blood plasmacytoid pre-DC2 and CD11c+ DC1 precursors. Blood 101, 1453–1459 (2003).

    Article  CAS  Google Scholar 

  28. Robert, C. et al. Interaction of dendritic cells with skin endothelium: A new perspective on immunosurveillance. J. Exp. Med. 189, 627–636 (1999).

    Article  CAS  Google Scholar 

  29. Fossum, S. Lymph-borne dendritic leucocytes do not recirculate, but enter the lymph node paracortex to become interdigitating cells. Scand. J. Immunol. 27, 97–105 (1988).

    Article  CAS  Google Scholar 

  30. Kupiec-Weglinski, J.W., Austyn, J.M. & Morris, P.J. Migration patterns of dendritic cells in the mouse. Traffic from the blood, and T cell-dependent and -independent entry to lymphoid tissues. J. Exp. Med. 167, 632–645 (1988).

    Article  CAS  Google Scholar 

  31. Lappin, M.B. et al. Analysis of mouse dendritic cell migration in vivo upon subcutaneous and intravenous injection. Immunology 98, 181–188 (1999).

    Article  CAS  Google Scholar 

  32. Frenette, P.S., Subbarao, S., Mazo, I.B., von Andrian, U.H. & Wagner, D.D. Endothelial selectins and vascular cell adhesion molecule-1 promote hematopoietic progenitor homing to bone marrow. Proc. Natl. Acad. Sci. USA 95, 14423–14428 (1998).

    Article  CAS  Google Scholar 

  33. Di Rosa, F. & Pabst, R. The bone marrow: a nest for migratory memory T cells. Trends Immunol. 26, 360–366 (2005).

    Article  CAS  Google Scholar 

  34. Wherry, E.J. et al. Lineage relationship and protective immunity of memory CD8 T cell subsets. Nat. Immunol. 4, 225–234 (2003).

    Article  CAS  Google Scholar 

  35. Zammit, D.J., Cauley, L.S., Pham, Q.M. & Lefrancois, L. Dendritic cells maximize the memory CD8 T cell response to infection. Immunity 22, 561–570 (2005).

    Article  CAS  Google Scholar 

  36. Mempel, T.R., Henrickson, S.E. & von Andrian, U.H. T cell priming by dendritic cells in lymph nodes occurs in three distinct phases. Nature 427, 154–159 (2004).

    Article  CAS  Google Scholar 

  37. Gesner, B.M. & Gowans, J.L. The output of lymphocytes from the thoracic duct of unanaesthetized mice. Br. J. Exp. Path. 43, 424–430 (1962).

    CAS  Google Scholar 

  38. von Andrian, U.H. & Mempel, T.R. Homing and cellular traffic in lymph nodes. Nat. Rev. Immunol. 3, 867–878 (2003).

    Article  CAS  Google Scholar 

  39. Randolph, G.J., Beaulieu, S., Lebecque, S., Steinman, R.M. & Muller, W.A. Differentiation of monocytes into dendritic cells in a model of transendothelial trafficking. Science 282, 480–483 (1998).

    Article  CAS  Google Scholar 

  40. Enioutina, E.Y., Visic, D. & Daynes, R.A. The induction of systemic and mucosal immune responses to antigen-adjuvant compositions administered into the skin: alterations in the migratory properties of dendritic cells appears to be important for stimulating mucosal immunity. Vaccine 18, 2753–2767 (2000).

    Article  CAS  Google Scholar 

  41. Racanelli, V., Behrens, S.E., Aliberti, J. & Rehermann, B. Dendritic cells transfected with cytopathic self-replicating RNA induce crosspriming of CD8+ T cells and antiviral immunity. Immunity 20, 47–58 (2004).

    Article  CAS  Google Scholar 

  42. Larsen, C.P., Morris, P.J. & Austyn, J.M. Migration of dendritic leukocytes from cardiac allografts into host spleens. A novel pathway for initiation of rejection. J. Exp. Med. 171, 307–314 (1990).

    Article  CAS  Google Scholar 

  43. Saiki, T., Ezaki, T., Ogawa, M. & Matsuno, K. Trafficking of host- and donor-derived dendritic cells in rat cardiac transplantation: allosensitization in the spleen and hepatic nodes. Transplantation 71, 1806–1815 (2001).

    Article  CAS  Google Scholar 

  44. Vazquez-Torres, A. et al. Extraintestinal dissemination of Salmonella by CD18-expressing phagocytes. Nature 401, 804–808 (1999).

    Article  CAS  Google Scholar 

  45. Pircher, H., Burki, K., Lang, R., Hengartner, H. & Zinkernagel, R.M. Tolerance induction in double specific T-cell receptor transgenic mice varies with antigen. Nature 342, 559–561 (1989).

    Article  CAS  Google Scholar 

  46. Koni, P.A. et al. Conditional vascular cell adhesion molecule 1 deletion in mice. Impaired lymphocyte migration to bone marrow. J. Exp. Med. 193, 741–754 (2001).

    Article  CAS  Google Scholar 

  47. Boggs, D.R. The total marrow mass of the mouse: a simplified method of measurement. Am. J. Hematol. 16, 277–286 (1984).

    Article  CAS  Google Scholar 

  48. Boak, J.L. & Woodruff, M.F.A. Modified technique for collecting mouse thoracic duct lymph. Nature 205, 396–397 (1965).

    Article  CAS  Google Scholar 

  49. Lyons, A.B. Analysing cell division in vivo and in vitro using flow cytometric measurement of CFSE dye dilution. J. Immunol. Methods 243, 147–154 (2000).

    Article  CAS  Google Scholar 

  50. Mempel, T.R., Scimone, M.L., Mora, J.R. & von Andrian, U.H. In vivo imaging of leukocyte trafficking in blood vessels and tissues. Curr. Opin. Immunol. 16, 406–417 (2004).

    Article  CAS  Google Scholar 

Download references

Acknowledgements

We thank A. Vazquez-Torres (University of Colorado) for mutant strains of salmonella; G. Cheng and B. Reinhardt for technical support; and L. Scimone for help with intravital microscopy analysis. Supported by National Institutes of Health (AI061663, HL62524, HL54936 and HL56949 to U.H.v.A.); an Amy Potter fellowship, the Charles Hood Foundation and the Multiple Myeloma Foundation (I.B.M.); and Federazione Italiana Ricerca sul Cancro (R.B.).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Ulrich H von Andrian.

Ethics declarations

Competing interests

The authors declare no competing financial interests.

Supplementary information

Supplementary Video 1

Representative 3D time-lapse movie generated by 2-photon intravital microscopy in the skull of an anesthetized mouse. Hoechst 33342-labeled (blue) P14 TCM were injected into recipient mice and allowed to distribute in the body. 18h later, CMTMR-labeled (red) purified spleen DC were injected i.v. without peptide pulsing. Two hours thereafter, the animal was prepared for 2-photon intravital microscopy of skull BM as described in Materials and Methods. The luminal compartment of BM microvessels was delineated by i.v. injection of FITC-dextran (2MDa). 3D image stacks (23 optical sections, 5 µm vertical step size) were acquired every minute during a 30 min scan period. The total imaged volume (w x l x d) was 210 µm x 210 µm x 110 µm. (MOV 2880 kb)

Supplementary Video 2

Representative 3D time-lapse movie generated as described for movie 1, except that DC were pulsed with antigenic gp33 peptide prior to injection. Note that most TCM move at reduced velocity and undergo long-lasting tight contacts with DC. (MOV 2936 kb)

Rights and permissions

Reprints and permissions

About this article

Cite this article

Cavanagh, L., Bonasio, R., Mazo, I. et al. Activation of bone marrow–resident memory T cells by circulating, antigen-bearing dendritic cells. Nat Immunol 6, 1029–1037 (2005). https://doi.org/10.1038/ni1249

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1038/ni1249

This article is cited by

Search

Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing