Summary
The CD14 surface molecule is predominantly expressed by cells of myeloid origin and regarded as a specific marker for macrophages (Mø). Thus, in human mononuclear cell preparations, CD14 expression is a widely used parameter to distinguish Mø from dendritic cells (DC). Since a murine homologue of CD14 was recently identified, this study investigated expression of CD14 by murine Mø and DC. Flow cytometry with a monoclonal antibody directed against murine CD14 revealed that bone marrow-derived DC express CD14 to various extents during differentiation. Functionally, CD14high and CD14low DC did not differ significantly in their capacity to present alloantigen, protein antigen or immunogenic peptide. Furthermore, surface expression of CD14 could be modulated by interleukin (IL)-4 and LPS. Incubation of bone marrow-derived DC with IL-4 (100 U/ml) resulted in downregulation of CD14 surface expression, whereas exposure of BmDC to LPS (1 µg/ml) led to upregulation of CD14. After blockage of CD14 molecules by incubation of DC with anti-CD14 antibodies, downregulation of LPS triggered IL-1 release could be detected. In addition, other Mø markers such as CD11b, F4/80, BM8, and ER-TR9, are also expressed on DC. Therefore, we conclude that CD14, like other Mø markers, is expressed on murine DC during maturation. Thus, Mø and DC cannot be distinguished by flow cytometry using these markers. Moreover, CD14 may be involved in mediating LPS-induced activation of murine DC.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Preview
Unable to display preview. Download preview PDF.
Similar content being viewed by others
References
Todd, R.F., Nadler, L.M., Schlossman, S.F. (1981) Antigens on human monocytes identified by monoclonal antibodies. J. Immunol. 126, 1435–1442.
Ball, E.D., Graziano, R.F., Shen, L., Fanger, M.W. (1982) Monoclonal antibodies to novel myeloid antigens reveal human neutrophil heterogeneity. Proc. Natl. Acad. Sci. USA 79, 5374–5377.
Kielian, T.L., Blecha, F. (1995) CD14 and other recognition molecules for lipopolysaccharide: a review. Immunopharmacology 29, 187–205.
Wright, S.D. (1991) CD14 and immune response to lipopolysaccharide. Science (Wash. DC). 252, 1321–1325.
Wright, S.D., Ramos, R.A., Tobias, P.S., Ulevitch, R.J., Mathison, J.C. (1990) CD14, a receptor for complexes of lipopolysaccharide (LPS) and LPS binding protein. Science (Wash. DC) 249, 1431–1434.
Matsura, K., Ishida, T., Setoguchi, M., Higuchi, Y., Akizuki, S., Yamamoto, S. (1994) Upregulation of mouse CD14 expression in Kupffer cells by lipopolysaccharide. J. Exp. Med. 179, 1671–1676.
Ferrero, E., Hsieh, C.L., Francke, U., Goyert, S.M. (1990) CD14 is a member of the family of leucine-rich proteins and is encoded by a gene syntenic with multiple receptor genes. J. Immunol. 145, 331–336.
Steinman, R.M., Witmer-Pack, M., Inaba, K. (1993) Dendritic cells: antigen presentation, accessory function and clinical relevance. Adv. Exp. Med. Biol. 329, 1–9.
Inaba, K., Inaba, M., Deguchi, M., Hagi, K., Yasumizu, R., Ikehara, S., Muramatsu, S., Steinman, R.M. (1993) Granulocytes, macrophages, and dendritic cells arise from a common major histocompatibility complex class II-negative progenitor in mouse bone marrow. Proc Natl Acad Sci USA 90, 3038–42.
Peters, J.H., Gieseler, R., Thiele, B., Steinbach, F. (1996) Dendritic cells: from ontogenetic orphans to myelomonocytic descendants. Immunol. Today 17, 273–278.
Caux, C., Vanbervliet, B., Massacrier, C., Dezutter Dambuyant, C., de Saint Vis, B., Jacquet, C., Yoneda, K., Imamura, S., Schmitt, D., Banchereau, J. (1996) CD34’ hematopoietic progenitors from human cord blood differentiate along two independent dendritic cell pathways in response to GM-CSF plus TNFa. J. Exp. Med 184, 695–706.
Paglia, P., Girolomoni, G., Robbiati, F., Granucci, F., Ricciardi-Castagnoli, R. (1993) Immortalized dendritic cell line fully competent in antigen presentation initiates primary T cell responses in vivo. J. Exp. Med. 178, 1903–10.
Granucci, F., Girolomoni, G., Lutz, M.B., Foti, M., Marconi, G., Gnocchi, R, Nolli, L., Ricciardi Castagnoli, P. (1994) Modulation of cytokine expression in mouse dendritic cell clones. Eur. J. Immunol 24, 2522–6.
Xu, S., Ariizumi, K., Caceres, D.G., Edelbaum, D., Hashimoto, K., Bergstresser, P.R., Takashima, A. (1995) Successive generation of antigen-presenting, dendritic cell lines from murine epidermis. J Immunol 154, 2697–705.
Scheicher, C., Mehlig, M., Zecher, R., Reske, K. (1992) Dendritic cells from bone marrow: in vitro differentiation using low doses of recombinant granulocyte-macrophage colony stimulating factor. J. Immunol. Meth. 154, 153–264.
Inaba, K., Inaba, M., Romani, N., Aya, H., Deguchi, M., Ikehara, S., Muramatsu, S., Steinman, R. (1992) Generation of large numbers of dendritic cells from mouse bone marrow cultures supplemented with granulocyte/macrophage colony stimulating factor. J. Exp. Med. 176, 1693–1702.
S. Grabbe, K. Steinbrink, M. Steinert, T.A. Luger, T. Schwarz. 1995. Removal of the majority of epidermal Langerhans cells by topical or systemic steroid application enhances the effector phase of murine contact hypersensitivity. J. Immunol. 155: 4207–4217.
Ruppert, J., Peters, J.H. (1991) Accessory cell function during monocyte/macrophage differentiation: relation to interleukin-1 (IL-1 beta) production and release. EurJ Cell Bio1 55, 352–61.
Romani, N., Lenz, A., Glassel, H., Stossel, H., Stanzl, U., Majdic, O., Fritsch, R, Schuler, G. (1989) Cultured human Langerhans cells resemble lymphoid dendritic cells in phenotype and function. J. Invest. Dermatol. 93, 600–609.
Sallusto, F., Lanzavecchia, A. (1994) Efficient presentation of soluble antigen by cultured human dendritic cells is maintained by granulocyte/macrophage colony-stimulating factor plus interleukin 4 and down-regulated by tumor necrosis factor alpha. J. Exp. Med. 179, 1109–18.
Steinman, R.M. (1991) The dendritic cell system and its role in immunogenicity. Annu. Rev. Immunol. 9, 271–296.
Greame-Cook, F., Bhan, A.K., Harris, N.L. (1993) Immunohistochemical characterization of intraepithelial and subepithelial mononuclear cells of the upper airways. Am. J. Pathol. 143, 1416–1422.
O“Doherty, U., M. Peng, S. Gezelter, W. J. Swiggard, M. Betjes, N. Bhardwaj, and R. M. Steinman. (1994) Human blood contains two subsets of dendritic cells, one immunologically mature and the other immature. Immunology 82, 487–493.
Thomas, R., and R. E. Lipsky (1994) Human peripheral blood dendritic cell subsets. Isolation and characterisation of precursor and mature antigen-presenting cells. J. Immunol. 153, 4016–4027.
Zhou, L.J., Tedder, T.F. (1996) CD14* blood monocytes can differentiate into functionally mature CD83’ dendritic cells. Proc. Natl. Acad. Sci. USA. 93, 2588–92
Ruppert, J., Friedrichs, D., Xu, H., Peters, J.H. (1991) IL-4 decreases the expression of monocyte differentiation marker CDI4, paralleled by an increasing accessory potency. Immunobiology 182, 449–464.
Bazil, V., Strominger, J.L. (1991) Shedding as a mechanism of down-modulation of CD14 on stimulated human monocytes. J. Immunol. 147, 1567–1571.
Roake, J.A., Rao, A.S., Morris, P.J., Larsen, C.P., Hankins, D.F., Austyn, J.M. (1995) Dendritic cell loss from nonlymphoid tissues after systemic administration of lipopolysaccharide, tumor necrosis factor, and interleukin 1. J. Exp. Med. 181, 2237–2247.
Couturier, C., Jahns, G., Kazatchine, M., Haefner-Cavaillon, N. (1992) Membrane molecules which trigger the production of interleukin-I and tumor necrosis factor-a by lipopolysaccharide-stimulated human monocytes. Eur J. Immunol. 22, 1461–1466.
Author information
Authors and Affiliations
Corresponding author
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 1997 Springer Science+Business Media New York
About this chapter
Cite this chapter
Mahnke, K., Becher, E., Ricciardi-Castagnoli, P., Luger, T.A., Schwarz, T., Grabbe, S. (1997). CD14 is Expressed by Subsets of Murine Dendritic Cells and Upregulated by Lipopolysaccharide. In: Ricciardi-Castagnoli, P. (eds) Dendritic Cells in Fundamental and Clinical Immunology. Advances in Experimental Medicine and Biology, vol 417. Springer, Boston, MA. https://doi.org/10.1007/978-1-4757-9966-8_25
Download citation
DOI: https://doi.org/10.1007/978-1-4757-9966-8_25
Publisher Name: Springer, Boston, MA
Print ISBN: 978-1-4757-9968-2
Online ISBN: 978-1-4757-9966-8
eBook Packages: Springer Book Archive