DefinitionThis section has been translated automatically.
CD 209 (Cluster of Differentiation 209), aka DC-SIGN (acronym for: Dendritic Cell-Specific Intercellular adhesion molecule-3-Grabbing Non-integrin), is a protein that in humans is encoded by the CD209 gene located on chromosome 19p13.2. DC-SIGN is a C-type lectin receptor that is present on the surface of both macrophages and dendritic cells.
DC-SIGN on macrophages recognizes and binds with high affinity to N-glycans with high mannose content, a class of pathogen-associated molecular patterns (PAMPs) commonly found on viruses, bacteria and fungi. This binding interaction activates phagocytosis. On myeloid and preplasmacytoid dendritic cells, DC-SIGN mediates the rolling interactions of dendritic cells with the blood endothelium and the activation of CD4+ T cells as well as the recognition of pathogen haptens. DC-SIGN is a C-type lectin and has a high affinity for the ICAM3 molecule. CD209 plays a key role as a receptor for various ligands such as ICAM-2(CD102), ICAM-3, HIV-1 gp120.
It binds various microorganisms by recognizing highly mannose-containing glycoproteins on their envelopes and functions in particular as a receptor for various viruses such as HIV, hepatitis C and various filoviridae. Binding to DC-SIGN can promote the infection of T cells from dendritic cells by HIV and hepatitis C viruses. Thus, binding to DC-SIGN is an essential process for HIV infection. In addition to functioning as an adhesion molecule, recent studies have also shown that DC-SIGN can initiate innate immunity by modulating Toll-like receptors, although the detailed mechanism is not yet known. DC-SIGN, together with other C-type lectins, is involved in tumor recognition by dendritic cells. DC-SIGN is also a potential development target for a dendritic cell-based cancer vaccine.
Application: FACS, IHC (G)
LiteratureThis section has been translated automatically.
- Hantschke M et al. (2016) Immunohistologic techniques. In: L. Cerroni et al. Histopathology of the skin. Springer Verlag Berlin-Heidelberg pp. 26-33.
- Hu B ET AL: (2020) Blockade of DC- SIGN<sup>+</sup> Tumor-Associated Macrophages Reactivates Antitumor Immunity and Improves Immunotherapy in Muscle-Invasive Bladder Cancer. Cancer Res 80:1707-1719.
- Jarvis CM et al. (2019) Antigen structure affects cellular routing through DC-SIGN. Proc Natl Acad Sci U S A 116:14862-14867.
- Marzi A ET AL: (2004) DC-SIGN and DC-SIGNR interact with the glycoprotein of Marburg virus and the S protein of severe acute respiratory syndrome coronavirus. J Virol 78:12090-12095.
- Zhou T ET AL: (200&) DC-SIGN and immunoregulation. Cell Mol Immunol 4:279-283.