Role of ChemR23 in directing the migration of myeloid and plasmacytoid dendritic cells to lymphoid organs and inflamed skin

J Exp Med. 2005 Feb 21;201(4):509-15. doi: 10.1084/jem.20041310.

Abstract

Chemerin is a chemotactic agent that was recently identified as the ligand of ChemR23, a serpentine receptor expressed by activated macrophages and monocyte-derived dendritic cells (DCs). This paper shows that blood plasmacytoid and myeloid DCs express functional ChemR23. Recombinant chemerin induced the transmigration of plasmacytoid and myeloid DCs across an endothelial cell monolayer. In secondary lymphoid organs (lymph nodes and tonsils), ChemR23 is expressed by CD123(+) plasmacytoid DCs and by CD1a(+) DC-SIGN(+) DCs in the interfollicular T cell area. ChemR23(+) DCs were also observed in dermis from normal skin, whereas Langerhans cells were negative. Chemerin expression was selectively detected on the luminal side of high endothelial venules in secondary lymphoid organs and in dermal endothelial vessels of lupus erythematosus skin lesions. Chemerin(+) endothelial cells were surrounded by ChemR23(+) plasmacytoid DCs. Thus, ChemR23 is expressed and functional in plasmacytoid DCs, a property shared only by CXCR4 among chemotactic receptors. This finding, together with the selective expression of the cognate ligand on the luminal side of high endothelial venules and inflamed endothelium, suggests a key role of the ChemR23/chemerin axis in directing plasmacytoid DC trafficking.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Movement
  • Cells, Cultured
  • Chemokines / biosynthesis
  • Chemokines / pharmacology
  • Chemotactic Factors / biosynthesis
  • Chemotactic Factors / pharmacology
  • Dendritic Cells / drug effects
  • Dendritic Cells / immunology
  • Dendritic Cells / physiology*
  • Endothelial Cells / drug effects
  • Humans
  • Intercellular Signaling Peptides and Proteins
  • Ligands
  • Lupus Erythematosus, Systemic / blood
  • Lupus Erythematosus, Systemic / immunology*
  • Lupus Erythematosus, Systemic / pathology
  • Lymphoid Tissue / blood supply*
  • Lymphoid Tissue / immunology
  • Lymphoid Tissue / metabolism
  • Myeloid Cells / immunology
  • Plasma Cells / immunology
  • Receptors, Chemokine / biosynthesis
  • Receptors, Chemokine / physiology*
  • Skin / blood supply*
  • Skin / immunology
  • Skin / metabolism
  • Skin / pathology
  • Venules / immunology
  • Venules / metabolism

Substances

  • CMKLR1 protein, human
  • Chemokines
  • Chemotactic Factors
  • Intercellular Signaling Peptides and Proteins
  • Ligands
  • RARRES2 protein, human
  • Receptors, Chemokine