The role of chemerin in the co-localization of NK and dendritic cell subsets into inflamed tissues.

Chemerin is a chemotactic agonist recently identified as the ligand of
ChemR23, a serpentine receptor expressed by mononuclear phagocytes and
dendritic cells (DCs). This study shows that blood CD56lowCD16_ natural killer
(NK) cells selectively express functional ChemR23 and that this receptor is coexpressed
with CXCR1, the CXCL8 receptor, and the KIR receptors. In vitro culturing
of NK cells with IL-2 or IL-15 induced a delayed and time-dependent down-regulation
of ChemR23 that was associated with the inhibition of NK cell migration to
chemerin. Biopsies obtained from patients with oral lichen planus presented
an infiltration of CD94_CD3_CD56_ NK cells that coexpressed ChemR23. The
same biopsies were infiltrated by myeloid, DC-SIGN_ and plasmacytoid,
CD123_BDCA2_, ChemR23_ dendritic cells that were occasionally associated
with NK cells. In the same histologic sections, chemerin was expressed by inflamed
dermal endothelium. These findings propose a role for the ChemR23/
chemerin axis in the recruitment of blood NK cells and strongly implicate chemerin
as a key factor for the colocalization of NK cells and DC subsets in pathologic
peripheral tissues