Fig. 1.
Extracellular ATP induces CCR7 and CXCR4 and down-regulates CCR5 mRNA.
DCs were generated from purified peripheral blood CD14+monocytes by culture with granulocyte-macrophage colony-stimulating factor and IL-4. On day 6, CD2+ and CD19+ cells were removed; resulting cells were more than 97% CD1a+ and CD14−. Immature DCs were not treated (nt), stimulated with 250 μM ATP or UTP, or induced to mature with 10 μg/mL LPS in the absence or presence of nucleotides. After 16 hours, total RNA was extracted and RNase protection assay done to visualize chemokine-receptor mRNA transcripts. Shown is one representative experiment of 3 done.