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Among FITC + cells, Langerin + Langerhans cells and Langerin − (dermal) dDC subsets were detected as CD11c high+CD11b int+ cells and CD11c high+CD11b high+ plus CD11c low+CD11b int+ cells, respectively, both of which were suppressed by CXCR4 antagonist.
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FITC-induced cutaneous DC migration into the draining lymph nodes was impaired by the specific CXCR4 antagonist 4-F-Benzoyl-TN14003. Initially, we found that CXCR4 was highly expressed on migrated cutaneous DCs and that its ligand, CXCL12, was detected in the LYVE-1 + lymphatic vessels in the skin. However, complete migratory inhibition cannot be obtained in CCR7-deficient mice, suggesting that there exist other chemokine receptors involved in this process.
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