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From the Departments of Oral and Maxillofacial Surgery
I,*
and Pathology,
Tohoku
University, Sendai, Japan; the Department of
Bacteriology,
Kinki University, Osaka-Sayama,
Japan; the Department of Molecular Preventive
Medicine,§
University of Tokyo, Tokyo, Japan;
and the Molecular/Cancer Biology Laboratory and Department of
Pathology,¶
Haartman Institute, University of
Helsinki, Helsinki, Finland
Our previous study demonstrated formation of T cell-dendritic cell (DC) clusters in inflamed dermis of intraorally autotransplanted skin flaps. Such T cell-DC clusters are supposed to be important for close interactions between T cells and DCs including the specific antigen presentation. Here we show the involvement of the macrophage-derived chemokine (MDC/CCL22) and its specific receptor CC chemokine receptor 4 (CCR4) in the formation of T cell-DC clusters. Reverse transcriptase-polymerase chain reaction analysis revealed high levels of mRNA expression for MDC and CCR4 in inflamed skin and neck lymph nodes (LNs), but not in normal skin. Immunohistochemically, MDC+ cells and CCR4+ cells were mainly located within the T cell-DC clusters both in the dermis of inflamed skin and the T cell area of LNs. MDC+ cells were identified to be DCs both in inflamed skin and LNs. The majority of CCR4+ cells were CD4+ T cells, accounting for approximately one-third of total CD4+ T cells in the inflamed skin. Our data suggest that the MDC-CCR4 system plays an important role in the formation of T cell-DC clusters both in inflamed skin and LNs.
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