FEBS Letters · 1998 · 89 citations · 36 references
Life SciencesImmunologyMolecular BiologyInflammationMolecular ImmunologySignal TransductionChemokine SignalingCytokine BiologyImmune Cell PhysiologyImmune Cell SignalingInflammatory SignalingT Cell ActivationAntigen Presenting CellsCd4 Positive T CellsCd8 Positive T Cell Responses
We have cloned the murine CCR6 receptor and its ligand, the beta-chemokine mMIP-3alpha. Calcium mobilization assays performed with mCCR6 transfectants showed significant responses upon addition of mMIP-3alpha. Murine MIP-3alpha RNA is expressed in thymus, small intestine and colon, whereas mCCR6 RNA is expressed in spleen and lymph nodes. RT-PCR analysis of FACS-sorted lymphoid and antigen presenting cell subsets showed mCCR6 expression mainly in B cells, CD8- splenic dendritic cells and CD4+ T cells. The cloning and functional characterization of the mCCR6 and mMIP-3alpha will allow the study of the role of these proteins in mouse models of inflammation and immunity.
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