Publication | Open Access
Molecular cloning, functional characterization and mRNA expression analysis of the murine chemokine receptor CCR6 and its specific ligand MIP‐3α<sup>1</sup>
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Citations
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References
1998
Year
Murine Mip-3alpha RnaChemokine BiologyImmunologyImmunologic MechanismCd4 T Cell ResponsesImmune SystemInflammationSignaling PathwayCalcium Mobilization AssaysMurine Ccr6 ReceptorCell SignalingMrna Expression AnalysisReceptor (Biochemistry)T Cell ImmunityMolecular CloningCell BiologyMolecular ImmunologySignal TransductionFunctional CharacterizationCellular Immune ResponseMedicine
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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