CC-chemokine receptor 6 is expressed on diverse memory subsets of T cells and determines responsiveness to macrophage inflammatory protein 3α

F Liao, RL Rabin, CS Smith, G Sharma… - The Journal of …, 1999 - journals.aai.org
F Liao, RL Rabin, CS Smith, G Sharma, TB Nutman, JM Farber
The Journal of Immunology, 1999journals.aai.org
Abstract CC-chemokine receptor (CCR) 6 is the only known receptor for macrophage
inflammatory protein (MIP)-3α, a CC chemokine chemotactic for lymphocytes and dendritic
cells. Using anti-serum that we raised against the N-terminal residues of CCR6, we have
characterized the surface expression of CCR6 on peripheral blood leukocytes and we have
correlated CCR6 expression with responses to MIP-3α. We found that CCR6 was expressed
only on memory T cells, including most α 4 β 7 memory cells and cutaneous lymphocyte …
Abstract
CC-chemokine receptor (CCR) 6 is the only known receptor for macrophage inflammatory protein (MIP)-3α, a CC chemokine chemotactic for lymphocytes and dendritic cells. Using anti-serum that we raised against the N-terminal residues of CCR6, we have characterized the surface expression of CCR6 on peripheral blood leukocytes and we have correlated CCR6 expression with responses to MIP-3α. We found that CCR6 was expressed only on memory T cells, including most α 4 β 7 memory cells and cutaneous lymphocyte-associated Ag-expressing cells, and on B cells. Accordingly, chemotaxis of T cells to MIP-3α was limited to memory cells. Moreover, calcium signals on T cells in response to MIP-3α were confined to CCR6-expressing cells, consistent with CCR6 being the only MIP-3α receptor on peripheral blood T cells. Unlike many CC chemokines, MIP-3α produced a calcium signal on freshly isolated T cells, and CCR6 expression was not increased by up to 5 days of treatment with IL-2 or by cross-linking CD3. Despite their surface expression of CCR6, freshly isolated B cells did not respond to MIP-3α. In addition to staining peripheral blood leukocytes, our anti-serum detected CCR6 on CD34+ bone marrow cell-derived dendritic cells. Our data are the first to analyze surface expression of CCR6, demonstrating receptor expression on differentiated, resting memory T cells, indicating differences in receptor signaling on T cells and B cells and suggesting that CCR6 and MIP-3α may play a role in the physiology of resting memory T cells and in the interactions of memory T cells, B cells, and dendritic cells.
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