[HTML][HTML] Modulation of the inhibitory receptor leukocyte Ig-like receptor 1 on human natural killer cells

NL Li, CL Davidson, A Humar, DN Burshtyn - Frontiers in immunology, 2011 - frontiersin.org
NL Li, CL Davidson, A Humar, DN Burshtyn
Frontiers in immunology, 2011frontiersin.org
Leukocyte Ig-like receptor 1 (LIR-1) is an inhibitory Ig superfamily receptor with broad
specificity for MHC-I expressed on leukocytes including natural killer (NK) andT cells. The
extent of LIR-1 expression on NK cells is quite disparate between donors but the regulation
of LIR-1 in NK cells is poorly understood. We examined expression profiles of LIR-1 on NK
and T lymphocytes in 11 healthy donors over 1 year. Four of the 11 donors demonstrated
substantial increases in LIR-1+ NK cells. High levels of LIR-1 expression were not correlated …
Leukocyte Ig-like receptor 1 (LIR-1) is an inhibitory Ig superfamily receptor with broad specificity for MHC-I expressed on leukocytes including natural killer (NK) andT cells. The extent of LIR-1 expression on NK cells is quite disparate between donors but the regulation of LIR-1 in NK cells is poorly understood. We examined expression profiles of LIR-1 on NK and T lymphocytes in 11 healthy donors over 1 year. Four of the 11 donors demonstrated substantial increases in LIR-1+ NK cells. High levels of LIR-1 expression were not correlated with exposure to human cytomegalovirus or the fraction of CD57+ NK cells in the donor. LIR-1 levels on ex vivo NK and CD56+ T cells were increased in vitro by short term exposure to IL-2 or IL-15 compared to control but not with various other cytokines tested. Sorted CD56bright NK cells also increased LIR-1 expression when cultured in IL-2. Maintenance of LIR-1 on longer term NK cells was also dependent on continuous stimulation by IL-15 or IL-2. While we could not detect increases in total LIR-1 mRNA in response to cytokine treatment by qPCR, we observed a shift in activity of LIR-1 promoter reporter constructs in the presence of IL-2 favoring the more translationally active transcript from the proximal promoter. Together these results show LIR-1 on NK cells is under the control of cytokines known to drive NK cell maturation and activation and suggest availability of such cytokines may alter the NK repertoire in vivo as we observed in several donors with fluctuating levels of LIR-1 on their NK cells.
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