A Potential Role for Interleukin-15 in the Regulation of Human Natural Killer Cell Survival


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Abstract

Resting lymphocyte survival is dependent upon the expression of Bcl-2, yet the factors responsible for maintaining lymphocyte Bcl-2 protein expression in vivo are largely unknown. Natural killer (NK) cells are bone marrow-derived lymphocytes that constitutively express the beta and common gammac subunits of the IL-2 receptor (R) as a heterodimer with intermediate affinity for IL-2, IL-15 also binds to IL-2R beta gammac and is much more abundant in normal tissues than IL-2. Mice that lack the IL-2 gene have NK cells, whereas mice and humans that lack IL-2R gammac do not have NK cells. Further, treatment of mice with an antibody directed against IL-2R beta results in a loss of the NK cell compartment. These data suggest that a cytokine other than IL-2, which binds to IL-2R beta gammac, is important for NK cell development and survival in vivo. In the current report, we show that the recently described IL-15R alpha subunit cooperates with IL-2R beta gammac to transduce an intracellular signal at picomolar concentrations of IL-15. We demonstrate that resting human NK cells express IL-15R alpha mRNA and further, that picomolar amounts of IL-15 can sustain NK cell survival for up to 8 d in the absence of serum. NK cell survival was not sustained by other monocyte-derived factors (i.e., TNF-alpha, IL-1 beta, IL-10, IL-12) nor by cytokines known to use gammac for signaling (i.e., IL-4, IL-7, IL-9, IL- 13). One mechanism by which IL-15 promotes NK cell survival may involve the maintenance of Bcl-2 protein expression. Considering these functional properties of IL-15 and the fact that it is produced by bone marrow stromal cells and activated monocytes, we propose that IL-15 may function as an NK cell survival factor in vivo. (J. Clin. Invest. 1997. 99:937-943.)

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