Human natural killer cells produce abundant macrophage inflammatory protein-1 in response to monocyte-derived cytokines

被引:114
|
作者
Bluman, EM
Bartynski, KJ
Avalos, BR
Caligiuri, MA
机构
[1] ROSWELL PK CANC INST,DEPT HEMATOL & BONE MARROW TRANSPLANTAT,DIV MED,BUFFALO,NY 14263
[2] ROSWELL PK CANC INST,DEPT MOLEC MED,BUFFALO,NY 14263
[3] ROSWELL PK CANC INST,DEPT MOLEC IMMUNOL,BUFFALO,NY 14263
[4] OHIO STATE UNIV HOSP,DEPT INTERNAL MED,DIV BONE MARROW TRANSPLANTAT,COLUMBUS,OH 43210
[5] OHIO STATE UNIV HOSP,DEPT INTERNAL MED,DIV HEMATOL & ONCOL,COLUMBUS,OH 43210
关键词
chemokine; innate immunity; IL-15; IL-12; monokine;
D O I
10.1172/JCI118726
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Once infected by obligate intracellular pathogens, monocytes/macrophages release cytokines that activate natural killer (NK) cells, NK cells in turn produce and secrete monocyte/macrophage activating factors such as interferon-gamma (IFN-gamma), which are important in the early control of these infections, Here we demonstrate that human NK cells are potent producers of another monocyte/macrophage-activating factor, macrophage inflammatory protein-1 alpha (MIP-1 alpha). Fresh NK cells produce negligible amounts of MIP-1 alpha after stimulation with the monocyte-derived cytokines IL-12, TNF-alpha, IL-1 beta, or IL-10, while stimulation with IL-15 alone results in modest MIP-1 alpha production, Abundant NK cell production of MIP-1 alpha is seen after costimulation with IL-12 and IL-15, and is dose-dependent, Combinations of IL-12 with TNF-alpha, IL-1 beta, or IL-10 are substantially less effective inducers of MIP-1 alpha production by NK cells, NK cell MIP-1 alpha mRNA transcripts were detectable within 1 h after costimulation with IL-12 plus IL-15 and steadily increased over 24 h, with a concomitant increase in protein production detectable at 12 h, Resting NK cells constitutively express mRNA transcript for a MIP-1 alpha receptor, and costimulation with IL-12 and IL-15 upregulates its level of expression. Equilibrium binding studies with radioiodinated MIP-1 alpha were consistent with the induction of a single class of high affinity MIP-1 alpha receptors on NK cells costimulated with IL-12 and IL-15, Addition of exogenous MIP-1 alpha to resting NK cells did not enhance cytokine production but did increase NK cytotoxic activity, The requirement for IL-15 as a critical cofactor for NK cell production of MIP-1 alpha suggests a potentially unique role for this monocyte-derived cytokine in combination with IL-12. As MIP-1 alpha is known to potentiate the actions of IFN-gamma on monocytes and to suppress human immunodeficiency virus replication, the NK cell's production of MIP-1 alpha may be important during the innate immune response to infection.
引用
收藏
页码:2722 / 2727
页数:6
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