The mechanism of activation of NK-cell IFN-γ production by ligation of CD28

被引:11
作者
Cheung, JC
Koh, CY
Gordon, BE
Wilder, JA
Yuan, D [1 ]
机构
[1] Univ Texas, SW Med Ctr, Dept Pathol, Lab Mol Pathol, Dallas, TX 75235 USA
[2] Carolina Med Ctr, Dept Comparat Med, Charlotte, NC 28232 USA
关键词
NK cells; CD28; IFN-gamma; mRNA stability; Fc gamma RIII; IL-12;
D O I
10.1016/S0161-5890(99)00051-6
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We have investigated the mechanism by which anti-CD28 antibodies activates IFN-gamma production by murine NK cells. These studies reveal that engagement of CD28 alone by this antibody is a poor activator of this cytokine response. Effective stimulation requires simultaneous ligation of the receptor for Fc (Fc gamma RIII, CD16) which on its own is also a poor inducer of murine NK cells. The mechanism by which immobilized anti-CD28 increases IFN-gamma mRNA abundance involves both upregulation of transcription as well as induction of mRNA stabilization. However, the elevation of transcription is not as evident as that induced by IL-12 which, in contrast, does not induce message stabilization. Thus ligation of CD28 in the presence of IL-12 results in a synergistic increase in production of the cytokine. Using this assay we have also determined that immobilized anti-CD28 cannot induce resting NK cells to produce IFN-gamma. In contrast, the same cells can be induced by BCL1-C11 tumor cells that express high amounts of the CD28 ligand, B7-2. These studies provide important insights into the ability of cells bearing counter-receptor for CD28 to activate NK cell-cytokine production in vivo. (C) 1999 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:361 / 372
页数:12
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