Expression and functional role of dipeptidyl peptidase IV (CD26) on human natural killer cells.

Natural immunity Pub Date : 1994-09-01
F Bühling, D Kunz, D Reinhold, A J Ulmer, M Ernst, H D Flad, S Ansorge
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Abstract

The expression and functional role of dipeptidyl peptidase IV (DP IV, CD26, EC 3.4.14.5) was studied on human natural killer (NK) cells. Here we show that freshly isolated NK cells do express only low amounts of DP IV. However, after IL-2 stimulation of NK cells (70% purity) surface DP IV expression was significantly increased in a subpopulation (30%) of these cells. Specific DP IV inhibitors (Lys-[Z-(NO2)]-piperidide, Lys-[Z(NO2)]-thiazolidide) and polyclonal antibodies directed against the ectopeptidase suppressed DNA synthesis and cell cycle progression of NK cells. The natural cytotoxic activity of DP IV+ CD56+ cells was found unchanged in comparison to those of DP IV- CD56+ cells. DP IV inhibitors had no effect on the natural cytotoxicity of mononuclear cells. From these data we conclude that DP IV is involved in the regulation of proliferation of NK cells, whereas natural cytotoxicity seems to be regulated independently.

二肽基肽酶IV (CD26)在人自然杀伤细胞中的表达及功能作用。
研究了二肽基肽酶IV (dipeptidyl peptidase IV, CD26, EC 3.4.14.5)在人自然杀伤(NK)细胞中的表达及其功能作用。在这里,我们发现新分离的NK细胞只表达少量的DP IV。然而,在IL-2刺激NK细胞(纯度为70%)后,这些细胞的一个亚群(30%)表面DP IV表达显著增加。特异性DP IV抑制剂(Lys-[Z-(NO2)]-piperidide, Lys-[Z(NO2)]-thiazolidide)和针对外肽酶的多克隆抗体抑制NK细胞的DNA合成和细胞周期进展。与DP IV- CD56+细胞相比,DP IV+ CD56+细胞的天然细胞毒活性没有变化。DP IV抑制剂对单核细胞的天然细胞毒性无影响。从这些数据我们得出结论,DP IV参与NK细胞增殖的调节,而天然细胞毒性似乎是独立调节的。
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