Li Qing, Kobayashi Maiko, Kawada Tomoyuki
Department of Hygiene and Public Health, Nippon Medical School, 1-1-5 Sendagi, Tokyo, Japan.
Toxicology. 2007 Sep 24;239(1-2):89-95. doi: 10.1016/j.tox.2007.06.100. Epub 2007 Jul 5.
We found previously that organophosphorus pesticides (OPs) significantly inhibited natural killer (NK) activity. To explore the mechanism of OP-induced inhibition of NK activity, we investigated whether OPs can induce apoptosis in NK cells in the present study. We used NK-92CI and NK-92MI cells, which are interleukin-2 independent human NK cell lines. NK-92CI and/or NK-92MI were treated with dichlorvos (DDVP) or chlorpyrifos (CP) at 0-100 ppm for 1-72 h at 37 degrees C in vitro. Apoptosis induced by DDVP and CP was determined by FITC-Annexin V staining and the intracellular level of active caspase-3 was analysed by flow cytometry. We found that DDVP and CP significantly induced apoptosis in NK-92CI and NK-92MI cells in a dose- and time-dependent manner. DDVP also induced an increase of intracellular active caspase-3 in NK-92CI in a dose- and time-dependent manner, and a caspase-3 inhibitor, Z-DEVD-FMK, significantly inhibited DDVP-induced apoptosis, suggesting that this apoptosis is partially mediated by activation of intracellular caspase-3. The pattern of apoptosis induced by CP differed from that induced by DDVP. CP showed a faster response than DDVP at higher doses; whereas, DDVP showed a slower, but stronger apoptosis-inducing ability than CP at lower doses. Moreover, the response to OPs differed between NK-92CI and NK-92MI cells, and NK-92CI was more sensitive to OPs than NK-92MI. This is similar to the inhibition of NK activity induced by DDVP, in which NK-92CI was more easily inhibited by DDVP than NK-92MI. Taken together, these findings suggest that OP-induced inhibition of NK activity may be at least partially mediated by OP-induced apoptosis in NK.
我们之前发现有机磷农药(OPs)能显著抑制自然杀伤(NK)细胞的活性。为探究OPs诱导NK细胞活性抑制的机制,在本研究中我们调查了OPs是否能诱导NK细胞凋亡。我们使用了NK-92CI和NK-92MI细胞,它们是白细胞介素-2非依赖型人NK细胞系。将NK-92CI和/或NK-92MI在体外37℃下用0至100 ppm的敌敌畏(DDVP)或毒死蜱(CP)处理1至72小时。通过FITC-Annexin V染色测定DDVP和CP诱导的凋亡,并通过流式细胞术分析细胞内活性半胱天冬酶-3的水平。我们发现DDVP和CP以剂量和时间依赖性方式显著诱导NK-92CI和NK-92MI细胞凋亡。DDVP还以剂量和时间依赖性方式诱导NK-92CI细胞内活性半胱天冬酶-3增加,并且半胱天冬酶-3抑制剂Z-DEVD-FMK显著抑制DDVP诱导的凋亡,这表明这种凋亡部分是由细胞内半胱天冬酶-3的激活介导的。CP诱导的凋亡模式与DDVP诱导的不同。在较高剂量下,CP显示出比DDVP更快的反应;而在较低剂量下,DDVP显示出比CP更慢但更强的凋亡诱导能力。此外,NK-92CI和NK-92MI细胞对OPs的反应不同,并且NK-92CI比NK-92MI对OPs更敏感。这与DDVP诱导的NK细胞活性抑制情况相似,其中NK-92CI比NK-92MI更容易被DDVP抑制。综上所述,这些发现表明OPs诱导的NK细胞活性抑制可能至少部分是由OPs诱导的NK细胞凋亡介导的。