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天然化合物 2,3-丁二醇激活 NK 细胞细胞毒性。

Activation of NK cell cytotoxicity by the natural compound 2,3-butanediol.

机构信息

Department of Medical Biotechnology and Laboratory Science, College of Medicine, Chang Gung University, Taiwan, Republic of China.

出版信息

J Leukoc Biol. 2012 Oct;92(4):807-14. doi: 10.1189/jlb.0112024. Epub 2012 Jul 16.

Abstract

The natural compound 2,3-BTD has diverse physiological effects in a range of organisms, including acting as a detoxifying product of liver alcohol metabolism in humans and ameliorating endotoxin-induced acute lung injury in rats. In this study, we reveal that 2,3-BTD enhances NK cell cytotoxic activity in human pNK cells and NK92 cells. Treatment of NK cells with 2,3-BTD increased perforin expression in a dose-dependent manner. This was accompanied by elevated JNK and ERK1/2 MAPK activities and enhanced expression of NKG2D/NCRs, upstream signaling molecules of the MAPK pathways. The 2,3-BTD effect was inhibited by pretreatment with inhibitors of JNK (SP) or ERK1/2 (PD) or by depleting NKG2D/NCRs or JNK1 or ERK2 with siRNA. These results indicate that 2,3-BTD activates NK cell cytotoxicity by NKG2D/NCR pathways and represent the first report of the 2,3-BTD effect on activation of innate immunity cells.

摘要

2,3-BTD 是一种天然化合物,在多种生物体中具有多种生理作用,包括作为人类肝脏酒精代谢解毒的产物,以及改善大鼠内毒素诱导的急性肺损伤。在这项研究中,我们揭示了 2,3-BTD 增强了人源 pNK 细胞和 NK92 细胞的 NK 细胞细胞毒性活性。2,3-BTD 处理 NK 细胞可剂量依赖性地增加穿孔素的表达。这伴随着 JNK 和 ERK1/2 MAPK 活性的升高,以及 NKG2D/NCRs 的表达增强,NKG2D/NCRs 是 MAPK 途径的上游信号分子。用 JNK(SP)或 ERK1/2(PD)抑制剂预处理或用 siRNA 耗尽 NKG2D/NCRs 或 JNK1 或 ERK2 可抑制 2,3-BTD 的作用。这些结果表明,2,3-BTD 通过 NKG2D/NCR 途径激活 NK 细胞细胞毒性,这是 2,3-BTD 对先天免疫细胞激活作用的首次报道。

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