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

Journal of leukocyte biology (2012-07-18)
Hsin-Chih Lai, Chih-Jung Chang, Chun-Hung Yang, Ya-Jing Hsu, Chang-Chieh Chen, Chuan-Sheng Lin, Yu-Huan Tsai, Tsung-Teng Huang, David M Ojcius, Ying-Huang Tsai, Chia-Chen Lu
RESUMEN

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.

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Sigma-Aldrich
2,3-Butanediol, 98%
Sigma-Aldrich
(2R,3R)-(−)-2,3-Butanediol, 97%
Sigma-Aldrich
meso-2,3-Butanediol, 99%
Sigma-Aldrich
(2S,3S)-(+)-2,3-Butanediol, 97%