Loureirin B, an essential component of Sanguis Draxonis, inhibits Kv1.3 channel and suppresses cytokine release from Jurkat T cells

被引:12
|
作者
Yin, Shijin [1 ,2 ]
Hu, Qinglan [1 ]
Luo, Jialie [2 ]
Li, Yuxin [1 ]
Lu, Chunlan [1 ]
Chen, Xuan [1 ]
Hu, Hongzhen [2 ]
机构
[1] South Cent Univ Nationalities, Coll Pharm, Wuhan 430074, Peoples R China
[2] Washington Univ, Sch Med, Dept Anesthesiol, Ctr Study Itch, St Louis, MO 63110 USA
来源
CELL AND BIOSCIENCE | 2014年 / 4卷
基金
美国国家卫生研究院;
关键词
Loureirin B; Sanguis draxonis; Kv1.3; channels; IL-2; EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS; ROOT GANGLION NEURONS; SMOOTH-MUSCLE-CELLS; DRAGONS BLOOD; MULTIPLE-SCLEROSIS; POTASSIUM CHANNELS; K+ CHANNEL; LYMPHOCYTE FUNCTION; THERAPEUTIC TARGET; INSULIN-RESISTANCE;
D O I
10.1186/2045-3701-4-78
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
Sanguis draxonis (SD), also known as "Dragon's Blood", is a traditional herb medicine that has been used to treat a variety of complications with unknown mechanisms. Recent studies show that SD displays immunosuppressive activities and improves symptoms of type I diabetes in animal models. However, the mechanisms underlying SD's immunosuppressive actions are not completely understood. The voltage-gated Kv1.3 channel plays a critical role in the pathogenesis of autoimmune diseases by regulating the functions of both T cells and B cells. Here we investigated the effect of SD and one of its active components loureirin B (LrB) on Kv1.3. Both SD and LrB inhibited Kv1.3-mediated currents, produced a membrane depolarization, and reduced Ca2+ influx in Jurkat T cells. In addition, application of LrB inhibited phytohemagglutinin (PHA)-induced IL-2 release from activated Jurkat T cells. Furthermore, point mutations in the selective filter region significantly reduced the inhibitory effect of LrB on Kv1.3. The results of these experiments provide evidence that LrB is a channel blocker of Kv1.3 by interacting with amino acid residues in its selective filter region. Direct inhibition of Kv1.3 in T cells by SD and LrB might be the cellular and molecular basis of SD-mediated immunosuppression.
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页数:8
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