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首页> 外文期刊>Immunology: An Official Journal of the British Society for Immunology >Immunosuppressive evidence of Tityus serrulatus toxins Ts6 and Ts15: insights of a novel K+ channel pattern in T cells
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Immunosuppressive evidence of Tityus serrulatus toxins Ts6 and Ts15: insights of a novel K+ channel pattern in T cells

机译:拟南芥毒素Ts6和Ts15的免疫抑制证据:T细胞中新型K +通道模式的见解

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The voltage-gated potassium channel Kv1.3 is a novel target for immunomodulation of autoreactive effector memory T cells, which play a major role in the pathogenesis of autoimmune diseases. In this study, the Ts6 and Ts15 toxins isolated from Tityus serrulatus (Ts) were investigated for their immunosuppressant roles on CD4(+) cell subsets: naive, effector (TEF), central memory (T-CM) and effector memory (T-EM). The electro-physiological assays confirmed that both toxins were able to block Kv1.3 channels. Interestingly, an extended Kv channel screening shows that Ts15 blocks Kv2.1 channels. Ts6 and Ts15 significantly inhibit the proliferation of T-EM cells and interferon-c production; however, Ts15 also inhibits other CD4(+) cell subsets (naive, TEF and T-CM). Based on the Ts15 inhibitory effect of proliferation of all CD4(+) cell subsets, and based on its blocking effect on Kv2.1, we investigated the Kv2.1 expression in T cells. The assays showed that CD4(+) and CD8(+) cells express the Kv2.1 channels mainly extracellularly with T-CM cells expressing the highest number of Kv2.1 channels. We also provide in vivo experimental evidence to the protective effect of Ts6 and Ts15 on delayed-type hypersensitivity reaction. Altogether, this study presents the immunosuppressive behaviour of Ts6 and Ts15 toxins, indicating that these toxins could be promising candidates for autoimmune disease therapy. Moreover, this is the first report illustrating the involvement of a novel K+ channel subtype, Kv2.1, and its distribution in T-cell subsets.
机译:电压门控钾通道Kv1.3是免疫反应性自身记忆T细胞的免疫调节的新目标,其在自身免疫性疾病的发病机理中起主要作用。在这项研究中,研究了从Tityus serrulatus(Ts)分离的Ts6和Ts15毒素对CD4(+)细胞亚群的免疫抑制作用:幼稚,效应物(TEF),中枢记忆(T-CM)和效应物记忆(T- EM)。电生理测定法证实两种毒素均能够阻断Kv1.3通道。有趣的是,扩展的Kv频道筛选显示Ts15会阻止Kv2.1频道。 Ts6和Ts15显着抑制T-EM细胞的增殖和干扰素c的产生;但是,Ts15还抑制其他CD4(+)细胞亚群(未用过的,TEF和T-CM)。基于所有CD4(+)细胞亚群的Ts15增殖抑制作用,并基于其对Kv2.1的阻断作用,我们研究了Kv2.1在T细胞中的表达。分析表明,CD4(+)和CD8(+)细胞主要在细胞外表达Kv2.1通道,而T-CM细胞则表达最高数量的Kv2.1通道。我们还提供体内实验证明Ts6和Ts15对迟发型超敏反应的保护作用。总之,这项研究提出了Ts6和Ts15毒素的免疫抑制行为,表明这些毒素可能是自身免疫疾病治疗的有希望的候选者。此外,这是第一份报告,阐明了新型K +通道亚型Kv2.1的参与及其在T细胞亚群中的分布。

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