钙、NF-κB和NFAT在Jurkat t细胞CXCL8和IL-6表达调控中的作用。

International journal of biochemistry and molecular biology Pub Date : 2013-09-13 eCollection Date: 2013-01-01
Hazem Khalaf, Jana Jass, Per-Erik Olsson
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引用次数: 0

摘要

t细胞在宿主抵抗入侵病原体的免疫中起着重要作用。确定潜在的调节机制将有助于更好地理解t细胞衍生的免疫反应。在这项研究中,我们发现NF-κB和NFAT在Jurkat t细胞中对IL-6和CXCL8的差异调节,以响应PMA、热杀伤大肠杆菌和钙。CXCL8与NFAT的激活模式密切相关,而IL-6的表达与NF-κB相关。此外,通过钙离子载体处理细胞增加细胞内Ca(2+)浓度可诱导NFAT,但不影响NF-κB活性。有趣的是,热激活NF-κB可杀死大肠杆菌,添加钙离子载体后,CXCL8和IL-6的表达被显著抑制。这表明钙在调节蛋白质运输和t细胞信号传导中起着重要作用,随后的炎症基因表达推断NFAT参与了CXCL8的调节。了解这些调节模式可以澄清细胞内信号传导改变导致t细胞衍生细胞因子表达的条件。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The role of calcium, NF-κB and NFAT in the regulation of CXCL8 and IL-6 expression in Jurkat T-cells.

T-cells play an important role in host immunity against invading pathogens. Determining the underlying regulatory mechanisms will provide a better understanding of T-cell-derived immune responses. In this study, we have shown the differential regulation of IL-6 and CXCL8 by NF-κB and NFAT in Jurkat T-cells, in response to PMA, heat killed Escherichia coli and calcium. CXCL8 was closely associated with the activation pattern of NFAT, while IL-6 expression was associated with NF-κB. Furthermore, increasing the intracellular Ca(2+) concentration by calcium ionophore treatment of the cells resulted in NFAT induction without affecting the NF-κB activity. Interestingly, NF-κB activation by heat killed E. coli, as well as CXCL8 and IL-6 expression was significantly suppressed following addition of the calcium ionophore. This indicates that calcium plays an important role in regulating protein trafficking and T-cell signalling, and the subsequent inflammatory gene expression infers an involvement of NFAT in CXCL8 regulation.Understanding these regulatory patterns provide clarification of conditions that involve altered intracellular signalling leading to T-cell-derived cytokine expression.

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