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首页> 外文期刊>The Journal of Immunology: Official Journal of the American Association of Immunologists >A Pivotal Role for the Multifunctional Calcium/Calmodulin-Dependent Protein Kinase II in T Cells: From Activation to Unresponsiveness.
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A Pivotal Role for the Multifunctional Calcium/Calmodulin-Dependent Protein Kinase II in T Cells: From Activation to Unresponsiveness.

机译:多功能钙/钙调蛋白依赖性蛋白激酶II在T细胞中的关键作用:从激活到无反应性。

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摘要

Stimulation of the TCR leads to an oscillatory release of free calcium that activates members of the calcium/calmodulin-dependent protein kinase II (CaMKII) family. The CaMKII molecules have profound and lasting effects on cellular signaling in several cell types, yet the role of CaMKII in T cells is still poorly characterized. In this report we describe a splice variant of CaMKIIbeta, CaMKIIbeta'e, in mouse T cells. We have determined its function, along with that of CaMKIIgamma, by introducing the active and kinase-dead mutants into activated P14 TCR transgenic T cells using retroviral transduction. Active CaMKII enhanced the proliferation and cytotoxic activity of T cells while reducing their IL-2 production. Furthermore, it induced a profound state of unresponsiveness that could be overcome only by prolonged culture in IL-2. These results indicate that members of the CaMKII family play an important role in regulation of CD8 T cell proliferation, cytotoxic effector function, and the response to restimulation.
机译:TCR的刺激导致游离钙的振荡释放,从而激活钙/钙调蛋白依赖性蛋白激酶II(CaMKII)家族的成员。 CaMKII分子在几种细胞类型中对细胞信号传导具有深远而持久的影响,但CaMKII在T细胞中的作用仍不明确。在此报告中,我们描述了小鼠T细胞中CaMKIIbeta,CaMKIIbeta'e的剪接变体。我们已经确定了其功能,连同CaMKIIgamma,通过使用逆转录病毒转导将活性和激酶死亡突变体引入活化的P14 TCR转基因T细胞中。活性CaMKII增强T细胞的增殖和细胞毒性活性,同时降低其IL-2产生。此外,它诱导了无反应的深刻状态,只有在IL-2中长时间培养才能克服。这些结果表明,CaMKII家族的成员在调节CD8 T细胞增殖,细胞毒性效应子功能以及对再刺激的反应中起着重要作用。

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