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锌离子载体吡啶硫酮在CD3激活的T细胞中模拟CD28共刺激信号。

Zinc Ionophore Pyrithione Mimics CD28 Costimulatory Signal in CD3 Activated T Cells.

作者信息

Jakobs Jana, Rink Lothar

机构信息

Institute of Immunology, Faculty of Medicine, RWTH Aachen University, Pauwelsstraße 30, 52074 Aachen, Germany.

出版信息

Int J Mol Sci. 2024 Apr 12;25(8):4302. doi: 10.3390/ijms25084302.

Abstract

Zinc is an essential trace element that plays a crucial role in T cell immunity. During T cell activation, zinc is not only structurally important, but zinc signals can also act as a second messenger. This research investigates zinc signals in T cell activation and their function in T helper cell 1 differentiation. For this purpose, peripheral blood mononuclear cells were activated via the T cell receptor-CD3 complex, and via CD28 as a costimulatory signal. Fast and long-term changes in intracellular zinc and calcium were monitored by flow cytometry. Further, interferon (IFN)-γ was analyzed to investigate the differentiation into T helper 1 cells. We show that fast zinc fluxes are induced via CD3. Also, the intracellular zinc concentration dramatically increases 72 h after anti-CD3 and anti-CD28 stimulation, which goes along with the high release of IFN-γ. Interestingly, we found that zinc signals can function as a costimulatory signal for T helper cell 1 differentiation when T cells are activated only via CD3. These results demonstrate the importance of zinc signaling alongside calcium signaling in T cell differentiation.

摘要

锌是一种必需的微量元素,在T细胞免疫中发挥着关键作用。在T细胞活化过程中,锌不仅在结构上很重要,而且锌信号还可以作为第二信使。本研究调查了T细胞活化中的锌信号及其在辅助性T细胞1分化中的作用。为此,通过T细胞受体-CD3复合物以及作为共刺激信号的CD28激活外周血单核细胞。通过流式细胞术监测细胞内锌和钙的快速和长期变化。此外,分析干扰素(IFN)-γ以研究向辅助性T细胞1的分化。我们发现通过CD3可诱导快速的锌通量。同样,抗CD3和抗CD28刺激72小时后细胞内锌浓度显著增加,这与IFN-γ的高释放同时发生。有趣的是,我们发现当T细胞仅通过CD3激活时,锌信号可作为辅助性T细胞1分化的共刺激信号。这些结果证明了锌信号与钙信号在T细胞分化中的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2fc/11050009/be87138847ea/ijms-25-04302-g001.jpg

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