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首页> 外文期刊>The Journal of Immunology: Official Journal of the American Association of Immunologists >Ca2+ signals in CD4+ T cells during early contacts with antigen-bearing dendritic cells in lymph node.
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Ca2+ signals in CD4+ T cells during early contacts with antigen-bearing dendritic cells in lymph node.

机译:在与淋巴结中带有抗原的树突状细胞早期接触的过程中,CD4 + T细胞中的Ca2 +信号。

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摘要

T cell activation by APC requires cytosolic Ca(2+) ([Ca(2+)](i)) elevation. Using two-photon microscopy, we visualized Ca(2+) signaling and motility of murine CD4(+) T cells within lymph node (LN) explants under control, inflammatory, and immunizing conditions. Without Ag under basal noninflammatory conditions, T cells showed infrequent Ca(2+) spikes associated with sustained slowing. Inflammation reduced velocities and Ca(2+) spiking in the absence of specific Ag. During early Ag encounter, most T cells engaged Ag-presenting dendritic cells in clusters, and showed increased Ca(2+) spike frequency and elevated basal [Ca(2+)](i). These Ca(2+) signals persisted for hours, irrespective of whether T cells were in contact with visualized dendritic cells. We propose that sustained increases in basal [Ca(2+)](i) and spiking frequency constitute a Ca(2+) signaling modality that, integrated over hours, distinguishes immunogenic from basal state in the native lymphoid environment.
机译:APC激活T细胞需要胞质Ca(2+)([Ca(2 +)](i))升高。使用双光子显微镜,我们可视化在控制,炎症和免疫条件下淋巴结(LN)外植体内的小鼠CD4(+)T细胞的Ca(2+)信号和运动。在基础非炎性条件下没有银,T细胞显示罕见的Ca(2+)峰值与持续减慢相关。炎症降低速度和Ca(2+)尖峰在没有特定Ag的情况下。在早期的Ag接触过程中,大多数T细胞与簇中呈递Ag的树突状细胞接合,并显示出增加的Ca(2+)尖峰频率和升高的基础[Ca(2 +)](i)。这些Ca(2+)信号持续数小时,无论T细胞是否与可见的树突状细胞接触。我们建议持续增加基础[Ca(2 +)](i)和尖峰频率构成Ca(2+)信号方式,经过数小时整合,将免疫原性与天然淋巴环境中的基础状态区分开。

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