首页> 外文期刊>Clinical and Experimental Immunology: An Official Journal of the British Society for Immunology >Intracellular calcium signalling patterns reflect the differentiation status of human T cells.
【24h】

Intracellular calcium signalling patterns reflect the differentiation status of human T cells.

机译:细胞内钙信号传导模式反映了人类T细胞的分化状态。

获取原文
获取原文并翻译 | 示例
       

摘要

Stimulation of T lymphocytes results in the calcium-dependent activation and repression of a large number of genes. However, the functional response made by different T cell subsets is heterogeneous, as their differentiation results in alterations in their sensitivity to activation and in the secretion of cytokines. Here we have investigated the patterns of calcium responses in CD4 and CD8 T cell subsets to help explain their different responses to activation. CD4(+) CD45RA(+) T cells isolated freshly from human blood gave a sustained calcium signal after stimulation, but this was smaller than elicited in CD4(+) CD45RO(+) cells. On in vitro differentiation of CD4(+) CD45RA(+) cells to CD45RO(+), the level of the cytoplasmic calcium response rose initially, but then declined steadily during further rounds of differentiation. The proportion producing an oscillatory calcium response or not responding was increased and differentiation was accompanied by a shift in the calcium between intracellular pools. CD8(+) T cells gave a smaller calcium response than paired CD4(+) T cells and showed a difference in the numbers of cells giving a transient, rather than sustained, calcium signal. The increase in oscillating cells in the CD4(+) CD45RO(+) population may reflect the heterogeneity of this population, particularly in terms of cytokine production. The changing patterns of calcium responses in T cells as they differentiate may explain variation in the cellular response to activation at different stages in their lifespan and emphasize the importance of the both the quantity and the quality of the calcium signal in determining the outcome of T cell activation.
机译:T淋巴细胞的刺激导致大量基因的钙依赖性激活和抑制。然而,由不同的T细胞亚群产生的功能反应是异质的,因为它们的分化导致它们对活化的敏感性和细胞因子的分泌发生改变。在这里,我们研究了CD4和CD8 T细胞亚群中钙反应的模式,以帮助解释它们对激活的不同反应。从人血中新鲜分离得到的CD4(+)CD45RA(+)T细胞在刺激后产生了持续的钙信号,但是比CD4(+)CD45RO(+)细胞引起的钙信号小。在CD4(+)CD45RA(+)细胞体外分化为CD45RO(+)时,细胞质钙反应的水平最初上升,但随后在进一步的分化过程中稳定下降。产生振荡性钙反应或不反应的比例增加,并且分化伴随着细胞内池之间钙的移动。与配对的CD4(+)T细胞相比,CD8(+)T细胞的钙反应更小,并且显示出瞬时而不是持续的钙信号的细胞数量也有所不同。 CD4(+)CD45RO(+)群体中振荡细胞的增加可能反映了该群体的异质性,特别是在细胞因子产生方面。 T细胞分化时钙反应模式的变化可能解释了细胞响应在其生命的不同阶段活化的变化,并强调了钙信号的数量和质量在确定T细胞结局中的重要性激活。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号