通过Crtam调节T细胞极性和效应器功能的晚期阶段
Jung-Hua Yeh1, Sachdev S Sidhu, Andrew C Chan
1Department of Immunology, Genentech, Inc., 1 DNA Way, South San Francisco, CA 94080, USA.
Cell
|March 11, 2008
概括
第I类MHC受限制的T细胞相关分子 (Crtam) 建立了T细胞的晚期极性,增强了CD4+T细胞中的IFNgamma和IL22的产生. 这种动态调节会在初始激活数小时后影响自适应性免疫反应.
科学领域:
- 免疫学 免疫学 免疫学
- 细胞生物学 细胞生物学
- 分子生物学分子生物学
背景情况:
- 细胞蛋白组织对T细胞极性至关重要,影响细胞分裂,分化,迁移和器官生成.
- 抗原呈现细胞 (APC) 激活T细胞导致免疫突触 (IS) 的形成,涉及T细胞受体 (TCR) 信号传递,细胞骨变化,并在几个小时内产生第二个信使.
研究的目的:
- 调查Crtam在T细胞极性形成后期阶段的作用.
- 确定Crtam介导的晚极性对CD4+T细胞功能的功能影响.
主要方法:
- 演示Crtam与Scrib极性蛋白协调一个信号复合体.
- 对CD4+T细胞的分析:激活后6小时以上.
- 细胞因子产生的量化 (IFNgamma和IL22).
主要成果:
- 一种跨膜蛋白Crtam与Scrib结合了一个信号复合体,以在CD4+T细胞的一个子集中建立晚期T细胞极性.
- CD4+Crtam+ T细胞表现出选择性和增强的IFNgamma和IL22的产生.
- Crtam 参与影响了自适应性免疫反应,远远超出了最初的激活期.
结论:
- Crtam在建立T细胞极性晚期阶段中发挥着关键作用.
- 这种晚期的极性,由Crtam调解,增强了特定细胞因子的产生,从而调节了自适应性免疫反应.
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