Division of Immunology, Lowance Center for Human Immunology, Department of Medicine, Emory University School of Medicine, United States.
Division of Immunology, Lowance Center for Human Immunology, Department of Medicine, Emory University School of Medicine, United States.
Curr Opin Immunol. 2021 Dec;73:43-49. doi: 10.1016/j.coi.2021.09.007. Epub 2021 Oct 12.
Mature CD4 and CD8 T cells constitutively experience weak T cell receptor (TCR) stimulation in response to self-antigens, termed tonic (or basal) signaling. How tonic TCR signal strength impacts T cell responses to foreign antigens is an active area of investigation. Such studies rely on surrogate markers of tonic signal strength, including CD5, Ly6C, and transgenic reporters of Nr4a genes. Recent research indicates that strong tonic TCR signal strength influences basal T cell metabolism, effector differentiation, and TCR signal transduction. T cells that experience the strongest tonic TCR signaling exhibit features of T cell activation and negative regulation. These data suggest a model whereby adaptation to tonic signaling has lasting effects that alter T cell activation and differentiation.
成熟的 CD4 和 CD8 T 细胞持续受到自身抗原的弱 T 细胞受体 (TCR) 刺激,这种刺激被称为基础 (或基础) 信号。基础 TCR 信号强度如何影响 T 细胞对外来抗原的反应是一个活跃的研究领域。此类研究依赖于基础信号强度的替代标志物,包括 CD5、Ly6C 和 Nr4a 基因的转基因报告基因。最近的研究表明,强烈的基础 TCR 信号强度会影响基础 T 细胞代谢、效应细胞分化和 TCR 信号转导。经历最强基础 TCR 信号的 T 细胞表现出 T 细胞激活和负调节的特征。这些数据表明,适应基础信号具有持久的影响,改变 T 细胞的激活和分化。