St. Jude Children's Research Hospital, Department of Immunology, 262 Danny Thomas Place, Memphis, TN 38105, United States.
Semin Immunol. 2012 Dec;24(6):399-404. doi: 10.1016/j.smim.2012.12.006. Epub 2013 Jan 11.
As T cells respond to pathogens, they must transition from a quiescent, naïve state, to a rapidly proliferating, active effector state, and back again to a quiescent state as they develop into memory cells. Such transitions place unique metabolic demands on the differentiating cells. T cells meet these demands by altering their metabolic profiles, which are, in turn, regulated by distinct signaling cascades and transcriptional programs. Here, we examine the metabolic profiles of T cells during an acute immune response and discuss the signal and transcriptional regulators of these metabolic changes.
当 T 细胞对病原体作出反应时,它们必须从静止、幼稚的状态转变为快速增殖、活跃的效应状态,并在分化为记忆细胞后再次回到静止状态。这种转变对分化细胞提出了独特的代谢需求。T 细胞通过改变其代谢谱来满足这些需求,而代谢谱又受到不同信号级联和转录程序的调节。在这里,我们研究了急性免疫反应期间 T 细胞的代谢谱,并讨论了这些代谢变化的信号和转录调节因子。