Neilson J, Stankunas K, Crabtree G R
Department of Microbiology and Immunology, Stanford University Medical School, 279 Campus Drive, 94305, Stanford, CA, USA.
Curr Opin Immunol. 2001 Jun;13(3):346-50. doi: 10.1016/s0952-7915(00)00225-9.
Recent structural studies have supported a kinetic model of TCR activation, raising the question of how the duration of receptor occupancy is translated into activation of immune response genes. We summarize evidence that the cytoplasmic-to-nuclear shuttling of NF-ATc family members monitors the duration of receptor occupancy.
最近的结构研究支持了TCR激活的动力学模型,这就提出了一个问题,即受体占据的持续时间是如何转化为免疫反应基因的激活的。我们总结了证据表明NF-ATc家族成员的胞质到核穿梭监测受体占据的持续时间。