van den Berg Hugo A, Rand David A
Interdisciplinary Programme for Cellular Regulation Mathematics Institute, University of Warwick, Coventry CV4 7AL, UK.
J Theor Biol. 2004 Jun 7;228(3):397-416. doi: 10.1016/j.jtbi.2004.02.002.
T lymphocytes are believed to alter their sensitivity to TCR stimulation by means of a tunable cellular activation threshold. We present two modelling examples which show that the concept of a tunable threshold can be made mechanistically plausible. The tunable threshold is treated as an emergent property of the dynamics of the T cell's signalling machinery. In addition, we discuss how the dynamic properties of activation threshold tuning can be determined experimentally with the aid of these two models. We propose a novel 'avidity selection' mechanism for the initial stages of the immune response, based on the properties of the T cell activation threshold tuning mechanism we propose for the commitment to differentiation. Our main finding is that activation threshold tuning allows T cells to respond to relevant ligands with a detection threshold that is (i) uniform across both the T cell repertoire and the secondary lymphoid tissues, while (ii) retaining tolerance to autostimulation. Our analysis indicates that central tolerance enhances the efficiency of peripheral tolerance, casting new light on the role of negative selection in the thymus.
人们认为T淋巴细胞通过可调的细胞激活阈值来改变其对TCR刺激的敏感性。我们给出了两个建模示例,表明可调阈值的概念在机制上是合理的。可调阈值被视为T细胞信号传导机制动力学的一种涌现特性。此外,我们讨论了如何借助这两个模型通过实验确定激活阈值调节的动态特性。基于我们提出的用于分化承诺的T细胞激活阈值调节机制的特性,我们为免疫反应的初始阶段提出了一种新的“亲和力选择”机制。我们的主要发现是,激活阈值调节使T细胞能够以一种检测阈值对相关配体做出反应,该检测阈值(i)在整个T细胞库和二级淋巴组织中是统一的,同时(ii)保持对自身刺激的耐受性。我们的分析表明,中枢耐受增强了外周耐受的效率,为胸腺中阴性选择的作用提供了新的视角。