Long Eric O
Laboratory of Immunogenetics, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, MD 20852, USA.
Immunol Rev. 2008 Aug;224:70-84. doi: 10.1111/j.1600-065X.2008.00660.x.
Receptors carrying immunoreceptor tyrosine-based inhibition motifs (ITIMs) in their cytoplasmic tail control a vast array of cellular responses, ranging from autoimmunity, allergy, phagocytosis of red blood cells, graft versus host disease, to even neuronal plasticity in the brain. The inhibitory function of many receptors has been deduced on the basis of cytoplasmic ITIM sequences. Tight regulation of natural killer (NK) cell cytotoxicity and cytokine production by inhibitory receptors specific for major histocompatibility complex class I molecules has served as a model system to study the negative signaling pathway triggered by an ITIM-containing receptor in the physiological context of NK-target cell interactions. Advances in our understanding of the molecular details of inhibitory signaling in NK cells have provided a conceptual framework to address how ITIM-mediated regulation controls cellular reactivity in diverse cell types.
其胞质尾部携带基于免疫受体酪氨酸抑制基序(ITIM)的受体控制着大量细胞反应,范围从自身免疫、过敏、红细胞吞噬作用、移植物抗宿主病,甚至到大脑中的神经元可塑性。许多受体的抑制功能是根据胞质ITIM序列推导出来的。主要组织相容性复合体I类分子特异性抑制性受体对自然杀伤(NK)细胞细胞毒性和细胞因子产生的严格调控,已成为在NK靶细胞相互作用的生理背景下研究含ITIM受体触发的负向信号通路的模型系统。我们对NK细胞中抑制性信号分子细节理解的进展,为解决ITIM介导的调控如何控制不同细胞类型中的细胞反应性提供了一个概念框架。