Laboratory of Immune Regulation, Graduate School of Pharmaceutical Sciences, Suzuka University of Medical Science, 3500-3 Minamitamagaki, Suzuka, Mie 513-8607, Japan.
Laboratory of Immune Regulation, Faculty of Pharmaceutical Sciences, Suzuka University of Medical Science, 3500-3 Minamitamagaki-cho, Suzuka, Mie 513-8670, Japan.
J Immunol Res. 2018 Nov 25;2018:5749120. doi: 10.1155/2018/5749120. eCollection 2018.
Zinc is essential for maintaining normal structure and physiological function of cells. Its deficiency causes growth retardation, immunodeficiency, and neuronal degeneration. Zinc homeostasis is tightly regulated by zinc transporters and metallothioneins that control zinc concentration and its distribution in individual cells and contributes to zinc signaling. The intracellular zinc signaling regulates immune reactions. Although many molecules involved in these processes have zinc-binding motifs, the molecular mechanisms and the role of zinc in immune responses have not been elucidated. We and others have demonstrated that zinc signaling plays diverse and specific roles and in studies using knockout mice lacking zinc transporter function and metallothionein function. In this review, we discuss the impact of zinc signaling focusing particularly on mast cell-, basophil-, and T cell-mediated inflammatory and allergic responses. We also describe zinc signaling dysregulation as a leading health problem in inflammatory disease and allergy.
锌对于维持细胞的正常结构和生理功能是必需的。其缺乏会导致生长迟缓、免疫缺陷和神经元变性。锌稳态由锌转运体和金属硫蛋白严格调控,它们控制着细胞内锌的浓度及其分布,并有助于锌信号转导。细胞内锌信号转导调节免疫反应。虽然许多参与这些过程的分子都具有锌结合基序,但锌在免疫反应中的分子机制和作用尚未阐明。我们和其他人已经证明,锌信号转导在使用缺乏锌转运体功能和金属硫蛋白功能的敲除小鼠的研究中发挥了多样化和特定的作用。在这篇综述中,我们讨论了锌信号转导的影响,特别是聚焦于肥大细胞、嗜碱性粒细胞和 T 细胞介导的炎症和过敏反应。我们还描述了锌信号转导失调作为炎症性疾病和过敏的一个主要健康问题。