Role of Zinc Signaling in the Regulation of Mast Cell-, Basophil-, and T Cell-Mediated Allergic Responses

被引:14
作者
Nishida, Keigo [1 ,2 ]
Uchida, Ryota [1 ]
机构
[1] Suzuka Univ Med Sci, Grad Sch Pharmaceut Sci, Lab Immune Regulat, 3500-3 Minamitamagaki, Suzuka, Mie 5138607, Japan
[2] Suzuka Univ Med Sci, Fac Pharmaceut Sci, Lab Immune Regulat, 3500-3 Minamitamagaki Cho, Suzuka, Mie 5138607, Japan
关键词
PROTEIN-KINASE-C; SODIUM-INDUCED COLITIS; KAPPA-B ACTIVATION; MESSENGER-RNA; ALKALINE-PHOSPHATASES; CALCINEURIN ACTIVITY; AIRWAY INFLAMMATION; BONE-MARROW; LABILE ZINC; ORAL ZINC;
D O I
10.1155/2018/5749120
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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 in vivo and in vitro 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.
引用
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页数:9
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