Zinc transporters and signaling in physiology and pathogenesis

被引:64
|
作者
Hojyo, Shintaro [1 ]
Fukada, Toshiyuki [2 ]
机构
[1] Deutsch Rheuma Forschungszentrum, Osteoimmunol, Berlin, Germany
[2] Tokushima Bunri Univ, Fac Pharmaceut Sci, Tokushima, Japan
基金
日本学术振兴会;
关键词
Zinc transporter; Signaling; Growth; Bone; Connective tissue; Immunity; EHLERS-DANLOS-SYNDROME; ACRODERMATITIS-ENTEROPATHICA; MEDIATED INHIBITION; GLUCOSE-HOMEOSTASIS; MICE LACKING; GENE; MUTATIONS; DEFICIENCY; RECEPTOR; EXPRESSION;
D O I
10.1016/j.abb.2016.06.020
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Zinc (Zn) is an essential trace element that is vital in a wide range of cellular machineries because of its effect on the expression and activity of various transcription factors and enzymes. Zn deficiency disturbs Zn homeostasis and has pathogenic consequences, including growth retardation and immune impairment in mammals. Zn homeostasis is tightly controlled by the coordinated activity of Zn transporters and metallothioneins, which regulate the distribution, storage, and intracellular and extracellular concentration of Zn. Recent reverse-genetic approaches using Zn transporter deficient mice have revealed the physiological functions of specific Zn signaling axes (each formed by Zn and a Zn transporter) in various biological programs. In this review, we describe recent discoveries about the role of Zn transporters which facilitate cellular signaling through Zn uptake in physiology and pathogenesis, with particular focus on the influence of Zn signaling in systemic growth and immunity. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:43 / 50
页数:8
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