Hojyo Shintaro, Fukada Toshiyuki
Deutsches Rheuma-Forschungszentrum, Berlin, Osteoimmunology, Berlin, Germany.
Faculty of Pharmaceutical Sciences, Tokushima Bunri University, Japan.
Arch Biochem Biophys. 2016 Dec 1;611:43-50. doi: 10.1016/j.abb.2016.06.020. Epub 2016 Jul 6.
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.
锌(Zn)是一种必需的微量元素,由于其对各种转录因子和酶的表达及活性有影响,在广泛的细胞机制中至关重要。锌缺乏会扰乱锌稳态,并产生致病后果,包括哺乳动物的生长迟缓及免疫功能受损。锌稳态由锌转运蛋白和金属硫蛋白的协同活性严格控制,它们调节锌的分布、储存以及细胞内和细胞外浓度。最近利用锌转运蛋白缺陷小鼠的反向遗传学方法揭示了特定锌信号轴(每个由锌和一个锌转运蛋白形成)在各种生物学程序中的生理功能。在本综述中,我们描述了关于锌转运蛋白作用的最新发现,这些转运蛋白通过在生理和发病机制中摄取锌来促进细胞信号传导,特别关注锌信号在全身生长和免疫中的影响。