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锌转运体及其在胰腺β细胞中的作用。

Zinc transporters and their role in the pancreatic β-cell.

作者信息

Lemaire Katleen, Chimienti Fabrice, Schuit Frans

机构信息

Gene Expression Unit, Department of Molecular Cell Biology, KU Leuven, Leuven, Belgium.

Mellitech, INAC/SCIB, CEA Grenoble, Grenoble, France.

出版信息

J Diabetes Investig. 2012 Jun 6;3(3):202-11. doi: 10.1111/j.2040-1124.2012.00199.x.

Abstract

Zinc is an essential nutrient with tremendous importance for human health, and zinc deficiency is a severe risk factor for increased mortality and morbidity. As abnormal zinc homeostasis causes diabetes, and because the pancreatic β-cell contains the highest zinc content of any known cell type, it is of interest to know how zinc fluxes are controlled in β-cells. The understanding of zinc homeostasis has been boosted by the discovery of multiprotein families of zinc transporters, and one of them - zinc transporter 8 (ZnT8) - is abundantly and specifically expressed in the pancreatic islets of Langerhans. In this review, we discuss the evidence for a physiological role of ZnT8 in the formation of zinc-insulin crystals, the physical form in which most insulin is stored in secretory granules. In addition, we cross-examine this information, collected in genetically modified mouse strains, to the knowledge that genetic variants of the human ZnT8 gene predispose to the onset of type 2 diabetes and that epitopes on the ZnT8 protein trigger autoimmunity in patients with type 1 diabetes. The overall conclusion is that we are still at the dawn of a complete understanding of how zinc homeostasis operates in normal β-cells and how abnormalities lead to β-cell dysfunction and diabetes. (J Diabetes Invest, doi: 10.1111/j.2040-1124.2012.00199.x, 2012).

摘要

锌是一种对人体健康极为重要的必需营养素,锌缺乏是导致死亡率和发病率上升的严重风险因素。由于锌稳态异常会引发糖尿病,且胰腺β细胞是所有已知细胞类型中锌含量最高的,因此了解β细胞中锌通量是如何被调控的很有意义。锌转运体多蛋白家族的发现推动了对锌稳态的认识,其中之一——锌转运体8(ZnT8)——在胰岛中大量且特异性表达。在这篇综述中,我们讨论了ZnT8在锌-胰岛素晶体形成过程中发挥生理作用的证据,胰岛素大多以这种物理形式储存在分泌颗粒中。此外,我们将在基因改造小鼠品系中收集到的这些信息,与人类ZnT8基因的遗传变异易引发2型糖尿病以及ZnT8蛋白上的表位会触发1型糖尿病患者自身免疫反应这一认知进行了对照研究。总体结论是,我们对于锌稳态在正常β细胞中如何发挥作用以及异常情况如何导致β细胞功能障碍和糖尿病的全面理解仍处于起步阶段。(《糖尿病研究杂志》,doi: 10.1111/j.2040 - 1124.2012.00199.x,2012年)

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df7a/4014939/5ed57ea6ff79/jdi-3-202-g1.jpg

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