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锌的关键作用:超越对心肌信号传导的影响

The Critical Roles of Zinc: Beyond Impact on Myocardial Signaling.

作者信息

Lee Sung Ryul, Noh Su Jin, Pronto Julius Ryan, Jeong Yu Jeong, Kim Hyoung Kyu, Song In Sung, Xu Zhelong, Kwon Hyog Young, Kang Se Chan, Sohn Eun-Hwa, Ko Kyung Soo, Rhee Byoung Doo, Kim Nari, Han Jin

机构信息

Department of Integrated Biomedical Science, Cardiovascular and Metabolic disease Center, College of Medicine, Inje University, Busan 614-735, Korea.

Department of Physiology, Graduate School of Inje University, Cardiovascular and Metabolic Disease Center, Inje University, Busan 614-735, Korea.

出版信息

Korean J Physiol Pharmacol. 2015 Sep;19(5):389-99. doi: 10.4196/kjpp.2015.19.5.389. Epub 2015 Aug 20.

Abstract

Zinc has been considered as a vital constituent of proteins, including enzymes. Mobile reactive zinc (Zn(2+)) is the key form of zinc involved in signal transductions, which are mainly driven by its binding to proteins or the release of zinc from proteins, possibly via a redox switch. There has been growing evidence of zinc's critical role in cell signaling, due to its flexible coordination geometry and rapid shifts in protein conformation to perform biological reactions. The importance and complexity of Zn(2+) activity has been presumed to parallel the degree of calcium's participation in cellular processes. Whole body and cellular Zn(2+) levels are largely regulated by metallothioneins (MTs), Zn(2+) importers (ZIPs), and Zn(2+) transporters (ZnTs). Numerous proteins involved in signaling pathways, mitochondrial metabolism, and ion channels that play a pivotal role in controlling cardiac contractility are common targets of Zn(2+). However, these regulatory actions of Zn(2+) are not limited to the function of the heart, but also extend to numerous other organ systems, such as the central nervous system, immune system, cardiovascular tissue, and secretory glands, such as the pancreas, prostate, and mammary glands. In this review, the regulation of cellular Zn(2+) levels, Zn(2+)-mediated signal transduction, impacts of Zn(2+) on ion channels and mitochondrial metabolism, and finally, the implications of Zn(2+) in health and disease development were outlined to help widen the current understanding of the versatile and complex roles of Zn(2+).

摘要

锌被认为是蛋白质(包括酶)的重要组成部分。可移动的活性锌(Zn(2+))是参与信号转导的关键锌形式,信号转导主要由其与蛋白质的结合或锌从蛋白质中的释放驱动,可能通过氧化还原开关实现。由于锌具有灵活的配位几何结构以及蛋白质构象的快速变化以进行生物反应,越来越多的证据表明锌在细胞信号传导中起关键作用。据推测,Zn(2+)活性的重要性和复杂性与钙参与细胞过程的程度相当。全身和细胞内的Zn(2+)水平在很大程度上受金属硫蛋白(MTs)、Zn(2+)进口蛋白(ZIPs)和Zn(2+)转运蛋白(ZnTs)的调节。参与信号通路、线粒体代谢和离子通道且在控制心脏收缩性中起关键作用的众多蛋白质是Zn(2+)的常见靶点。然而,Zn(2+)的这些调节作用不仅限于心脏功能,还扩展到许多其他器官系统,如中枢神经系统、免疫系统、心血管组织以及分泌腺,如胰腺、前列腺和乳腺。在本综述中,概述了细胞内Zn(2+)水平的调节、Zn(2+)介导的信号转导、Zn(2+)对离子通道和线粒体代谢的影响,以及最后Zn(2+)在健康和疾病发展中的意义,以帮助拓宽目前对Zn(2+)多样而复杂作用的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7142/4553398/00c425cc808d/kjpp-19-389-g001.jpg

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