Zhang Zhong-Hao, Song Guo-Li
Shenzhen Key Laboratory of Marine Bioresources and Ecology, College of Life Sciences and Oceanography, Shenzhen University, Shenzhen, China.
Shenzhen Bay Laboratory, Shenzhen, China.
Front Neurosci. 2021 Mar 8;15:646518. doi: 10.3389/fnins.2021.646518. eCollection 2021.
Selenium (Se) and its compounds have been reported to have great potential in the prevention and treatment of Alzheimer's disease (AD). However, little is known about the functional mechanism of Se in these processes, limiting its further clinical application. Se exerts its biological functions mainly through selenoproteins, which play vital roles in maintaining optimal brain function. Therefore, selenoproteins, especially brain function-associated selenoproteins, may be involved in the pathogenesis of AD. Here, we analyze the expression and distribution of 25 selenoproteins in the brain and summarize the relationships between selenoproteins and brain function by reviewing recent literature and information contained in relevant databases to identify selenoproteins (GPX4, SELENOP, SELENOK, SELENOT, GPX1, SELENOM, SELENOS, and SELENOW) that are highly expressed specifically in AD-related brain regions and closely associated with brain function. Finally, the potential functions of these selenoproteins in AD are discussed, for example, the function of GPX4 in ferroptosis and the effects of the endoplasmic reticulum (ER)-resident protein SELENOK on Ca homeostasis and receptor-mediated synaptic functions. This review discusses selenoproteins that are closely associated with brain function and the relevant pathways of their involvement in AD pathology to provide new directions for research on the mechanism of Se in AD.
据报道,硒(Se)及其化合物在预防和治疗阿尔茨海默病(AD)方面具有巨大潜力。然而,人们对硒在这些过程中的功能机制了解甚少,这限制了其进一步的临床应用。硒主要通过硒蛋白发挥其生物学功能,而硒蛋白在维持最佳脑功能方面起着至关重要的作用。因此,硒蛋白,尤其是与脑功能相关的硒蛋白,可能参与了AD的发病机制。在此,我们通过回顾近期文献及相关数据库中的信息,分析了25种硒蛋白在脑中的表达和分布,并总结了硒蛋白与脑功能之间的关系,以确定在AD相关脑区中特异性高表达且与脑功能密切相关的硒蛋白(谷胱甘肽过氧化物酶4(GPX4)、硒蛋白P(SELENOP)、硒蛋白K(SELENOK)、硒蛋白T(SELENOT)、谷胱甘肽过氧化物酶1(GPX1)、硒蛋白M(SELENOM)、硒蛋白S(SELENOS)和硒蛋白W(SELENOW))。最后,讨论了这些硒蛋白在AD中的潜在功能,例如,GPX4在铁死亡中的功能以及内质网驻留蛋白SELENOK对钙稳态和受体介导的突触功能的影响。本综述讨论了与脑功能密切相关的硒蛋白及其参与AD病理的相关途径,为研究硒在AD中的作用机制提供新的方向。