Gebert Magdalena, Sławski Jakub, Kalinowski Leszek, Collawn James F, Bartoszewski Rafal
Department of Medical Laboratory Diagnostics-Fahrenheit Biobank BBMRI.pl, Medical University of Gdansk, 80-134 Gdansk, Poland.
Department of Biophysics, Faculty of Biotechnology, University of Wroclaw, F. Joliot-Curie 14a Street, 50-383 Wroclaw, Poland.
Antioxidants (Basel). 2023 Aug 21;12(8):1648. doi: 10.3390/antiox12081648.
Efficient brain function requires as much as 20% of the total oxygen intake to support normal neuronal cell function. This level of oxygen usage, however, leads to the generation of free radicals, and thus can lead to oxidative stress and potentially to age-related cognitive decay and even neurodegenerative diseases. The regulation of this system requires a complex monitoring network to maintain proper oxygen homeostasis. Furthermore, the high content of mitochondria in the brain has elevated glucose demands, and thus requires a normal redox balance. Maintaining this is mediated by adaptive stress response pathways that permit cells to survive oxidative stress and to minimize cellular damage. These stress pathways rely on the proper function of the endoplasmic reticulum (ER) and the activation of the unfolded protein response (UPR), a cellular pathway responsible for normal ER function and cell survival. Interestingly, the UPR has two opposing signaling pathways, one that promotes cell survival and one that induces apoptosis. In this narrative review, we discuss the opposing roles of the UPR signaling pathways and how a better understanding of these stress pathways could potentially allow for the development of effective strategies to prevent age-related cognitive decay as well as treat neurodegenerative diseases.
高效的脑功能需要高达总氧气摄入量的20%来支持正常的神经元细胞功能。然而,这种氧气使用水平会导致自由基的产生,进而可能导致氧化应激,并有可能导致与年龄相关的认知衰退甚至神经退行性疾病。该系统的调节需要一个复杂的监测网络来维持适当的氧稳态。此外,大脑中线粒体含量高,对葡萄糖的需求增加,因此需要正常的氧化还原平衡。维持这一平衡是由适应性应激反应途径介导的,这些途径使细胞能够在氧化应激中存活并将细胞损伤降至最低。这些应激途径依赖于内质网(ER)的正常功能和未折叠蛋白反应(UPR)的激活,UPR是一种负责内质网正常功能和细胞存活的细胞途径。有趣的是,UPR有两个相反的信号通路,一个促进细胞存活,另一个诱导细胞凋亡。在这篇叙述性综述中,我们讨论了UPR信号通路的相反作用,以及更好地理解这些应激途径如何有可能开发出有效的策略来预防与年龄相关的认知衰退以及治疗神经退行性疾病。