Rudajev Vladimir, Novotny Jiri
Department of Physiology, Faculty of Science, Charles University, Prague, Czechia.
Front Mol Neurosci. 2022 Aug 25;15:937056. doi: 10.3389/fnmol.2022.937056. eCollection 2022.
Alzheimer's disease (AD) is a neurodegenerative disorder that is one of the most devastating and widespread diseases worldwide, mainly affecting the aging population. One of the key factors contributing to AD-related neurotoxicity is the production and aggregation of amyloid β (Aβ). Many studies have shown the ability of Aβ to bind to the cell membrane and disrupt its structure, leading to cell death. Because amyloid damage affects different parts of the brain differently, it seems likely that not only Aβ but also the nature of the membrane interface with which the amyloid interacts, helps determine the final neurotoxic effect. Because cholesterol is the dominant component of the plasma membrane, it plays an important role in Aβ-induced toxicity. Elevated cholesterol levels and their regulation by statins have been shown to be important factors influencing the progression of neurodegeneration. However, data from many studies have shown that cholesterol has both neuroprotective and aggravating effects in relation to the development of AD. In this review, we attempt to summarize recent findings on the role of cholesterol in Aβ toxicity mediated by membrane binding in the pathogenesis of AD and to consider it in the broader context of the lipid composition of cell membranes.
阿尔茨海默病(AD)是一种神经退行性疾病,是全球最具破坏性和最为普遍的疾病之一,主要影响老年人群。导致AD相关神经毒性的关键因素之一是淀粉样β蛋白(Aβ)的产生和聚集。许多研究表明,Aβ能够与细胞膜结合并破坏其结构,从而导致细胞死亡。由于淀粉样蛋白损伤对大脑不同部位的影响不同,因此似乎不仅Aβ,而且淀粉样蛋白相互作用的膜界面的性质,都有助于确定最终的神经毒性作用。由于胆固醇是质膜的主要成分,它在Aβ诱导的毒性中起重要作用。胆固醇水平升高及其通过他汀类药物的调节已被证明是影响神经退行性变进展的重要因素。然而,许多研究的数据表明,胆固醇在AD的发展过程中既具有神经保护作用,也具有加重作用。在这篇综述中,我们试图总结胆固醇在AD发病机制中通过膜结合介导的Aβ毒性作用的最新研究发现,并在更广泛的细胞膜脂质组成背景下进行考虑。