Département des Sciences Biologiques, Université du Québec à Montréal, 141 Avenue du Président-Kennedy, Montréal, QC H2X 3X8, Canada.
Centre d'Excellence en Recherche sur les Maladies Orphelines-Fondation Courtois, Pavillon des Sciences biologiques, 141 Avenue du Président-Kennedy, Montréal, QC H2X 3Y7, Canada.
Int J Mol Sci. 2023 Jan 19;24(3):1971. doi: 10.3390/ijms24031971.
For the past several years, fundamental research on Sigma-1R (S1R) protein has unveiled its necessity for maintaining proper cellular homeostasis through modulation of calcium and lipid exchange between the endoplasmic reticulum (ER) and mitochondria, ER-stress response, and many other mechanisms. Most of these processes, such as ER-stress response and autophagy, have been associated with neuroprotective roles. In fact, improving these mechanisms using S1R agonists was beneficial in several brain disorders including neurodegenerative diseases. In this review, we will examine S1R subcellular localization and describe S1R-associated biological activity within these specific compartments, i.e., the Mitochondrion-Associated ER Membrane (MAM), ER-Lipid Droplet (ER-LD) interface, ER-Plasma Membreane (ER-PM) interface, and the Nuclear Envelope (NE). We also discussed how the dysregulation of these pathways contributes to neurodegenerative diseases, while highlighting the cellular mechanisms and key binding partners engaged in these processes.
在过去的几年中,对 Sigma-1R(S1R)蛋白的基础研究揭示了其通过调节内质网(ER)和线粒体之间的钙和脂质交换、内质网应激反应和许多其他机制来维持适当的细胞内稳态的必要性。这些过程中的大多数,如内质网应激反应和自噬,都与神经保护作用有关。事实上,使用 S1R 激动剂改善这些机制在包括神经退行性疾病在内的几种脑疾病中是有益的。在这篇综述中,我们将检查 S1R 的亚细胞定位,并描述 S1R 在内质网相关生物活性在这些特定区域中的作用,即线粒体相关内质网膜(MAM)、内质网脂滴(ER-LD)界面、内质网-质膜(ER-PM)界面和核膜(NE)。我们还讨论了这些途径的失调如何导致神经退行性疾病,同时强调了参与这些过程的细胞机制和关键结合伙伴。