Jeon Yu-Mi, Kwon Younghwi, Lee Shinrye, Kim Hyung-Jun
Dementia Research Group, Korea Brain Research Institute, Daegu, Republic of Korea.
Department of Brain and Cognitive Sciences, Daegu Gyeongbuk Institute of Science and Technology (DGIST), Daegu, Republic of Korea.
Front Aging Neurosci. 2023 Feb 15;15:1047897. doi: 10.3389/fnagi.2023.1047897. eCollection 2023.
The endoplasmic reticulum (ER) is a major organelle involved in protein quality control and cellular homeostasis. ER stress results from structural and functional dysfunction of the organelle, along with the accumulation of misfolded proteins and changes in calcium homeostasis, it leads to ER stress response pathway such as unfolded protein response (UPR). Neurons are particularly sensitive to the accumulation of misfolded proteins. Thus, the ER stress is involved in neurodegenerative diseases such as Alzheimer's disease, Parkinson's disease, prion disease and motor neuron disease (MND). Recently, the complex involvement of ER stress pathways has been demonstrated in experimental models of amyotrophic lateral sclerosis (ALS)/MND using pharmacological and genetic manipulation of the unfolded protein response (UPR), an adaptive response to ER stress. Here, we aim to provide recent evidence demonstrating that the ER stress pathway is an essential pathological mechanism of ALS. In addition, we also provide therapeutic strategies that can help treat diseases by targeting the ER stress pathway.
内质网(ER)是参与蛋白质质量控制和细胞稳态的主要细胞器。内质网应激源于该细胞器的结构和功能障碍,以及错误折叠蛋白质的积累和钙稳态的变化,它会引发内质网应激反应途径,如未折叠蛋白反应(UPR)。神经元对错误折叠蛋白质的积累特别敏感。因此,内质网应激与神经退行性疾病有关,如阿尔茨海默病、帕金森病、朊病毒病和运动神经元病(MND)。最近,利用未折叠蛋白反应(UPR)的药理学和基因操作,在内侧肌萎缩性侧索硬化症(ALS)/MND的实验模型中证明了内质网应激途径的复杂参与,未折叠蛋白反应是对内质网应激的一种适应性反应。在这里,我们旨在提供最新证据,证明内质网应激途径是ALS的一种重要病理机制。此外,我们还提供了可以通过靶向内质网应激途径来帮助治疗疾病的治疗策略。