Cai Zhi-You, Xiao Ming, Quazi Sohel H, Ke Zun-Yu
Department of Neurology, Chongqing General Hospital, Chongqing, China.
Department of Anatomy, Nanjing Medical University, Nanjing, Jiangsu Province, China.
Neural Regen Res. 2018 May;13(5):930-935. doi: 10.4103/1673-5374.232490.
Extracellular exosomes are formed inside the cytoplasm of cells in compartments known as multivesicular bodies. Thus, exosomes contain cytoplasmic content. Multivesicular bodies fuse with the plasma membrane and release exosomes into the extracellular environment. Comprehensive research suggests that exosomes act as both inflammatory intermediaries and critical inducers of oxidative stress to drive progression of Alzheimer's disease. An important role of exosomes in Alzheimer's disease includes the formation of neurofibrillary tangles and beta-amyloid production, clearance, and accumulation. In addition, exosomes are involved in neuroinflammation and oxidative stress, which both act as triggers for beta-amyloid pathogenesis and tau hyperphosphorylation. Further, it has been shown that exosomes are strongly associated with beta-amyloid clearance. Thus, effective measures for regulating exosome metabolism may be novel drug targets for Alzheimer's disease.
细胞外囊泡在称为多囊泡体的细胞内区室中于细胞质内形成。因此,囊泡包含细胞质成分。多囊泡体与质膜融合并将囊泡释放到细胞外环境中。综合研究表明,囊泡既是炎症介质又是氧化应激的关键诱导物,可推动阿尔茨海默病的进展。囊泡在阿尔茨海默病中的一个重要作用包括神经原纤维缠结的形成以及β淀粉样蛋白的产生、清除和积累。此外,囊泡参与神经炎症和氧化应激,这两者均作为β淀粉样蛋白发病机制和tau蛋白过度磷酸化的触发因素。此外,已表明囊泡与β淀粉样蛋白清除密切相关。因此,调节囊泡代谢的有效措施可能是阿尔茨海默病的新型药物靶点。