Cardiff University, Dementia Research Institute, Cardiff University¸ Cardiff, CF24 4HQ, UK.
Philos Trans R Soc Lond B Biol Sci. 2024 Apr 8;379(1899):20220378. doi: 10.1098/rstb.2022.0378. Epub 2024 Feb 19.
Endocytosis is a key cellular pathway required for the internalization of cellular nutrients, lipids and receptor-bound cargoes. It is also critical for the recycling of cellular components, cellular trafficking and membrane dynamics. The endocytic pathway has been consistently implicated in Alzheimer's disease (AD) through repeated genome-wide association studies and the existence of rare coding mutations in endocytic genes. and are two of the most significant late-onset AD risk genes after and are both key to clathrin-mediated endocytic biology. Pathological studies also demonstrate that endocytic dysfunction is an early characteristic of late-onset AD, being seen in the prodromal phase of the disease. Different cell types of the brain have specific requirements of the endocytic pathway. Neurons require efficient recycling of synaptic vesicles and microglia use the specialized form of endocytosis-phagocytosis-for their normal function. Therefore, disease-associated changes in endocytic genes will have varied impacts across different cell types, which remains to be fully explored. Given the genetic and pathological evidence for endocytic dysfunction in AD, understanding how such changes and the related cell type-specific vulnerabilities impact normal cellular function and contribute to disease is vital and could present novel therapeutic opportunities. This article is part of a discussion meeting issue 'Understanding the endo-lysosomal network in neurodegeneration'.
内吞作用是细胞内化细胞营养物质、脂质和受体结合货物所必需的关键细胞途径。它对于细胞成分的再循环、细胞运输和膜动力学也至关重要。通过反复的全基因组关联研究和内吞作用基因中罕见编码突变的存在,内吞作用途径一直与阿尔茨海默病(AD)有关。 和 是除 之外最重要的两种晚发性 AD 风险基因,它们都是网格蛋白介导的内吞生物学的关键。病理研究还表明,内吞作用功能障碍是晚发性 AD 的早期特征,在疾病的前驱期就可见到。大脑的不同细胞类型对内吞作用途径有特定的要求。神经元需要有效地回收突触囊泡,而小胶质细胞则利用内吞作用的特殊形式——吞噬作用——来发挥其正常功能。因此,与疾病相关的内吞作用基因的变化将对不同的细胞类型产生不同的影响,这仍有待充分探索。鉴于 AD 中内吞作用功能障碍的遗传和病理证据,了解这些变化以及相关的细胞类型特异性脆弱性如何影响正常细胞功能并导致疾病是至关重要的,并且可能提供新的治疗机会。本文是关于“理解神经退行性疾病中的内体-溶酶体网络”的讨论会议的一部分。