Klein Marcel, Hermey Guido
Institute for Molecular and Cellular Cognition, Center for Molecular Neurobiology Hamburg, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Neural Regen Res. 2023 Jul;18(7):1463-1471. doi: 10.4103/1673-5374.361544.
Evidence from genetics and from analyzing cellular and animal models have converged to suggest links between neurodegenerative disorders of early and late life. Here, we summarize emerging links between the most common late life neurodegenerative disease, Alzheimer's disease, and the most common early life neurodegenerative diseases, neuronal ceroid lipofuscinoses. Genetic studies reported an overlap of clinically diagnosed Alzheimer's disease and mutations in genes known to cause neuronal ceroid lipofuscinoses. Accumulating data strongly suggest dysfunction of intracellular trafficking mechanisms and the autophagy-endolysosome system in both types of neurodegenerative disorders. This suggests shared cytopathological processes underlying these different types of neurodegenerative diseases. A better understanding of the common mechanisms underlying the different diseases is important as this might lead to the identification of novel targets for therapeutic concepts, the transfer of therapeutic strategies from one disease to the other and therapeutic approaches tailored to patients with specific mutations. Here, we review dysfunctions of the endolysosomal autophagy pathway in Alzheimer's disease and neuronal ceroid lipofuscinoses and summarize emerging etiologic and genetic overlaps.
遗传学以及对细胞和动物模型的分析证据都表明,早发性和晚发性神经退行性疾病之间存在联系。在此,我们总结了最常见的晚发性神经退行性疾病——阿尔茨海默病,与最常见的早发性神经退行性疾病——神经元蜡样脂褐质沉积症之间新出现的联系。遗传学研究报告称,临床诊断的阿尔茨海默病与已知会导致神经元蜡样脂褐质沉积症的基因突变存在重叠。越来越多的数据有力地表明,这两种神经退行性疾病中细胞内运输机制和自噬 - 内溶酶体系统均存在功能障碍。这表明这些不同类型的神经退行性疾病存在共同的细胞病理学过程。更好地理解不同疾病背后的共同机制很重要,因为这可能会促成新型治疗靶点的识别、治疗策略从一种疾病向另一种疾病的转移,以及针对具有特定突变患者的个性化治疗方法。在此,我们综述了阿尔茨海默病和神经元蜡样脂褐质沉积症中内溶酶体自噬途径的功能障碍,并总结新出现的病因学和遗传学重叠情况。