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阿尔茨海默病相关膜蛋白的运输及其在疾病发病机制中的作用。

Trafficking of Alzheimer's disease-related membrane proteins and its participation in disease pathogenesis.

作者信息

Suzuki Toshiharu, Araki Yoichi, Yamamoto Tohru, Nakaya Tadashi

机构信息

Graduate School of Pharmaceutical Sciences, Hokkaido University, Kita 12-Nishi 6, Kita-ku, Sapporo 060-0812.

出版信息

J Biochem. 2006 Jun;139(6):949-55. doi: 10.1093/jb/mvj121.

Abstract

Alzheimer's disease (AD) is a common neurodegenerative disorder that causes senile dementia. The pathological characteristics are the appearance of neurofibrillary tangles comprising abnormally phosphorylated tau and senile plaques composed of amyloid beta-protein depositions. Amyloid beta-protein precursor (APP) and presenilin (PS) are known to be causative genes of familial AD. Recent analyses have documented that APP functions in the axonal transport of vesicles and PS regulates intracellular protein trafficking. Dystrophic neurites, in which APP and Alcadein accumulate in swollen axons, are also observed in AD brain. These pathological characteristics and the features of AD-related proteins suggest that AD is a disease of the vesicular transport system. Here we review recent progress of research on AD pathogenesis from the viewpoint of membrane trafficking.

摘要

阿尔茨海默病(AD)是一种常见的神经退行性疾病,可导致老年痴呆症。其病理特征是出现由异常磷酸化的tau组成的神经原纤维缠结以及由淀粉样β蛋白沉积形成的老年斑。已知淀粉样β蛋白前体(APP)和早老素(PS)是家族性AD的致病基因。最近的分析表明,APP在囊泡的轴突运输中发挥作用,而PS调节细胞内蛋白质运输。在AD大脑中还观察到营养不良性神经突,其中APP和阿尔卡德因积聚在肿胀的轴突中。这些病理特征以及AD相关蛋白的特性表明,AD是一种囊泡运输系统疾病。在此,我们从膜运输的角度综述AD发病机制的最新研究进展。

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