酵母
内吞循环
毒性
有机体
疾病
淀粉样蛋白(真菌学)
模式生物
生物
阿尔茨海默病
医学
生物化学
遗传学
基因
细胞
病理
内科学
内吞作用
植物
作者
Sebastian Treusch,Shusei Hamamichi,Jessica L. Goodman,Kent Matlack,Chee Yeun Chung,Valeriya Baru,Joshua M. Shulman,Antonio Parrado,Brooke J. Bevis,Julie S. Valastyan,Haesun Han,Malin Lindhagen‐Persson,Eric M. Reiman,Denis A. Evans,David A. Bennett,Anders Olofsson,Philip L. DeJager,Rudolph E. Tanzi,Kim A. Caldwell,Guy A. Caldwell
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2011-10-27
卷期号:334 (6060): 1241-1245
被引量:380
标识
DOI:10.1126/science.1213210
摘要
Aβ (beta-amyloid peptide) is an important contributor to Alzheimer's disease (AD). We modeled Aβ toxicity in yeast by directing the peptide to the secretory pathway. A genome-wide screen for toxicity modifiers identified the yeast homolog of phosphatidylinositol binding clathrin assembly protein (PICALM) and other endocytic factors connected to AD whose relationship to Aβ was previously unknown. The factors identified in yeast modified Aβ toxicity in glutamatergic neurons of Caenorhabditis elegans and in primary rat cortical neurons. In yeast, Aβ impaired the endocytic trafficking of a plasma membrane receptor, which was ameliorated by endocytic pathway factors identified in the yeast screen. Thus, links between Aβ, endocytosis, and human AD risk factors can be ascertained with yeast as a model system.
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