Lu Yue, Abdullah Mohammad, Healy Liam R, Tambini Marc D
Department of Pharmacology, Physiology & Neuroscience New Jersey Medical School, Brain Health Institute, Rutgers, The State University of New Jersey, 185 South Orange Ave, Newark, NJ, 07103, USA.
bioRxiv. 2025 Jan 22:2025.01.20.633888. doi: 10.1101/2025.01.20.633888.
The Amyloid Precursor Protein (APP), a genetic cause of Alzheimer's disease (AD), is a type-I transmembrane protein that is metabolized by proteolysis in the endolysomal system. APP and its metabolites are secreted by cells in extracellular vesicles (EVs). To study the function of APP-containing EVs, we isolated App-EVs from rat primary neuronal conditioned media and proteomic analysis identified the Valosin-containing protein (Vcp) as molecular cargo. Pharmacological modulation of Vcp activity was found to alter App processing and global EV secretion in rat primary neurons. AD-associated knock-in mutations were found to alter the abundance of App-EVs and the trafficking of App metabolites within App-EVs, in a manner related to the epitopes generated by the nonamyloidogenic processing of App. The presence of Vcp suggests a role for App-EVs in the clearance of protein aggregates.
淀粉样前体蛋白(APP)是阿尔茨海默病(AD)的一个遗传病因,它是一种I型跨膜蛋白,在内溶酶体系统中通过蛋白水解作用进行代谢。APP及其代谢产物由细胞分泌到细胞外囊泡(EVs)中。为了研究含APP的EVs的功能,我们从大鼠原代神经元条件培养基中分离出App-EVs,蛋白质组学分析确定含缬酪肽蛋白(Vcp)为分子货物。发现对Vcp活性进行药理学调节可改变大鼠原代神经元中App的加工过程和整体EV分泌。发现与AD相关的敲入突变会改变App-EVs的丰度以及App-EVs内App代谢产物的运输,其方式与App非淀粉样生成加工产生的表位有关。Vcp的存在表明App-EVs在蛋白质聚集体清除中发挥作用。