Cambridge Institute for Medical Research, Cambridge Biomedical Campus, University of Cambridge, Wellcome Trust/MRC Building, Hills Road, Cambridge, CB2 0XY, UK.
Cell Mol Life Sci. 2018 Jul;75(14):2613-2625. doi: 10.1007/s00018-018-2752-9. Epub 2018 Jan 24.
The processing of amyloid precursor protein (APP) to the neurotoxic pro-aggregatory Aβ peptide is controlled by the mechanisms that govern the trafficking and localisation of APP. We hypothesised that genes involved in endosomal protein sorting could play an important role in regulating APP processing and, therefore, analysed ~ 40 novel endosome-to-Golgi retrieval genes previously identified in a genome-wide siRNA screen. We report that phospholipase D3 (PLD3), a type II membrane protein, functions in endosomal protein sorting and plays an important role in regulating APP processing. PLD3 co-localises with APP in endosomes and loss of PLD3 function results in reduced endosomal tubules, impaired trafficking of several membrane proteins and reduced association of sortilin-like 1 with APP.
淀粉样前体蛋白(APP)向神经毒性聚集 Aβ肽的加工受到控制其运输和定位的机制控制。我们假设参与内体蛋白分选的基因可能在调节 APP 加工中发挥重要作用,因此,我们分析了之前在全基因组 siRNA 筛选中鉴定的~40 种新型内体到高尔基体回收基因。我们报告说,II 型膜蛋白磷脂酶 D3(PLD3)在内体蛋白分选中起作用,并在调节 APP 加工中起重要作用。PLD3 与 APP 在内涵体中共定位,PLD3 功能丧失导致内涵体小管减少,几种膜蛋白的运输受损,以及分选连接蛋白 1 与 APP 的结合减少。