Masters Thomas A, Tumbarello David A, Chibalina Margarita V, Buss Folma
Cambridge Institute for Medical Research, Wellcome Trust/MRC Building, Hills Road, Cambridge CB2 0XY, UK.
Cambridge Institute for Medical Research, Wellcome Trust/MRC Building, Hills Road, Cambridge CB2 0XY, UK.
Cell Rep. 2017 Jun 6;19(10):2088-2101. doi: 10.1016/j.celrep.2017.05.048.
APPL1- and RAB5-positive signaling endosomes play a crucial role in the activation of AKT in response to extracellular stimuli. Myosin VI (MYO6) and two of its cargo adaptor proteins, GIPC and TOM1/TOM1L2, localize to these peripheral endosomes and mediate endosome association with cortical actin filaments. Loss of MYO6 leads to the displacement of these endosomes from the cell cortex and accumulation in the perinuclear space. Depletion of this myosin not only affects endosome positioning, but also induces actin and lipid remodeling consistent with endosome maturation, including accumulation of F-actin and the endosomal lipid PI(3)P. These processes acutely perturb endosome function, as both AKT phosphorylation and RAC-dependent membrane ruffling were markedly reduced by depletion of either APPL1 or MYO6. These results place MYO6 and its binding partners at a central nexus in cellular signaling linking actin dynamics at the cell surface and endosomal signaling in the cell cortex.
APPL1和RAB5阳性的信号内体在响应细胞外刺激时对AKT的激活起着关键作用。肌球蛋白VI(MYO6)及其两个货物衔接蛋白GIPC和TOM1/TOM1L2定位于这些外周内体,并介导内体与皮质肌动蛋白丝的结合。MYO6的缺失导致这些内体从细胞皮质移位并积聚在核周空间。这种肌球蛋白的缺失不仅影响内体定位,还诱导与内体成熟一致的肌动蛋白和脂质重塑,包括F-肌动蛋白和内体脂质PI(3)P的积累。这些过程严重扰乱内体功能,因为APPL1或MYO6的缺失均显著降低了AKT磷酸化和RAC依赖性膜皱褶。这些结果表明,MYO6及其结合伙伴在连接细胞表面肌动蛋白动力学和细胞皮质内体信号的细胞信号传导中处于核心枢纽位置。