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Rabin8 regulates neurite outgrowth in both GEF activity-dependent and -independent manners

机译:Rabin8以GEF活性依赖性和非依赖性方式调节神经突生长

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Many aspects of membrane-trafficking events are regulated by Rab-family small GTPases. Neurite outgrowth requires massive addition of proteins and lipids to the tips of growing neurites by membrane trafficking, and although several Rabs, including Rab8, Rab10, and Rab11, have been implicated in this process, their regulatory mechanisms during neurite outgrowth are poorly understood. Here, we show that Rabin8, a Rab8-guanine nucleotide exchange factor (GEF), regulates nerve growth factor (NGF)-induced neurite outgrowth of PC12 cells. Knockdown of Rabin8 results in inhibition of neurite outgrowth, whereas overexpression promotes it. We also find that Rab10 is a novel substrate of Rabin8 and that both Rab8 and Rab10 function during neurite outgrowth downstream of Rabin8. Surprisingly, however, a GEF activity-deficient isoform of Rabin8 also promotes neurite outgrowth, indicating the existence of a GEF activity-independent role of Rabin8. The Arf6/Rab8-positive recycling endosomes (Arf6/Rab8-REs) and Rab10/Rab11-positive REs (Rab10/Rab11-REs) in NGF-stimulated PC12 cells are differently distributed. Rabin8 localizes on both RE populations and appears to activate Rab8 and Rab10 there. These localizations and functions of Rabin8 are Rab11 dependent. Thus Rabin8 regulates neurite outgrowth both by coordinating with Rab8, Rab10, and Rab11 and by a GEF activity-independent mechanism.
机译:膜贩运事件的许多方面是由Rab家族的小GTP酶调节的。神经突的生长需要通过膜运输将大量的蛋白质和脂质添加到生长的神经突的尖端,尽管在此过程中涉及了多个Rab,包括Rab8,Rab10和Rab11,但对神经突生长期间其调控机制的了解却很少。在这里,我们显示Rabin8,Rab8-鸟嘌呤核苷酸交换因子(GEF),调节神经生长因子(NGF)诱导的PC12细胞神经突生长。击倒Rabin8会抑制神经突增生,而过表达会促进神经突增生。我们还发现Rab10是Rabin8的新型底物,并且Rab8和Rab10都在Rabin8下游的神经突向外生长期间起作用。然而,令人惊讶的是,Rabin8的GEF活性不足同工型也促进神经突向外生长,表明Rabin8的GEF活性不依赖于角色。 NGF刺激的PC12细胞中Arf6 / Rab8阳性的再循环内体(Arf6 / Rab8-REs)和Rab10 / Rab11阳性的RE(Rab10 / Rab11-REs)分布不同。 Rabin8定位在两个RE种群上,并似乎在那里激活Rab8和Rab10。 Rabin8的这些定位和功能取决于Rab11。因此,Rabin8通过与Rab8,Rab10和Rab11协调以及与GEF活性无关的机制来调节神经突的生长。

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