Rink Jochen, Ghigo Eric, Kalaidzidis Yannis, Zerial Marino
Max Planck Institute of Molecular Cell Biology and Genetics, Pfotenhauerstrasse 108, 01307 Dresden, Germany.
Cell. 2005 Sep 9;122(5):735-49. doi: 10.1016/j.cell.2005.06.043.
The mechanisms of endosome biogenesis and maintenance are largely unknown. The small GTPases Rab 5 and Rab 7 are key determinants of early and late endosomes, organizing effector proteins into specific membrane subdomains. Whether such Rab machineries are indefinitely maintained on membranes or can disassemble in the course of cargo transport is an open question. Here, we combined novel image-analysis algorithms with fast live-cell imaging. We found that the level of Rab 5 dynamically fluctuates on individual early endosomes, linked by fusion and fission events into a network in time. Within it, degradative cargo concentrates in progressively fewer and larger endosomes that migrate from the cell periphery to the center where Rab 5 is rapidly replaced with Rab 7. The class C VPS/HOPS complex, an established GEF for Rab 7, interacts with Rab 5 and is required for Rab 5-to-Rab 7 conversion. Our results reveal unexpected dynamics of Rab domains and suggest Rab conversion as the mechanism of cargo progression between early and late endosomes.
内体生物发生和维持的机制在很大程度上尚不清楚。小GTP酶Rab 5和Rab 7是早期和晚期内体的关键决定因素,它们将效应蛋白组织到特定的膜亚结构域中。这种Rab机制是在膜上无限期维持,还是会在货物运输过程中解体,这是一个悬而未决的问题。在这里,我们将新颖的图像分析算法与快速活细胞成像相结合。我们发现,Rab 5的水平在单个早期内体上动态波动,通过融合和裂变事件及时连接成一个网络。在这个网络中,降解性货物集中在越来越少但越来越大的内体中,这些内体从细胞周边迁移到中心,在那里Rab 5迅速被Rab 7取代。C类VPS/HOPS复合物是一种既定的Rab 7鸟苷酸交换因子,它与Rab 5相互作用,是Rab 5向Rab 7转化所必需的。我们的结果揭示了Rab结构域出人意料的动态变化,并表明Rab转化是货物在早期和晚期内体之间进展的机制。