Hobdy-Henderson Karen C, Hales Chadwick M, Lapierre Lynne A, Cheney Richard E, Goldenring James R
Department of Surgery, Vanderbilt University School of Medicine, Nashville, TN 37232, USA.
Traffic. 2003 Oct;4(10):681-93. doi: 10.1034/j.1600-0854.2003.00124.x.
The members of the family of Rab11 small GTPases are critical regulators of the plasma membrane vesicle recycling system. While previous studies have determined that the Golgi apparatus disperses during mitosis and reorganizes after cytokinesis, the fate of the recycling system during the cell cycle is more obscure. We have now studied in MDCK cells the fate during mitosis of an apical recycling system cargo, the polymeric IgA receptor (pIgAR), and regulators of the recycling system, Rab11a and its interacting proteins myosin Vb, Rab11-FIP1, Rab11-FIP2 and pp75/Rip11. Rab11a, pIgAR and myosin Vb containing vesicles dispersed into diffuse puncta in the cytosol during prophase and then became clustered near the spindle poles after metaphase, increasing in intensity throughout telophase. A similar pattern was observed for Rab11-FIP1 and Rab11-FIP2. However, Rab11-FIP1 lost colocalization with other recycling system markers during late prophase, relocating to the pericentriolar material. During telophase, Rab11-FIP1 returned to recycling system vesicles. Western blot analysis indicated that both Rab11a and pIgAR remained associated with membrane vesicles throughout the cell cycle. This behavior of the Rab11a-containing apical recycling endosome system during division was distinct from that of the Golgi apparatus. These results indicate that critical components of the apical recycling system remain associated on vesicles throughout the cell cycle and may provide a means for rapid re-establishment of plasma membrane components after mitosis.
Rab11小GTP酶家族成员是质膜囊泡循环系统的关键调节因子。虽然先前的研究已经确定高尔基体在有丝分裂期间分散,并在胞质分裂后重新组织,但循环系统在细胞周期中的命运仍较为模糊。我们现在在MDCK细胞中研究了顶端循环系统货物——聚合免疫球蛋白A受体(pIgAR),以及循环系统调节因子Rab11a及其相互作用蛋白肌球蛋白Vb、Rab11-FIP1、Rab11-FIP2和pp75/Rip11在有丝分裂期间的命运。含有Rab11a、pIgAR和肌球蛋白Vb的囊泡在前期分散到胞质溶胶中的弥散斑点中,然后在中期后聚集在纺锤体极附近,在末期强度增加。Rab11-FIP1和Rab11-FIP2也观察到类似模式。然而,Rab11-FIP1在前期后期与其他循环系统标记物失去共定位,重新定位到中心粒周围物质。在末期,Rab11-FIP1回到循环系统囊泡。蛋白质印迹分析表明,Rab11a和pIgAR在整个细胞周期中都与膜囊泡相关。在分裂过程中,含Rab11a的顶端循环内体系统的这种行为与高尔基体不同。这些结果表明,顶端循环系统的关键成分在整个细胞周期中都与囊泡相关,并可能为有丝分裂后质膜成分的快速重建提供一种方式。