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本文引用的文献

1
GMAP-210 recruits gamma-tubulin complexes to cis-Golgi membranes and is required for Golgi ribbon formation.GMAP-210将γ-微管蛋白复合体募集至顺式高尔基体膜,且是高尔基体带状结构形成所必需的。
Cell. 2004 Aug 6;118(3):323-35. doi: 10.1016/j.cell.2004.07.012.
2
Annexin 11 is required for midbody formation and completion of the terminal phase of cytokinesis.膜联蛋白11是中间体形成和胞质分裂末期完成所必需的。
J Cell Biol. 2004 Jun 21;165(6):813-22. doi: 10.1083/jcb.200311054. Epub 2004 Jun 14.
3
The RCP-Rab11 complex regulates endocytic protein sorting.RCP-Rab11复合体调节内吞蛋白分选。
Mol Biol Cell. 2004 Aug;15(8):3530-41. doi: 10.1091/mbc.e03-12-0918. Epub 2004 Jun 4.
4
Rab11-FIP3 localises to a Rab11-positive pericentrosomal compartment during interphase and to the cleavage furrow during cytokinesis.Rab11-FIP3在间期定位于Rab11阳性的中心体周围区室,在胞质分裂期间定位于分裂沟。
Biochem Biophys Res Commun. 2004 Jun 18;319(1):83-94. doi: 10.1016/j.bbrc.2004.04.157.
5
Pathways for membrane trafficking during cytokinesis.胞质分裂期间膜运输的途径。
Trends Cell Biol. 2004 Mar;14(3):115-8. doi: 10.1016/j.tcb.2004.01.006.
6
ARF6 controls post-endocytic recycling through its downstream exocyst complex effector.ARF6通过其下游的外泌体复合物效应器控制内吞后循环。
J Cell Biol. 2003 Dec 8;163(5):1111-21. doi: 10.1083/jcb.200305029.
7
Trafficking through Rab11 endosomes is required for cellularization during Drosophila embryogenesis.在果蝇胚胎发育过程中,通过Rab11内体的运输对于细胞化是必需的。
Curr Biol. 2003 Oct 28;13(21):1848-57. doi: 10.1016/j.cub.2003.10.023.
8
Rabs, Rips, FIPs, and endocytic membrane traffic.Rabs、Rips、FIPs与内吞膜运输
ScientificWorldJournal. 2003 Sep 15;3:870-80. doi: 10.1100/tsw.2003.69.
9
Actin cytoskeleton remodeling during early Drosophila furrow formation requires recycling endosomal components Nuclear-fallout and Rab11.果蝇早期沟形成过程中肌动蛋白细胞骨架重塑需要回收内体成分核沉降物和Rab11。
J Cell Biol. 2003 Oct 13;163(1):143-54. doi: 10.1083/jcb.200305115. Epub 2003 Oct 6.
10
Dynamics of the apical plasma membrane recycling system during cell division.细胞分裂过程中顶端质膜回收系统的动力学
Traffic. 2003 Oct;4(10):681-93. doi: 10.1034/j.1600-0854.2003.00124.x.

FIP3-Rab11蛋白复合物在胞质分裂后期调节回收型内体靶向至分裂沟。

The FIP3-Rab11 protein complex regulates recycling endosome targeting to the cleavage furrow during late cytokinesis.

作者信息

Wilson Gayle M, Fielding Andrew B, Simon Glenn C, Yu Xinzi, Andrews Paul D, Hames Rebecca S, Frey Andrew M, Peden Andrew A, Gould Gwyn W, Prekeris Rytis

机构信息

Department of Cellular and Developmental Biology, School of Medicine, University of Colorado Health Sciences Center, Denver, CO 80262, USA.

出版信息

Mol Biol Cell. 2005 Feb;16(2):849-60. doi: 10.1091/mbc.e04-10-0927. Epub 2004 Dec 15.

DOI:10.1091/mbc.e04-10-0927
PMID:15601896
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC545916/
Abstract

An integral part of cell division is the separation of daughter cells via cytokinesis. There is now good evidence that the completion of cytokinesis requires coordinated membrane trafficking to deliver new membrane to the tip of the furrow and to complete the abscission. Here we have examined membrane traffic in cytokinesis and describe several novel observations. First, we show that Rab11- and FIP3-containing recycling endosomes accumulate near the cleavage furrow and are required for successful completion of cytokinesis. Second, we demonstrate that the Rab11-FIP3 protein complex is intimately involved in the delivery of endosomes to the cleavage furrow. Significantly, although FIP3 recruitment to endosomes is Rab11 dependent, we find that the targeting of FIP3 to the midbody is independent of Rab11. Third, we show that the Rab11-FIP3 complex is required for a late stage of cytokinesis, possibly abscission. Finally, we demonstrate that localization of FIP3 is subject to substantial spatial and temporal regulation. These data provide the first detailed analysis of recycling endosomes in cell division and provide a new model for membrane traffic to the furrow. We propose that the dynamic Rab11-FIP3 interaction controls the delivery, targeting, and fusion of recycling endosomes with furrow during late cytokinesis and abscission.

摘要

细胞分裂的一个不可或缺的部分是通过胞质分裂来分离子细胞。现在有充分的证据表明,胞质分裂的完成需要协调的膜运输,以便将新的膜输送到沟的顶端并完成脱离。在这里,我们研究了胞质分裂中的膜运输,并描述了几个新的观察结果。首先,我们表明,含有Rab11和FIP3的回收型内体在分裂沟附近积累,并且是胞质分裂成功完成所必需的。其次,我们证明Rab11-FIP3蛋白复合物密切参与内体向分裂沟的运输。值得注意的是,虽然FIP3向内体的募集依赖于Rab11,但我们发现FIP3向中体的靶向独立于Rab11。第三,我们表明Rab11-FIP3复合物是胞质分裂后期(可能是脱离阶段)所必需的。最后,我们证明FIP3的定位受到大量的空间和时间调控。这些数据首次对细胞分裂中的回收型内体进行了详细分析,并为向沟的膜运输提供了一个新模型。我们提出,动态的Rab11-FIP3相互作用在胞质分裂后期和脱离过程中控制回收型内体向沟的运输、靶向和融合。