Department of Cell and Developmental Biology, School of Medicine, Anschutz Medical Campus, University of Colorado Denver, Aurora, Colorado 80045, USA.
Nat Cell Biol. 2012 Oct;14(10):1068-78. doi: 10.1038/ncb2577. Epub 2012 Sep 23.
The final cytokinesis event involves severing of the connecting intercellular bridge (ICB) between daughter cells. FIP3-positive recycling endosomes (FIP3 endosomes) and ESCRT complexes have been implicated in mediating the final stages of cytokinesis. Here we analyse the spatiotemporal dynamics of the actin cytoskeleton, FIP3-endosome fusion and ESCRT-III localization during cytokinesis to show that the ICB narrows by a FIP3-endosome-mediated secondary ingression, whereas the ESCRT-III complex is needed only for the last scission step of cytokinesis. We characterize the role of FIP3 endosomes during cytokinesis to demonstrate that FIP3 endosomes deliver SCAMP2/3 and p50RhoGAP to the ICB during late telophase, proteins required for the formation of the secondary ingression. We also show that the FIP3-endosome-induced secondary ingression is required for the recruitment of the ESCRT-III complex to the abscission site. Finally, we characterize a FIP3-endosome-dependent regulation of the ICB cortical actin network through the delivery of p50RhoGAP. These results provide a framework for the coordinated efforts of actin, FIP3 endosomes and the ESCRTs to regulate cytokinesis and abscission.
最后一个胞质分裂事件涉及到切断子细胞之间的连接细胞桥(ICB)。已经有研究表明,FIP3 阳性再循环内体(FIP3 内体)和 ESCRT 复合物在介导胞质分裂的最后阶段中起作用。在这里,我们分析了胞质分裂过程中肌动蛋白细胞骨架、FIP3-内体融合和 ESCRT-III 定位的时空动态,结果表明 ICB 通过 FIP3-内体介导的二次内陷变窄,而 ESCRT-III 复合物仅在胞质分裂的最后一个断裂步骤中是必需的。我们研究了 FIP3 内体在胞质分裂中的作用,结果表明 FIP3 内体在晚期末期将 SCAMP2/3 和 p50RhoGAP 递送到 ICB,这两种蛋白是形成二次内陷所必需的。我们还表明,FIP3-内体诱导的二次内陷对于 ESCRT-III 复合物向分裂位点的招募是必需的。最后,我们通过 p50RhoGAP 的递送,描述了 FIP3 内体依赖性的 ICB 皮质肌动蛋白网络的调节。这些结果为肌动蛋白、FIP3 内体和 ESCRTs 协调努力调节胞质分裂和分裂提供了一个框架。