Strickland L I, Wen Y, Gundersen G G, Burgess D R
Department of Biology, Boston College, Chestnut Hill, Massachusetts 02467, USA.
Curr Biol. 2005 Dec 20;15(24):2249-55. doi: 10.1016/j.cub.2005.10.073.
In animal cells, microtubules (MTs) of the mitotic apparatus (MA) communicate with the cell cortex to stimulate cytokinesis; however, the molecular nature of this stimulus remains elusive . A signal for cytokinesis likely involves the MT plus end binding family of proteins, which includes EB1, p150glued, APC, LIS1, and CLIP-170. These proteins modulate MT dynamics and facilitate interactions between growing MTs and their intracellular targets, including kinetochores, organelles, and the cell cortex . The dynein-dynactin complex mediates many of these microtubule capture events . We report that EB1 and p150glued interactions are required for stimulation of cytokinesis in dividing sea urchin eggs. Injected antibodies against EB1 or p150glued suppressed furrow ingression but did not prevent elongation of anaphase astral MTs toward the cortex, suggesting that EB1 and dynactin are both required for communication between the MA and the cortex. Targeted disruption of the interaction between EB1 and p150glued suppressed anaphase astral MT elongation and resulted in a delay of cytokinesis that could not be overcome by manipulation of the asters toward the cortex. We conclude that EB1 and dynactin participate in stimulation of the cleavage furrow, and their interaction promotes elongation of astral MTs at anaphase onset.
在动物细胞中,有丝分裂器(MA)的微管(MTs)与细胞皮层相互作用以刺激胞质分裂;然而,这种刺激的分子本质仍然难以捉摸。胞质分裂信号可能涉及微管正端结合蛋白家族,其中包括EB1、p150glued、APC、LIS1和CLIP-170。这些蛋白调节微管动力学,并促进生长中的微管与其细胞内靶点之间的相互作用,这些靶点包括动粒、细胞器和细胞皮层。动力蛋白-动力蛋白激活蛋白复合体介导了许多此类微管捕获事件。我们报告称,EB1与p150glued的相互作用是海胆卵分裂过程中刺激胞质分裂所必需的。注射针对EB1或p150glued的抗体可抑制沟陷,但不会阻止后期星体微管向皮层延伸,这表明EB1和动力蛋白激活蛋白对于有丝分裂器与皮层之间的通讯都是必需的。靶向破坏EB1与p150glued之间的相互作用会抑制后期星体微管的延伸,并导致胞质分裂延迟,而通过将星体向皮层方向操作无法克服这种延迟。我们得出结论,EB1和动力蛋白激活蛋白参与了对分裂沟的刺激,并且它们之间的相互作用促进了后期开始时星体微管的延伸。