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2
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Effects of dynein on microtubule mechanics and centrosome positioning.动力蛋白对微管力学和中心体定位的影响。
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本文引用的文献

1
Analysis of the Role of Astral Rays in Pronuclear Migration in Sand Dollar Eggs by the Colcemid-UV Method: (sperm aster/pronuclear migration/sand dollar/colcemid-UV method).用秋水仙酰胺-紫外线法分析海胆卵中星体射线在原核迁移中的作用:(精子星体/原核迁移/海胆/秋水仙酰胺-紫外线法)
Dev Growth Differ. 1986 Apr;28(2):143-156. doi: 10.1111/j.1440-169X.1986.00143.x.
2
Cell cycle-regulated cortical dynein/dynactin promotes symmetric cell division by differential pole motion in anaphase.细胞周期调控的皮层动力蛋白/动力蛋白激活因子通过在后期的两极运动的差异促进对称细胞分裂。
Mol Biol Cell. 2012 Sep;23(17):3380-90. doi: 10.1091/mbc.E12-02-0109. Epub 2012 Jul 18.
3
Nuclear positioning: dynein needed for microtubule shrinkage-coupled movement.核定位:微管收缩耦联运动需要动力蛋白。
Curr Biol. 2012 Jun 19;22(12):R496-9. doi: 10.1016/j.cub.2012.04.044.
4
Mechanism for astral microtubule capture by cortical Bud6p priming spindle polarity in S. cerevisiae.星状微管通过 Bud6p 对皮层的预定位捕获机制来决定酵母的纺锤体极性。
Curr Biol. 2012 Jun 19;22(12):1075-83. doi: 10.1016/j.cub.2012.04.059. Epub 2012 May 17.
5
Dynein tethers and stabilizes dynamic microtubule plus ends.动力蛋白将和稳定动态微管的正端。
Curr Biol. 2012 Apr 10;22(7):632-7. doi: 10.1016/j.cub.2012.02.023. Epub 2012 Mar 22.
6
Cortical dynein controls microtubule dynamics to generate pulling forces that position microtubule asters.皮质动力蛋白控制微管动力学,产生牵拉微管星体的力。
Cell. 2012 Feb 3;148(3):502-14. doi: 10.1016/j.cell.2012.01.007.
7
Effects of dynein on microtubule mechanics and centrosome positioning.动力蛋白对微管力学和中心体定位的影响。
Mol Biol Cell. 2011 Dec;22(24):4834-41. doi: 10.1091/mbc.E11-07-0611. Epub 2011 Oct 19.
8
Encapsulation of active cytoskeletal protein networks in cell-sized liposomes.细胞大小脂质体中活性细胞骨架蛋白网络的包封。
Langmuir. 2011 Aug 16;27(16):10061-71. doi: 10.1021/la201604z. Epub 2011 Jul 12.
9
A polarised population of dynamic microtubules mediates homeostatic length control in animal cells.动态微管的极化群体介导动物细胞的自主长度控制。
PLoS Biol. 2010 Nov 16;8(11):e1000542. doi: 10.1371/journal.pbio.1000542.
10
Caenorhabditis elegans EFA-6 limits microtubule growth at the cell cortex.秀丽隐杆线虫 EFA-6 限制细胞皮层处的微管生长。
Nat Cell Biol. 2010 Dec;12(12):1235-41. doi: 10.1038/ncb2128. Epub 2010 Nov 14.

纵向微管-动力蛋白相互作用和基于牵拉的微管组织中心定位。

End-on microtubule-dynein interactions and pulling-based positioning of microtubule organizing centers.

机构信息

Faculty of Arts and Sciences, Center for Systems Biology, Harvard University, Cambridge, MA, USA.

出版信息

Cell Cycle. 2012 Oct 15;11(20):3750-7. doi: 10.4161/cc.21753. Epub 2012 Aug 16.

DOI:10.4161/cc.21753
PMID:22895049
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3495818/
Abstract

During important cellular processes such as centrosome and spindle positioning, dynein at the cortex interacts with dynamic microtubules in an apparent "end-on" fashion. It is well-established that dynein can generate forces by moving laterally along the microtubule lattice, but much less is known about dynein's interaction with dynamic microtubule ends. In this paper, we review recent in vitro experiments that show that dynein, attached to an artificial cortex, is able to capture microtubule ends, regulate microtubule dynamics and mediate the generation of pulling forces on shrinking microtubules. We further review existing ideas on the involvement of dynein-mediated cortical pulling forces in the positioning of microtubule organizing centers such as centrosomes. Recent in vitro experiments have demonstrated that cortical pulling forces in combination with pushing forces can lead to reliable centering of microtubule asters in quasi two-dimensional microfabricated chambers. In these experiments, pushing leads to slipping of microtubule ends along the chamber boundaries, resulting in an anisotropic distribution of cortical microtubule contacts that favors centering, once pulling force generators become engaged. This effect is predicted to be strongly geometry-dependent, and we therefore finally discuss ongoing efforts to repeat these experiments in three-dimensional, spherical and deformable geometries.

摘要

在中心体和纺锤体定位等重要细胞过程中,皮层中的动力蛋白以明显的“端到端”方式与动态微管相互作用。动力蛋白可以通过沿微管晶格侧向移动来产生力,这一点已经得到充分证实,但关于动力蛋白与动态微管末端的相互作用知之甚少。在本文中,我们回顾了最近的体外实验,这些实验表明,附着在人工皮层上的动力蛋白能够捕获微管末端,调节微管动力学,并介导对收缩微管的拉力的产生。我们进一步回顾了关于动力蛋白介导的皮层拉力在微管组织中心(如中心体)定位中的作用的现有观点。最近的体外实验表明,皮层拉力与推力相结合可以导致微管星状体在准二维微加工腔室内可靠地居中。在这些实验中,推动导致微管末端沿着腔室边界滑动,从而导致皮层微管接触的各向异性分布,有利于居中,一旦拉力发生器开始工作。这种效应预计强烈依赖于几何形状,因此我们最后讨论了在三维、球形和可变形几何形状中重复这些实验的进展。