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本文引用的文献

1
Dynamics and morphology of microvilli driven by actin polymerization.由肌动蛋白聚合驱动的微绒毛的动力学与形态学
Phys Rev Lett. 2006 Jul 7;97(1):018101. doi: 10.1103/PhysRevLett.97.018101. Epub 2006 Jul 5.
2
The sensory and motor roles of auditory hair cells.听觉毛细胞的感觉和运动作用。
Nat Rev Neurosci. 2006 Jan;7(1):19-29. doi: 10.1038/nrn1828.
3
Mechanics and dynamics of actin-driven thin membrane protrusions.肌动蛋白驱动的薄膜突起的力学与动力学
Biophys J. 2006 Jan 1;90(1):65-76. doi: 10.1529/biophysj.105.071480. Epub 2005 Oct 7.
4
Balanced levels of Espin are critical for stereociliary growth and length maintenance.埃斯平(Espin)水平的平衡对于静纤毛的生长和长度维持至关重要。
Cell Motil Cytoskeleton. 2005 Nov;62(3):157-65. doi: 10.1002/cm.20094.
5
When size matters: the dynamic regulation of stereocilia lengths.尺寸为何重要:静纤毛长度的动态调节
Curr Opin Cell Biol. 2005 Feb;17(1):55-61. doi: 10.1016/j.ceb.2004.12.005.
6
Myosin-XVa is required for tip localization of whirlin and differential elongation of hair-cell stereocilia.肌球蛋白-XVa是whirlin尖端定位和毛细胞静纤毛差异伸长所必需的。
Nat Cell Biol. 2005 Feb;7(2):148-56. doi: 10.1038/ncb1219. Epub 2005 Jan 16.
7
Processive capping by formin suggests a force-driven mechanism of actin polymerization.Formin介导的持续性加帽表明肌动蛋白聚合存在一种力驱动机制。
J Cell Biol. 2004 Dec 20;167(6):1011-7. doi: 10.1083/jcb.200410017. Epub 2004 Dec 13.
8
Formin is a processive motor that requires profilin to accelerate actin assembly and associated ATP hydrolysis.formin是一种持续性马达蛋白,它需要肌动蛋白单体结合蛋白来加速肌动蛋白组装以及相关的ATP水解。
Cell. 2004 Oct 29;119(3):419-29. doi: 10.1016/j.cell.2004.09.039.
9
Formins coming into focus.
Dev Cell. 2004 Mar;6(3):312-4. doi: 10.1016/s1534-5807(04)00073-5.
10
An actin molecular treadmill and myosins maintain stereocilia functional architecture and self-renewal.肌动蛋白分子踏车模型和肌球蛋白维持静纤毛的功能结构和自我更新。
J Cell Biol. 2004 Mar 15;164(6):887-97. doi: 10.1083/jcb.200310055.

静纤毛和微绒毛形状与大小的动态控制。

Dynamical control of the shape and size of stereocilia and microvilli.

作者信息

Prost Jacques, Barbetta Camilla, Joanny Jean-François

机构信息

Physico Chimie Curie, Institut Curie, Paris, France.

出版信息

Biophys J. 2007 Aug 15;93(4):1124-33. doi: 10.1529/biophysj.106.098038. Epub 2007 May 25.

DOI:10.1529/biophysj.106.098038
PMID:17526588
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1929046/
Abstract

We discuss theoretically the shape of actin-based protrusions such as stereocilia or microvilli that have important functions in many biological systems. These linear protrusions are dynamical structures continuously renewed by treadmilling: actin polymerizes at the tip of the cilium and depolymerizes in its bulk. They also often have a well-controlled length such as in the hair bundles of the inner ear cells where they appear in a graded staircase structure. Recent experimental results by another group of researchers show that the treadmilling velocity of the hair cell stereocilia is proportional to their length. We use generic arguments to describe the physics of stereocilia taking into account the effect of many individual proteins at a coarse-grained level by a few phenomenological parameters. At the tip of the cilium, we find that actin polymerization induces an effective pressure. Below the tip, the shape of the cilium is determined by depolymerization: Agreement with the observed shape requires that depolymerization occurs at least in two steps. Under these conditions, we calculate the cilium shape and provide physical grounds for the proportionality between treadmilling velocity and cilium length. We also calculate the penetration of the stereocilium in the actin cortical layer.

摘要

我们从理论上讨论了基于肌动蛋白的突起物的形状,比如静纤毛或微绒毛,它们在许多生物系统中都具有重要功能。这些线性突起物是通过肌动蛋白踏车运动不断更新的动态结构:肌动蛋白在纤毛尖端聚合,并在其主体部分解聚。它们通常还具有受到良好控制的长度,例如在内耳细胞的毛束中,它们呈现出分级阶梯结构。另一组研究人员最近的实验结果表明,毛细胞静纤毛的踏车运动速度与其长度成正比。我们运用一般论点来描述静纤毛的物理特性,通过一些唯象参数在粗粒化水平上考虑众多单个蛋白质的作用。在纤毛尖端,我们发现肌动蛋白聚合会产生有效压力。在尖端下方,纤毛的形状由解聚作用决定:要与观察到的形状相符,解聚至少需要分两步进行。在这些条件下,我们计算了纤毛的形状,并为踏车运动速度与纤毛长度之间的比例关系提供了物理依据。我们还计算了静纤毛在肌动蛋白皮质层中的穿透情况。