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利用基于钙黏蛋白黏附的数学模型来理解肌动蛋白细胞骨架的功能。

Using a mathematical model of cadherin-based adhesion to understand the function of the actin cytoskeleton.

作者信息

Dallon J C, Newren Elijah, Hansen Marc D H

机构信息

Department of Mathematics, Brigham Young University, TMCB 312, Provo, Utah 84602-6539, USA.

出版信息

Phys Rev E Stat Nonlin Soft Matter Phys. 2009 Mar;79(3 Pt 1):031918. doi: 10.1103/PhysRevE.79.031918. Epub 2009 Mar 27.

Abstract

The actin cytoskeleton plays a role in cell-cell adhesion but its specific function is not clear. Actin might anchor cadherins or drive membrane protrusions in order to facilitate cell-cell adhesion. Using a mathematical model of the forces involved in cadherin-based adhesion, we investigate its possible functions. The immersed boundary method is used to model the cell membrane and cortex with cadherin binding forces added as linear springs. The simulations indicate that cells in suspension can develop normal cell-cell contacts without actin-based cadherin anchoring or membrane protrusions. The cadherins can be fixed in the membrane or free to move, and the end results are similar. For adherent cells, simulations suggest that the actin cytoskeleton must play an active role for the cells to establish cell-cell contact regions similar to those observed in vitro.

摘要

肌动蛋白细胞骨架在细胞间黏附中发挥作用,但其具体功能尚不清楚。肌动蛋白可能锚定钙黏蛋白或驱动膜突起,以促进细胞间黏附。我们使用基于钙黏蛋白黏附所涉及力的数学模型来研究其可能的功能。采用浸入边界方法对细胞膜和皮质进行建模,并将钙黏蛋白结合力作为线性弹簧添加进去。模拟结果表明,悬浮细胞无需基于肌动蛋白的钙黏蛋白锚定或膜突起就能形成正常的细胞间接触。钙黏蛋白可以固定在膜中或自由移动,最终结果相似。对于贴壁细胞,模拟表明肌动蛋白细胞骨架必须发挥积极作用,细胞才能建立类似于体外观察到的细胞间接触区域。

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