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由肌动蛋白聚合的弯曲激活物驱动的细胞膜波的传播。

Propagating cell-membrane waves driven by curved activators of actin polymerization.

机构信息

Department of Chemical Physics, the Weizmann Institute of Science, Rehovot, Israel.

出版信息

PLoS One. 2011 Apr 21;6(4):e18635. doi: 10.1371/journal.pone.0018635.

Abstract

Cells exhibit propagating membrane waves which involve the actin cytoskeleton. One type of such membranal waves are Circular Dorsal Ruffles (CDR) which are related to endocytosis and receptor internalization. Experimentally, CDRs have been associated with membrane bound activators of actin polymerization of concave shape. We present experimental evidence for the localization of convex membrane proteins in these structures, and their insensitivity to inhibition of myosin II contractility in immortalized mouse embryo fibroblasts cell cultures. These observations lead us to propose a theoretical model which explains the formation of these waves due to the interplay between complexes that contain activators of actin polymerization and membrane-bound curved proteins of both types of curvature (concave and convex). Our model predicts that the activity of both types of curved proteins is essential for sustaining propagating waves, which are abolished when one type of curved activator is removed. Within this model waves are initiated when the level of actin polymerization induced by the curved activators is higher than some threshold value, which allows the cell to control CDR formation. We demonstrate that the model can explain many features of CDRs, and give several testable predictions. This work demonstrates the importance of curved membrane proteins in organizing the actin cytoskeleton and cell shape.

摘要

细胞表现出涉及肌动蛋白细胞骨架的传播膜波。这种膜波的一种类型是环形背侧皱襞(CDR),与胞吞作用和受体内化有关。实验上,CDR 与膜结合的肌动蛋白聚合激活物的凹形有关。我们提出了实验证据,证明在这些结构中存在凸形膜蛋白的定位,以及它们对永生小鼠胚胎成纤维细胞培养物中肌球蛋白 II 收缩性抑制的不敏感性。这些观察结果使我们提出了一个理论模型,该模型解释了由于包含肌动蛋白聚合激活物和两种类型曲率(凹形和凸形)的膜结合弯曲蛋白的复合物之间的相互作用而形成这些波。我们的模型预测,两种类型的弯曲蛋白的活性对于维持传播波是必不可少的,当一种类型的弯曲激活物被去除时,传播波就会被取消。在这个模型中,当由弯曲激活物诱导的肌动蛋白聚合水平高于某个阈值时,波就会被引发,这允许细胞控制 CDR 的形成。我们证明该模型可以解释 CDR 的许多特征,并给出了几个可测试的预测。这项工作表明了弯曲膜蛋白在组织肌动蛋白细胞骨架和细胞形状方面的重要性。

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