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Phosphoinositides in the regulation of actin cortex and cell migration

机译:磷酸肌醇调节肌动蛋白皮层和细胞迁移

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In order for the cell to function well within a multicellular system, the mechanical properties of the plasma membrane need to meet two different requirements: cell shape maintenance and rearrangement. To achieve these goals, phosphoinositides play key roles in the regulation of the cortical actin cytoskeleton. PI(4,5)P-2 is the most abundant phosphoinositide species in the plasma membrane. It maintains cell shape by linking the actin cortex to the membrane via interactions with Ezrin/Radixin/Moesin (ERM) proteins and class I myosins. Although the role of D3-phosphoinositides, such as PI(3,4,5)P-3, in actin-driven cell migration has been a subject of controversy, it becomes evident that the dynamic turnover of the phosphoinositide by the action of metabolizing enzymes, such as 5-phosphatases, is necessary. Recent studies have revealed an important role of PI(3,4)P-2 in podosome/invadopodia formation, shedding new light on the actin-based organization of membrane structures regulated by phosphoinositide signaling. This article is part of a Special Issue entitled Phosphoinositides. (C) 2014 Elsevier B.V. All rights reserved.
机译:为了使细胞在多细胞系统中正常运行,质膜的机械性能需要满足两个不同的要求:细胞形状的维持和重排。为了实现这些目标,磷酸肌醇在调节皮质肌动蛋白细胞骨架中起关键作用。 PI(4,5)P-2是质膜中最丰富的磷酸肌醇物质。它通过与Ezrin / Radixin / Moesin(ERM)蛋白和I类肌球蛋白相互作用将肌动蛋白皮质连接到膜上,从而维持细胞形状。尽管D3-磷酸肌醇,如PI(3,4,5)P-3在肌动蛋白驱动的细胞迁移中的作用一直是一个有争议的话题,但很明显,磷酸肌醇通过代谢作用的动态更新必需的酶,例如5-磷酸酶。最近的研究已经揭示了PI(3,4)P-2在足小体/囊足形成中的重要作用,为磷酸肌醇信号传导调节的膜结构的基于肌动蛋白的组织结构提供了新的思路。本文是名为“磷酸肌醇”的特刊的一部分。 (C)2014 Elsevier B.V.保留所有权利。

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