Piezo1, the new actor in cell volume regulation

A. Michelucci, L. Catacuzzeno
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Abstract

All animal cells control their volume through a complex set of mechanisms, both to counteract osmotic perturbations of the environment and to enable numerous vital biological processes, such as proliferation, apoptosis, and migration. The ability of cells to adjust their volume depends on the activity of ion channels and transporters which, by moving K+, Na+, and Cl ions across the plasma membrane, generate the osmotic gradient that drives water in and out of the cell. In 2010, Patapoutian’s group identified a small family of evolutionarily conserved, Ca2+-permeable mechanosensitive channels, Piezo1 and Piezo2, as essential components of the mechanically activated current that mediates mechanotransduction in vertebrates. Piezo1 is expressed in several tissues and its opening is promoted by a wide range of mechanical stimuli, including membrane stretch/deformation and osmotic stress. Piezo1-mediated Ca2+ influx is used by the cell to convert mechanical forces into cytosolic Ca2+ signals that control diverse cellular functions such as migration and cell death, both dependent on changes in cell volume and shape. The crucial role of Piezo1 in the regulation of cell volume was first demonstrated in erythrocytes, which need to reduce their volume to pass through narrow capillaries. In HEK293 cells, increased expression of Piezo1 was found to enhance the regulatory volume decrease (RVD), the process whereby the cell re-establishes its original volume after osmotic shock-induced swelling, and it does so through Ca2+-dependent modulation of the volume-regulated anion channels. More recently we reported that Piezo1 controls the RVD in glioblastoma cells via the modulation of Ca2+-activated K+ channels. To date, however, the mechanisms through which this mechanosensitive channel controls cell volume and maintains its homeostasis have been poorly investigated and are still far from being understood. The present review aims to provide a broad overview of the literature discussing the recent advances on this topic.

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Piezo1,细胞体积调节的新角色
所有动物细胞都通过一套复杂的机制来控制自身的体积,既能抵消环境中的渗透扰动,又能使增殖、凋亡和迁移等许多重要的生物过程得以进行。细胞调节自身体积的能力取决于离子通道和转运体的活性,它们通过在质膜上移动 K+、Na+ 和 Cl- 离子,产生渗透梯度,推动水分进出细胞。2010 年,Patapoutian 的研究小组发现了一小群进化保守的钙离子渗透性机械敏感通道--Piezo1 和 Piezo2,它们是介导脊椎动物机械传导的机械激活电流的重要组成部分。Piezo1 在多种组织中表达,它的开放受多种机械刺激的影响,包括膜的拉伸/变形和渗透压。细胞利用 Piezo1 介导的 Ca2+ 流入将机械力转化为细胞膜 Ca2+ 信号,从而控制迁移和细胞死亡等多种细胞功能,这两种功能都依赖于细胞体积和形状的变化。Piezo1 在细胞体积调节中的关键作用首先在红细胞中得到证实,红细胞需要缩小体积才能通过狭窄的毛细血管。在 HEK293 细胞中,我们发现增加 Piezo1 的表达能增强调节性体积缩小(RVD),这是细胞在渗透休克诱导的肿胀后重建其原始体积的过程,它是通过 Ca2+ 依赖性调节体积调节阴离子通道来实现的。最近,我们报道了 Piezo1 通过调节 Ca2+ 激活的 K+ 通道来控制胶质母细胞瘤细胞的 RVD。然而,迄今为止,人们对这种机械敏感通道控制细胞体积并维持其平衡的机制研究甚少,而且还远未搞清楚。本综述旨在对讨论该主题最新进展的文献进行概述。
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