Cantiello H F
Renal Unit, Massachusetts General Hospital East, Charlestown 02129, USA.
J Exp Zool. 1997 Dec 1;279(5):425-35. doi: 10.1002/(sici)1097-010x(19971201)279:5<425::aid-jez4>3.0.co;2-q.
The actin cytoskeleton is an intracellular structure, which is involved in the onset and control of cell shape and function. In order for this relevant network to control its own and thus cell volume, specific interactions between the actin cytoskeleton and ion channel regulation controlling intracellular salt and water homeostasis may be invoked. The hypotonic shock-induced, cell volume regulatory decrease (RVD) of most eukaryotic cells is a particularly useful example, as it is initiated and regulated by concerted processes involving both adaptive changes in actin filament organization and bulk fluid extrusion triggered by saline movement and the consequent decrease in cell water. The onset of RVD is linked to the selective activation of osmotically-sensitive ion channels and other relevant ion transport mechanisms involved in the net ionic movement from the cytosol. Such regulatory processes, entailing effector changes in actin filament organization which target the plasma membrane, are largely unknown. In this report, recent studies are summarized implicating dynamic changes in gel properties of the actin cytoskeleton as the effector mechanism in the regulation of ion channel activity, and thus cell volume, in human melanoma cells. Based on the characterization of the hypotonic cell volume regulatory response of human melanoma cells devoid of a functional actin-binding protein (ABP-280, a filamin homolog) and their genetically rescued counterpart transfected with a functional ABP, a hypothesis is raised which is consistent with a regulatory "sensory" mechanism based on the ability of actin networks to respond to changes in the intracellular water-salt homeostasis, which in turn effects signals controlling membrane function, including ion channel activity.
肌动蛋白细胞骨架是一种细胞内结构,参与细胞形状和功能的起始与控制。为了使这个相关网络控制自身进而控制细胞体积,可能需要肌动蛋白细胞骨架与控制细胞内盐和水平衡的离子通道调节之间的特定相互作用。大多数真核细胞的低渗休克诱导的细胞体积调节性减小(RVD)就是一个特别有用的例子,因为它是由协同过程启动和调节的,这些过程包括肌动蛋白丝组织的适应性变化以及由盐移动引发的大量液体挤出和随之而来的细胞内水分减少。RVD的起始与渗透敏感性离子通道的选择性激活以及参与从细胞质溶胶进行净离子移动的其他相关离子转运机制有关。这种涉及靶向质膜的肌动蛋白丝组织效应器变化的调节过程在很大程度上尚不清楚。在本报告中,总结了最近的研究,这些研究表明肌动蛋白细胞骨架凝胶特性的动态变化作为调节人黑色素瘤细胞中离子通道活性进而调节细胞体积的效应器机制。基于对缺乏功能性肌动蛋白结合蛋白(ABP - 280,一种细丝蛋白同源物)的人黑色素瘤细胞及其用功能性ABP转染的基因拯救对应物的低渗细胞体积调节反应的表征,提出了一个假设,该假设与基于肌动蛋白网络对细胞内水盐平衡变化做出反应的能力的调节“传感”机制一致,这反过来又影响控制膜功能(包括离子通道活性)的信号。