Morris C E, Homann U
Department of Medicine, University of Ottawa, Neuroscience, Loeb Health Research Institute, Ottawa Hospital, Ontario, Canada.
J Membr Biol. 2001 Jan 15;179(2):79-102. doi: 10.1007/s002320010040.
The beautifully orchestrated regulation of cell shape and volume are central themes in cell biology and physiology. Though it is less well recognized, cell surface area regulation also constitutes a distinct task for cells. Maintaining an appropriate surface area is no automatic side effect of volume regulation or shape change. The issue of surface area regulation (SAR) would be moot if all cells resembled mammalian erythrocytes in being constrained to change shape and volume using existing surface membrane. But these enucleate cells are anomalies, possessing no endomembrane. Most cells use endomembrane to continually rework their plasma membrane, even while maintaining a given size or shape. This membrane traffic is intensively studied, generally with the emphasis on targeting and turnover of proteins and delivery of vesicle contents. But surface area (SA) homeostasis, including the controlled increase or decrease of SA, is another of the outcomes of trafficking. Our principal aims, then, are to highlight SAR as a discrete cellular task and to survey evidence for the idea that membrane tension is central to the task. Cells cannot directly "measure" their volume or SA, yet must regulate both. We posit that a homeostatic relationship exists between plasma membrane tension and plasma membrane area, which implies that cells detect and respond to deviations around a membrane tension set point. Maintenance of membrane strength during membrane turnover, a seldom-addressed aspect of SA dynamics, we examine in the context of SAR. SAR occurs in both animal and plant cells. The review shows the latter to be a continuing source of groundbreaking work on tension-sensitive SAR, but is principally slanted to animal cells.
细胞形状和体积的精确调控是细胞生物学和生理学的核心主题。尽管细胞表面积调控这一概念尚未得到广泛认可,但它同样是细胞面临的一项独特任务。维持适当的表面积并非体积调控或形状改变的必然附带结果。如果所有细胞都像哺乳动物红细胞那样,只能利用现有的细胞膜来改变形状和体积,那么表面积调控(SAR)的问题就没有讨论的必要了。但这些无核细胞是特例,它们没有内膜系统。大多数细胞即使在保持特定大小或形状时,也会利用内膜系统不断重塑其质膜。人们对这种膜运输进行了深入研究,通常重点关注蛋白质的靶向定位、周转以及囊泡内容物的递送。然而,包括表面积的可控增减在内的表面积(SA)稳态是膜运输的另一个结果。因此,我们的主要目的是强调表面积调控是一项独立的细胞任务,并梳理支持膜张力是这一任务核心的相关证据。细胞无法直接“测量”其体积或表面积,但必须对两者进行调控。我们假定质膜张力和质膜面积之间存在一种稳态关系,这意味着细胞能够检测并响应膜张力设定点附近的偏差。我们将在表面积调控的背景下,探讨膜周转过程中膜强度的维持,这是表面积动态变化中一个很少被提及的方面。表面积调控在动物和植物细胞中均会发生。这篇综述表明植物细胞在对张力敏感的表面积调控方面一直是开创性研究的持续来源,但主要还是侧重于动物细胞。