Department of Biological Sciences, Kent State University, Kent, OH, USA,
Department of Biological Sciences, Kent State University, Kent, OH, USA.
Cell Physiol Biochem. 2021 Jan 2;55(S1):25-40. doi: 10.33594/000000319.
High density of intracellular macromolecules creates a special condition known as macromolecular crowding (MC). One well-established consequence of MC is that only a slight change in the concentration of macromolecules (e.g., proteins) results in a shift of chemical equilibria towards the formation of macromolecular complexes and oligomers. This suggests a physiological mechanism of converting cell density changes into cellular responses. In this review, we start by providing a general overview of MC; then we examine the available experimental evidence that MC may act as a direct signaling factor in several types of cellular activities: mechano- and osmosensing, cell volume recovery in anisosmotic solutions, and apoptotic shrinkage. The latter phenomenon is analyzed in particular detail, as persistent shrinkage is known both to cause apoptosis and to occur during apoptosis resulting from other stimuli. We point to specific apoptotic reactions that involve formation of macromolecular complexes and, therefore, may provide a link between shrinkage and downstream responses.
细胞内大分子的高密度会产生一种特殊的状态,称为大分子拥挤(MC)。MC 的一个既定后果是,仅大分子(例如蛋白质)浓度的微小变化就会导致化学平衡向形成大分子复合物和低聚物的方向移动。这表明了一种将细胞密度变化转化为细胞反应的生理机制。在这篇综述中,我们首先提供了 MC 的概述;然后我们检查了现有的实验证据,表明 MC 可能作为几种类型的细胞活动的直接信号因子发挥作用:机械和渗透感应、非等渗溶液中的细胞体积恢复以及凋亡性收缩。特别详细地分析了后一种现象,因为已知持续收缩既会导致细胞凋亡,也会在其他刺激引起的细胞凋亡过程中发生。我们指出了涉及大分子复合物形成的特定凋亡反应,因此,可能在收缩和下游反应之间提供了联系。