Pintsch T, Satre M, Klein G, Martin J B, Schuster S C
Max-Planck-Institute for Biochemistry, D-82152 Martinsried, Germany.
BMC Cell Biol. 2001;2:9. doi: 10.1186/1471-2121-2-9. Epub 2001 Jun 8.
Dictyostelium cells exhibit an unusual response to hyperosmolarity that is distinct from the response in other organisms investigated: instead of accumulating compatible osmolytes as it has been described for a wide range of organisms, Dictyostelium cells rearrange their cytoskeleton and thereby build up a rigid network which is believed to constitute the major osmoprotective mechanism in this organism. To gain more insight into the osmoregulation of this amoeba, we investigated physiological processes affected under hyperosmotic conditions in Dictyostelium.
We determined pH changes in response to hyperosmotic stress using FACS or 31P-NMR. Hyperosmolarity was found to acidify the cytosol from pH 7.5 to 6.8 within 5 minutes, whereas the pH of the endo-lysosomal compartment remained constant. Fluid-phase endocytosis was identified as a possible target of cytosolic acidification, as the inhibition of endocytosis observed under hypertonic conditions can be fully attributed to cytosolic acidification. In addition, a deceleration of vesicle mobility and a decrease in the NTP pool was observed.
Together, these results indicate that hyperosmotic stress triggers pleiotropic effects, which are partially mediated by a pH signal and which all contribute to the downregulation of cellular activity. The comparison of our results with the effect of hyperosmolarity and intracellular acidification on receptor-mediated endocytosis in mammalian cells reveals striking similarities, suggesting the hypothesis of the same mechanism of inhibition by low internal pH.
盘基网柄菌细胞对高渗胁迫表现出一种不同寻常的反应,这种反应与其他已研究的生物体的反应不同:与许多生物体中所描述的积累相容性溶质不同,盘基网柄菌细胞会重新排列其细胞骨架,从而形成一个刚性网络,据信这构成了该生物体主要的渗透保护机制。为了更深入了解这种变形虫的渗透调节,我们研究了盘基网柄菌在高渗条件下受影响的生理过程。
我们使用流式细胞仪或31P - NMR测定了对高渗胁迫的pH变化。发现高渗在5分钟内将细胞质溶胶的pH从7.5酸化至6.8,而内溶酶体区室的pH保持恒定。液相内吞作用被确定为细胞质酸化的一个可能靶点,因为在高渗条件下观察到的内吞作用抑制可完全归因于细胞质酸化。此外,还观察到囊泡移动性减慢和NTP池减少。
总之,这些结果表明高渗胁迫触发了多效性效应,这些效应部分由pH信号介导,并且都有助于细胞活性的下调。将我们的结果与高渗和细胞内酸化对哺乳动物细胞中受体介导的内吞作用的影响进行比较,发现了惊人的相似之处,这表明存在低细胞内pH抑制机制相同的假说。