Cosson P, de Curtis I, Pouysségur J, Griffiths G, Davoust J
European Molecular Biology Laboratory, Heidelberg, Federal Republic of Germany.
J Cell Biol. 1989 Feb;108(2):377-87. doi: 10.1083/jcb.108.2.377.
A fibroblast mutant cell line lacking the Na+/H+ antiporter was used to study the influence of low cytoplasmic pH on membrane transport in the endocytic and exocytic pathways. After being loaded with protons, the mutant cells were acidified at pH 6.2 to 6.8 for 20 min while the parent cells regulated their pH within 1 min. Cytoplasmic acidification did not affect the level of intracellular ATP or the number of clathrin-coated pits at the cell surface. However, cytosolic acidification below pH 6.8 blocked the uptake of two fluid phase markers, Lucifer Yellow and horseradish peroxidase, as well as the internalization and the recycling of transferrin. When the cytoplasmic pH was reversed to physiological values, both fluid phase endocytosis and receptor-mediated endocytosis resumed with identical kinetics. Low cytoplasmic pH also inhibited the rate of intracellular transport from the Golgi complex to the plasma membrane. This was shown in cells infected by the temperature-sensitive mutant ts 045 of the vesicular stomatitis virus (VSV) using as a marker of transport the mutated viral membrane glycoprotein (VSV-G protein). The VSV-G protein was accumulated in the trans-Golgi network (TGN) by an incubation at 19.5 degrees C and was transported to the cell surface upon shifting the temperature to 31 degrees C. This transport was arrested in acidified cells maintained at low cytosolic pH and resumed during the recovery phase of the cytosolic pH. Electron microscopy performed on epon and cryo-sections of mutant cells acidified below pH 6.8 showed that the VSV-G protein was present in the TGN. These results indicate that acidification of the cytosol to a pH less than 6.8 inhibits reversibly membrane transport in both endocytic and exocytic pathways. In all likelihood, the clathrin and nonclathrin coated vesicles that are involved in endo- and exocytosis cannot pinch off from the cell surface or from the TGN below this critical value of internal pH.
利用一种缺乏Na⁺/H⁺逆向转运蛋白的成纤维细胞突变细胞系,研究低细胞质pH对胞吞和胞吐途径中膜转运的影响。在用质子加载后,突变细胞在pH 6.2至6.8下酸化20分钟,而亲代细胞在1分钟内调节其pH。细胞质酸化不影响细胞内ATP水平或细胞表面网格蛋白包被小窝的数量。然而,细胞质酸化至pH 6.8以下会阻断两种液相标记物(路西法黄和辣根过氧化物酶)的摄取,以及转铁蛋白的内化和循环利用。当细胞质pH恢复到生理值时,液相内吞作用和受体介导的内吞作用均以相同的动力学恢复。低细胞质pH也抑制了从高尔基体复合体到质膜的细胞内转运速率。这在感染水泡性口炎病毒(VSV)温度敏感突变体ts 045的细胞中得到证实,使用突变的病毒膜糖蛋白(VSV-G蛋白)作为转运标记物。VSV-G蛋白在19.5℃孵育时积聚在反式高尔基体网络(TGN)中,并在温度升至31℃时转运至细胞表面。这种转运在维持低细胞质pH的酸化细胞中被阻断,并在细胞质pH的恢复阶段恢复。对酸化至pH 6.8以下的突变细胞的环氧树脂包埋和冷冻切片进行电子显微镜检查显示,VSV-G蛋白存在于TGN中。这些结果表明,细胞质酸化至pH小于6.8会可逆地抑制胞吞和胞吐途径中的膜转运。极有可能的是,参与内吞和外排作用的网格蛋白包被囊泡和非网格蛋白包被囊泡在内部pH低于这个临界值时无法从细胞表面或TGN脱离。