Jamieson G A, Frazier W A, Schlesinger P H
J Cell Biol. 1984 Nov;99(5):1883-7. doi: 10.1083/jcb.99.5.1883.
The intracellular pH (pHi) of Dictyostelium discoideum amebae has been determined using the pH-dependent fluorescence of intracellularly trapped fluorescein (Thomas, J. A., R. N. Buschbaum, A. Zimiak, and E. Racker, Biochemistry, 18:2210-2218). The pHi of cells measured 45-60 min after initiation of differentiation was between 6.2 and 6.3. At approximately 2 h into differentiation cells underwent a transient intracellular alkalinization during which the pHi rose to 7.13 (+/- 0.3, n = 4), after which the pHi returned to approximately the original value (6.2-6.4). Cells that were removed from growth medium but were incubated in differentiation medium containing 3% dextrose did not exhibit this transient increase in pHi. The alkalinization event can also be prevented from occurring by differentiation in Na+-free solutions or by the addition of amiloride to sodium-containing buffer solutions, suggesting that the alkalinization is sodium dependent. When the alkalinization was prevented by amiloride treatment, cells did not progress normally into differentiation. This increase in pHi was initiated by the cells 2 h after removal from nutrient medium and it could be inhibited by several treatments that had been observed to delay the differentiation program, suggesting that it plays a major role in the initiation of the developmental program of this organism.
利用细胞内捕获的荧光素的pH依赖性荧光,测定了盘基网柄菌变形虫的细胞内pH值(pHi)(Thomas,J. A.,R. N. Buschbaum,A. Zimiak和E. Racker,《生物化学》,18:2210 - 2218)。分化开始后45 - 60分钟测量的细胞pHi在6.2至6.3之间。在分化约2小时时,细胞经历了短暂的细胞内碱化,在此期间pHi升至7.13(±0.3,n = 4),之后pHi恢复到大致原始值(6.2 - 6.4)。从生长培养基中取出但在含有3%葡萄糖的分化培养基中孵育的细胞未表现出这种pHi的短暂升高。在无钠溶液中分化或向含钠缓冲溶液中添加氨氯吡咪也可防止碱化事件发生,这表明碱化依赖于钠。当通过氨氯吡咪处理防止碱化时,细胞不能正常进入分化阶段。从营养培养基中取出2小时后,细胞开始出现这种pHi升高,并且它可被几种已观察到会延迟分化程序的处理所抑制,这表明它在该生物体发育程序的启动中起主要作用。