Bischof G, Cosentini E, Hamilton G, Riegler M, Zacherl J, Teleky B, Feil W, Schiessel R, Machen T E, Wenzl E
University Clinic of Surgery, Vienna, Austria.
Biochim Biophys Acta. 1996 Jun 13;1282(1):131-9. doi: 10.1016/0005-2736(96)00050-8.
Mechanisms of intracellular pH (pHi) regulation seem to be involved in cellular growth and cell division. Little is known about how extracellular acidosis, known to occur in central regions of solid tumors, or alkaline conditions affect pHi regulation in colonic tumors. pHi changes in the colonic adenocarcinoma cell-line SW-620 were recorded by spectrofluorimetric monitoring of the pH-sensitive, fluorescent dye BCECF, and proliferative activity was assessed by [3H]thymidine uptake. Resting pHi in Hepes-buffered solution was 7.53 +/- 0.01 (n = 36). Both 1 mM amiloride and Na(+)-free solution inhibited pHi recovery from acidification and decreased pHi in resting cells. In HCO3-/CO2-buffered media resting pH1 was 7.42 +/- 0.01 (n = 36). Recovery from acidification was Na(+)-dependent, CI(-)-independent, and only partially blocked by 1 mM amiloride. In the presence of amiloride and 200 microM H2DIDS pHi recovery was completely inhibited. In Na(+)-free solution pHi decreased from 7.44 +/- 0.04 to 7.29 +/- 0.03 (n = 6) and no alkalinization was observed in CI(-)-free medium. Addition of 5 microM tributyltin bromide (an anion/OH-exchange ionophore) caused pHi to decrease from 7.43 +/- 0.05 to 7.17 +/- 0.08 (n = 5). The effects of pH0 on steady-state pHi, pHi recovery from acidification and proliferative activity after 48 h were investigated by changing buffer [CO2] and [HCO3-]. In general, increases in pH0 between 6.7 and 7.4 increased pHi recovery, steady-state pHi and growth rates. In summary, SW-620 cells have a resting pHi > 7.4 at 25 degrees C, which is higher than other intestinal cells. Acid extrusion in physiological bicarbonate media is accomplished by a pHi-sensitive Na+/H+ exchanger and a pHi-insensitive Na(+)-HCO3-cotransporter, both of which are operational in control cells at the resting pHi. No evidence for activity of a CI-/HCO3- exchanger was found in these cells, which could account for the high pHi observed and may explain why the cells continue to grow in acidic tumor environments.
细胞内pH值(pHi)调节机制似乎与细胞生长和细胞分裂有关。对于实体瘤中心区域出现的细胞外酸中毒或碱性条件如何影响结肠肿瘤中的pHi调节,人们了解甚少。通过对pH敏感的荧光染料BCECF进行荧光分光光度监测,记录结肠腺癌细胞系SW - 620中的pHi变化,并通过[³H]胸苷摄取评估增殖活性。在Hepes缓冲溶液中静息pHi为7.53±0.01(n = 36)。1 mM氨氯吡脒和无钠溶液均抑制pHi从酸化状态恢复,并降低静息细胞的pHi。在HCO₃⁻/CO₂缓冲介质中,静息pH1为7.42±0.01(n = 36)。从酸化状态恢复是钠依赖性的,氯非依赖性的,并且仅被1 mM氨氯吡脒部分阻断。在氨氯吡脒和200 μM H2DIDS存在下,pHi恢复被完全抑制。在无钠溶液中,pHi从7.44±0.04降至7.29±0.03(n = 6),并且在无氯介质中未观察到碱化现象。添加5 μM三丁基溴化锡(一种阴离子/OH交换离子载体)导致pHi从7.43±0.05降至7.17±0.08(n = 5)。通过改变缓冲液中的[CO₂]和[HCO₃⁻],研究了pH0对48小时后稳态pHi、pHi从酸化状态恢复以及增殖活性的影响。一般来说,pH0在6.7至7.4之间升高会增加pHi恢复、稳态pHi和生长速率。总之,SW - 620细胞在25℃时静息pHi>7.4,高于其他肠道细胞。在生理碳酸氢盐介质中酸排出是通过一个对pHi敏感的Na⁺/H⁺交换体和一个对pHi不敏感的Na⁺-HCO₃协同转运体完成的,这两者在静息pHi时在对照细胞中都起作用。在这些细胞中未发现CI⁻/HCO₃⁻交换体活性的证据,这可以解释所观察到的高pHi,并可能解释为什么细胞在酸性肿瘤环境中继续生长。