Boussouf A, Lambert R C, Gaillard S
Laboratoire de Neurobiologie Cellulaire, CNRS, Centre de Neurochimie, Strasbourg, France.
Glia. 1997 Jan;19(1):74-84. doi: 10.1002/(sici)1098-1136(199701)19:1<74::aid-glia8>3.0.co;2-a.
Intracellular pH (pHi) was measured at 37 degrees C in mature rat cerebellar oligodendrocytes dissociated in culture by using the pH-sensitive probe BCECF. Cells were identified by anti-galactocerebroside antibody. The mean steady-state pHi was 7.02 in the absence of CO2/bicarbonate (Hepes-buffered solution) at an external pH of 7.40 and 7.04 in 5% CO2/25 mM bicarbonate-buffered solution at the same external pH; this value was modified neither by the removal of external chloride nor by the addition of the chloride-coupled transport blocker DIDS. In both external solutions steady-state pHi values were strongly dependent on external pH. In Hepes-buffered solution pHi recovery following an acid load required external Na+ and was completely inhibited by amiloride, indicating the presence of a Na+/H+ exchanger. In CO2/bicarbonate-buffered solution amiloride partially reduced the pHi recovery rate, indicating the presence of a bicarbonate-dependent pHi regulating mechanism. Membrane depolarization induced by increasing external K+ concentration elicited an alkalinization only in the presence of external Na+ and bicarbonate. Analysis of the calculated HCO3- fluxes with respect to membrane potential indicated that these fluxes were mediated by a Na(+)-HCO3- cotransport with a stoichiometry of 1:3. These results demonstrate that a Na+/H+ exchanger and a Na(+)-HCO3- cotransporter are involved in pHi regulation of mature oligodendrocytes.
采用pH敏感探针BCECF,在37℃下对培养的成熟大鼠小脑少突胶质细胞的细胞内pH(pHi)进行了测量。通过抗半乳糖脑苷脂抗体对细胞进行鉴定。在外部pH值为7.40的无CO2/碳酸氢盐(Hepes缓冲溶液)条件下,平均稳态pHi为7.02;在相同外部pH值的5% CO2/25 mM碳酸氢盐缓冲溶液中,平均稳态pHi为7.04;该值不受外部氯离子去除或氯离子偶联转运阻滞剂DIDS添加的影响。在两种外部溶液中,稳态pHi值都强烈依赖于外部pH。在Hepes缓冲溶液中,酸负荷后pHi的恢复需要外部Na+,并被氨氯吡脒完全抑制,表明存在Na+/H+交换体。在CO2/碳酸氢盐缓冲溶液中,氨氯吡脒部分降低了pHi的恢复率,表明存在一种依赖碳酸氢盐的pHi调节机制。增加外部K+浓度引起的膜去极化仅在存在外部Na+和碳酸氢盐时引发碱化。关于膜电位对计算出的HCO3-通量的分析表明,这些通量是由化学计量比为1:3的Na(+)-HCO3-共转运介导的。这些结果表明,Na+/H+交换体和Na(+)-HCO3-共转运体参与了成熟少突胶质细胞的pHi调节。