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培养的大鼠小脑浦肯野细胞内pH的离子调控

Ionic control of intracellular pH in rat cerebellar Purkinje cells maintained in culture.

作者信息

Gaillard S, Dupont J L

机构信息

Laboratoire d'Etude des Régulations Physiologiques, Université Louis Pasteur, Strasbourg, France.

出版信息

J Physiol. 1990 Jun;425:71-83. doi: 10.1113/jphysiol.1990.sp018093.

Abstract
  1. Intracellular pH (pHi) was measured in single rat cerebellar Purkinje cells maintained in primary culture using microspectrofluorescence analysis of the intracellularly trapped pH-sensitive dye 2',7'-bis-(2-carboxyethyl)-5 (and -6)-carboxyfluorescein (BCECF). 2. The ratio of the fluorescence signals measured at 530 nm in response to an alternating excitation at 450 and 490 nm was calibrated using the K(+)-H+ ionophore nigericin. This calibration gave a steady-state pHi of 7.06 +/- 0.02 (S.E.M., n = 17) when cells were perfused by a 5% CO2-25 mM-HCO3(-)-buffered solution at an external pH of 7.40 at 37 degrees C. 3. Replacement of external chloride with gluconate in the presence of bicarbonate induced a cytoplasmic alkalinization of about 0.3 pH unit. This alkalinization was independent of external sodium and was greatly reduced by 0.5 mM-DIDS, indicating the presence of a chloride-bicarbonate exchange. 4. In bicarbonate-free (HEPES-buffered) solution the steady-state pHi was 7.37 +/- 0.02 (n = 19), significantly higher than in bicarbonate-buffered solution. Recovery from an intracellular acid load brought about by the ammonium chloride pre-pulse technique was blocked by the removal of external sodium or the addition of 1.5 mM-amiloride, indicating the presence of a sodium-hydrogen exchange. 5. In bicarbonate-buffered solution pHi recovery after an acid load was also completely blocked by addition of 1.5 mM-amiloride indicating the absence of a bicarbonate-dependent acid extrusion mechanism. 6. Addition of 12-O-tetradecanoylphorbol-13-acetate (TPA, 100 nM) induced an amiloride-sensitive alkalinization of about 0.3 pH unit in bicarbonate-buffered solution but had no effect in HEPES-buffered solution. This observation suggests that in cultured Purkinje cells the sodium-hydrogen exchanger could be activated through a protein kinase C pathway only when pHi is maintained at a low physiological value by the activity of the chloride-bicarbonate exchange.
摘要
  1. 使用细胞内捕获的pH敏感染料2',7'-双-(2-羧乙基)-5(和-6)-羧基荧光素(BCECF)的显微光谱荧光分析,在原代培养的单个大鼠小脑浦肯野细胞中测量细胞内pH(pHi)。2. 使用K(+)-H+离子载体尼日利亚菌素校准在450和490nm交替激发下在530nm处测量的荧光信号的比率。当细胞在37℃下用5%CO2-25mM-HCO3(-)缓冲溶液在外部pH为7.40灌注时,该校准给出的稳态pHi为7.06±0.02(标准误,n = 17)。3. 在存在碳酸氢盐的情况下用葡萄糖酸盐替代外部氯化物会导致细胞质碱化约0.3个pH单位。这种碱化与外部钠无关,并且被0.5mM-DIDS大大降低,表明存在氯-碳酸氢盐交换。4. 在无碳酸氢盐(HEPES缓冲)溶液中,稳态pHi为7.37±0.02(n = 19),明显高于碳酸氢盐缓冲溶液。氯化铵预脉冲技术引起的细胞内酸负荷的恢复被去除外部钠或添加1.5mM氨氯吡脒所阻断,表明存在钠-氢交换。5. 在碳酸氢盐缓冲溶液中,酸负荷后的pHi恢复也被添加1.5mM氨氯吡脒完全阻断,表明不存在依赖碳酸氢盐的酸排出机制。6. 添加12-O-十四烷酰佛波醇-13-乙酸酯(TPA,100nM)在碳酸氢盐缓冲溶液中诱导约0.3个pH单位的氨氯吡脒敏感的碱化,但在HEPES缓冲溶液中没有作用。该观察结果表明,在培养的浦肯野细胞中,仅当通过氯-碳酸氢盐交换的活性将pHi维持在低生理值时,钠-氢交换体才能通过蛋白激酶C途径被激活。

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