Stoop R, Quayle J M
Geneva Biomedical Research Institute, Glaxo-Wellcome Research and Development, Geneva, Switzerland.
Br J Pharmacol. 1998 Sep;125(2):235-7. doi: 10.1038/sj.bjp.0702056.
When ATP is applied at high concentrations (above 1 mM) to PC12 cells, it produces a rapidly desensitizing peak current followed by a rebound of the current after termination of the ATP application. We expressed P2X2 receptors, which are thought to mediate the ATP currents of PC12 cells, in HEK293 cells and studied the effects of acidification on this 'fading and rebound' phenomenon. We found that the desensitization disappeared after adjusting the low pH (<5.0) of the millimolar ATP concentrations to a more physiological value (pH 7.3). Furthermore, the fading and rebound could also be induced at much lower ATP concentrations by decreasing the pH of the ATP containing application solutions. Thus, it appears this phenomenon is not caused directly by high concentrations of ATP, but is due to a concomitant acidification that occurs when high concentrations of ATP are dissolved in only moderately buffered application solutions.
当以高浓度(高于1 mM)将ATP应用于PC12细胞时,会产生一个快速脱敏的峰值电流,在ATP应用终止后电流会出现反弹。我们在HEK293细胞中表达了被认为介导PC12细胞ATP电流的P2X2受体,并研究了酸化对这种“衰减和反弹”现象的影响。我们发现,将毫摩尔ATP浓度的低pH值(<5.0)调整到更接近生理值(pH 7.3)后,脱敏现象消失。此外,通过降低含ATP应用溶液的pH值,在低得多的ATP浓度下也能诱导衰减和反弹。因此,看来这种现象不是由高浓度的ATP直接引起的,而是由于当高浓度的ATP溶解在缓冲程度适中的应用溶液中时伴随出现的酸化所致。