Clyne J D, Brown T C, Hume R I
Department of Molecular, Cellular, and Developmental Biology, University of Michigan, 3095 Natural Science Building, 830 N. University Avenue, Ann Arbor, MI 48109-1048, USA.
Neuropharmacology. 2003 Mar;44(3):403-12. doi: 10.1016/s0028-3908(02)00406-9.
The currents of P2X(2) receptors expressed in Xenopus oocytes or HEK293 cells show significant cell-to-cell variation in many properties including the rate of desensitization and the magnitude of potentiation by zinc or acidic pH. In this study, we examined whether differences in expression levels underlie this variability. We injected Xenopus oocytes with different concentrations of RNA encoding rat P2X(2) to give a wide range of maximum current amplitudes, and then measured the potentiation of responses to 10 micro M adenosine 5'-triphosphate (ATP) by zinc or acidic pH. Individual oocytes showed potentiation ratios that ranged from 1.4- to 25-fold. Oocytes with small amplitude responses to a saturating concentration of ATP tended to have larger potentiation ratios than oocytes with large amplitude responses. This phenomenon was explained by an inverse correlation between the EC(50) for ATP and the maximum current amplitude, with the EC(50) decreasing from about 37 to 7 micro M as expression level increased. In contrast, the Hill coefficient was not correlated with the maximum current amplitude. Truncated receptors lacking the last 76 amino acids also showed an inverse correlation between the EC(50) and the maximum current amplitude. Thus, the interactions that cause expression-dependent changes in P2X(2) receptor properties must involve domains proximal to position H397.
在非洲爪蟾卵母细胞或人胚肾293(HEK293)细胞中表达的P2X(2)受体电流,在包括脱敏速率以及锌或酸性pH值增强幅度等许多特性方面,表现出显著的细胞间差异。在本研究中,我们检测了表达水平的差异是否是这种变异性的基础。我们向非洲爪蟾卵母细胞注射不同浓度的编码大鼠P2X(2)的RNA,以产生广泛范围的最大电流幅度,然后测量锌或酸性pH值对10微摩尔5'-三磷酸腺苷(ATP)反应的增强作用。单个卵母细胞的增强比范围为1.4至25倍。对饱和浓度ATP反应幅度小的卵母细胞,其增强比往往比反应幅度大的卵母细胞更大。这一现象可通过ATP的半数有效浓度(EC(50))与最大电流幅度之间的负相关来解释,随着表达水平增加,EC(50)从约37微摩尔降至7微摩尔。相比之下,希尔系数与最大电流幅度无关。缺失最后76个氨基酸的截短型受体,其EC(50)与最大电流幅度之间也呈负相关。因此,导致P2X(2)受体特性发生表达依赖性变化的相互作用,必定涉及靠近H397位置的结构域。