Carter T D, Ogden D
Division of Neurophysiology and Neuropharmacology, National Institute for Medical Research, Mill Hill, London, U.K.
Proc Biol Sci. 1992 Dec 22;250(1329):235-41. doi: 10.1098/rspb.1992.0154.
Quantitative, time-resolved measurements have been made of intracellular Ca ion release by inositol 1,4,5-trisphosphate (InsP3) and extracellular ATP in porcine aortic endothelial cells in tissue culture. Intracellular free [Ca] was detected with the calcium dye fluo-3 and InsP3 released intracellularly by photolysis of 'caged' InsP3 in whole-cell voltage-clamped aortic endothelial cells. A rise of [Ca] was recorded at InsP3 concentrations greater than 0.2 microM. The timecourse at low InsP3 concentrations comprised a delay of mean 300 ms (range 266-330 ms), a peak in 2-3 s before declining with a half-time of 5-10 s. The delay and time-to-peak decreased with increasing concentrations of InsP3 over the range 0.2-5 microM. At very high concentrations of InsP3 (> 5 microM), the delay in the Ca response was short, always less than 20 ms. The results are consistent with a direct binding and gating action of InsP3 on the Ca channel of the cellular store. Following InsP3 action there is a refractoriness of the InsP3 Ca release process which recovers with a timecourse of half-time about 30 s. A comparison can be made between the timecourse of InsP3 and extracellular ATP actions. High concentrations of ATP (500 microM) acted with a delay of mean 1.8 s (range 1.2-2.5 s), whereas even moderate concentrations of InsP3 acted much more quickly, suggesting that there are slow coupling steps before or during the production of InsP3 in response to extracellular ATP. Both ATP and InsP3 evoked an increase in membrane conductance to K+, probably via Ca.
对组织培养的猪主动脉内皮细胞中,由肌醇1,4,5 -三磷酸(InsP3)和细胞外ATP引发的细胞内钙离子释放进行了定量的、时间分辨测量。在全细胞膜片钳的主动脉内皮细胞中,用钙染料Fluo - 3检测细胞内游离钙离子浓度,并通过“笼化”InsP3的光解来释放细胞内的InsP3。当InsP3浓度大于0.2微摩尔时,记录到钙离子浓度升高。低InsP3浓度下的时间进程包括平均300毫秒的延迟(范围为266 - 330毫秒),在2 - 3秒达到峰值,随后以5 - 10秒的半衰期下降。在0.2 - 5微摩尔范围内,随着InsP3浓度增加,延迟和达到峰值的时间减少。在非常高的InsP3浓度(>5微摩尔)下,钙离子反应的延迟很短,总是小于20毫秒。这些结果与InsP3对细胞内钙库钙通道的直接结合和门控作用一致。InsP3作用后,InsP3钙释放过程存在不应期,其恢复的半衰期约为30秒。可以对InsP3和细胞外ATP作用时间进程进行比较。高浓度的ATP(500微摩尔)作用时平均延迟1.8秒(范围为1.2 - 2.5秒),而即使是中等浓度的InsP3作用也快得多,这表明在响应细胞外ATP产生InsP3之前或过程中存在缓慢的偶联步骤。ATP和InsP3都引起细胞膜对钾离子的电导增加,可能是通过钙离子介导的。