Titievsky A V, Takeo T, Tepikin A V, Petersen O H
MRC Secretory Control Research Group, Physiological Laboratory, University of Liverpool, Liverpool, L69 3BX, UK.
Pflugers Arch. 1996 Sep;432(5):938-40. doi: 10.1007/s004240050218.
In isolated pancreatic acinar cells application of the proton-potassium ionophore nigericin or the proton-sodium ionophore monensin led to a reduction of acidity inside the zymogen granules which could be visualized in an imaging system by a rapid reduction in the intragranular quinacrine fluorescence. Cytosolic Ca2+ spikes in response to acetylcholine stimulation or intracellular inositol trisphosphate application were assessed by recording Ca2+ -sensitive ionic currents in the patch clamp whole-cell recording configuration. Both nigericin and monensin evoked marked reductions in frequency and amplitude of spikes and in many experiments abolished spiking altogether. The Ca2+ -sensitive membrane currents could still be activated after nigericin or monensin treatment since subsequent application of the Ca2+ ionophore ionomycin evoked a large current response. The decrease in intragranular acidity would appear to inhibit intracellular Ca2+ release perhaps due to a reduction in the free intragranular Ca2+ concentration.
在分离的胰腺腺泡细胞中,应用质子 - 钾离子载体尼日利亚菌素或质子 - 钠离子载体莫能菌素会导致酶原颗粒内酸度降低,这在成像系统中可通过颗粒内喹吖因荧光的快速减弱来观察到。通过在膜片钳全细胞记录模式下记录钙敏感离子电流,评估了对乙酰胆碱刺激或细胞内肌醇三磷酸应用的细胞溶质Ca²⁺ 尖峰。尼日利亚菌素和莫能菌素均引起尖峰频率和幅度的显著降低,并且在许多实验中完全消除了尖峰现象。在尼日利亚菌素或莫能菌素处理后,钙敏感膜电流仍可被激活,因为随后应用钙离子载体离子霉素会引发大的电流反应。颗粒内酸度的降低似乎会抑制细胞内Ca²⁺ 的释放,这可能是由于颗粒内游离Ca²⁺ 浓度降低所致。