Adler M, Sabol S L, Busis N, Pant H C
Neurotoxicology Branch, US Army Medical Research Institute of Chemical Defense, Aberdeen Proving Ground, Maryland.
Cell Calcium. 1989 Oct;10(7):467-76. doi: 10.1016/0143-4160(89)90024-9.
Intracellular ionized Ca2+ concentration was measured in clonal mouse anterior pituitary tumor cells with the fluorescent Ca2+ indicator Quin-2. In control physiological solution, free cytoplasmic Ca2+ concentration was found to be 139 +/- 11 nM. Replacement of 50 mM NaCl by 50 mM KCl in the extracellular fluid caused a 29 mV depolarization and a 4.2-fold increase in the concentration of free cytoplasmic Ca2+. Under comparable depolarizing conditions, a specific influx of 2.66 nmole of 45Ca2+ per mg protein was detected 1 min after addition of high K+, accompanied by a marked increase in the initial rate of beta-endorphin secretion. In the absence of external Ca2+, depolarization by K+ produced little or no increase in either intracellular free Ca2+ or hormone release. Incubation of AtT-20/D16-16 cells in the secretagogue norepinephrine led to a depolarization accompanied by an increase in spontaneous action potential frequency and a marked elevation in cytosolic Ca2+ concentration. Exposure of cells to somatostatin, an inhibitor of hormone release, led to only transient decreases in burst frequency and no significant reduction in intracellular Ca2+ levels. These results indicate that in addition to intracellular Ca2+, other factors also control secretory activity in AtT-20/D16-16 anterior pituitary cells.
采用荧光钙指示剂喹啉-2,测定克隆的小鼠垂体前叶肿瘤细胞内的游离钙离子浓度。在对照生理溶液中,发现游离细胞质钙离子浓度为139±11 nM。细胞外液中用50 mM KCl替代50 mM NaCl,导致去极化29 mV,游离细胞质钙离子浓度增加4.2倍。在类似的去极化条件下,加入高钾后1分钟,检测到每毫克蛋白质有2.66 nmol的45Ca2+特异性内流,同时β-内啡肽分泌的初始速率显著增加。在无细胞外钙离子的情况下,钾离子去极化对细胞内游离钙离子或激素释放几乎没有影响。将AtT-20/D16-16细胞置于促分泌剂去甲肾上腺素中孵育,导致去极化,同时自发动作电位频率增加,细胞质钙离子浓度显著升高。将细胞暴露于激素释放抑制剂生长抑素中,仅导致爆发频率短暂降低,细胞内钙离子水平无显著降低。这些结果表明,除了细胞内钙离子外,其他因素也控制AtT-20/D16-16垂体前叶细胞的分泌活动。