Hesketh T R, Smith G A, Moore J P, Taylor M V, Metcalfe J C
J Biol Chem. 1983 Apr 25;258(8):4876-82.
The effects of the lectins concanavalin A, succinylated concanavalin A, and wheat germ agglutinin on the free cytoplasmic Ca2+ concentration in mouse thymocytes were measured using the fluorescent Ca2+ indicator "quin 2" (Tsien, R. Y. (1980) Biochemistry 19, 2396-2404) and compared with the metabolic and mitogenic effects of the lectins on the cells. Within 1 min of adding each ligand, there is a dose-dependent increase in the free cytoplasmic Ca2+ concentration reported by quin 2. This response is selective for Ca2+, but it does not coincide closely with the subsequent mitogenic stimulation at 48 h by concanavalin A or succinyl concanavalin A. The nonmitogenic lectin wheat germ agglutinin also causes an increase in free cytoplasmic Ca2+ concentration and early metabolic stimulation of the cells, but stimulation is self-aborted before DNA synthesis occurs. At the intracellular concentrations of quin 2 required for measurement of the free Ca2+ concentration, the chelator causes early metabolic stimulation of the cells very similar to that produced by concanavalin A and the mitogenic Ca2+ ionophore A23187. Thus, phosphatidylinositol metabolism and lactate production are stimulated in mouse thymocytes and pig lymphocytes within 1 h of loading with quin 2 and significant increases in RNA synthesis occur after 8 h. Quin 2 causes mitogenic stimulation of pig lymphocytes measured as increased [3H]thymidine uptake at 48 h, that is variable but substantial in most experiments (up to 100% of the stimulation by A23187). The chelator itself has no significant activity as a Ca2+ ionophore, but the apparent free Ca2+ concentration in the cells increases both with the concentration of intracellular quin 2 and with the extracellular Ca2+ concentration. These data leave open the possibility that quin 2 itself affects the concentration of free Ca2+ or other cations in the cells.
使用荧光钙指示剂“喹啉2”(钱永佑,R.Y.(1980年)《生物化学》19卷,2396 - 2404页)测定了伴刀豆球蛋白A、琥珀酰化伴刀豆球蛋白A和麦胚凝集素对小鼠胸腺细胞中游离细胞质钙离子浓度的影响,并将其与这些凝集素对细胞的代谢和促有丝分裂作用进行了比较。在添加每种配体后的1分钟内,喹啉2报告的游离细胞质钙离子浓度呈剂量依赖性增加。这种反应对钙离子具有选择性,但与伴刀豆球蛋白A或琥珀酰伴刀豆球蛋白A在48小时后随后的促有丝分裂刺激并不紧密一致。无促有丝分裂活性的凝集素麦胚凝集素也会导致游离细胞质钙离子浓度增加以及细胞的早期代谢刺激,但在DNA合成发生之前刺激就自行终止了。在测量游离钙离子浓度所需的喹啉2细胞内浓度下,该螯合剂会引起细胞的早期代谢刺激,与伴刀豆球蛋白A和促有丝分裂钙离子载体A23187所产生的刺激非常相似。因此,在加载喹啉2的1小时内,小鼠胸腺细胞和猪淋巴细胞中的磷脂酰肌醇代谢和乳酸生成受到刺激,8小时后RNA合成显著增加。喹啉2会引起猪淋巴细胞的促有丝分裂刺激,以48小时时[³H]胸腺嘧啶核苷摄取增加来衡量,在大多数实验中这种刺激是可变的但很显著(高达A23187刺激的100%)。该螯合剂本身作为钙离子载体没有显著活性,但细胞内的表观游离钙离子浓度会随着细胞内喹啉2的浓度以及细胞外钙离子浓度的增加而增加。这些数据留下了喹啉2本身影响细胞内游离钙离子或其他阳离子浓度的可能性。