de Wit R J, Bulgakov R, Bominaar T A, Rinke de Wit T F
Biochim Biophys Acta. 1987 Aug 19;930(1):1-9. doi: 10.1016/0167-4889(87)90149-2.
The response of guanylate cyclase to addition of extracellular stimuli is well documented. Here we report for the first time the response of guanylate cyclase to removal of stimuli. Three methods were employed to terminate rapidly a stimulus of folic acid. (1) Addition of a highly active folate deaminase preparation, or (2) 12-fold dilution of the stimulated cell suspension, or (3) addition of an excess concentration of a non-agonistic derivative of folic acid, i.e., 2-deaminofolic acid, which chases the folate agonist from its cell-surface receptors. Accumulation of cGMP terminated instantaneously upon addition of deaminase, but degradation of the synthesized cGMP was not observed until 10-12 s after stimulation. Also in a cGMP phosphodiesterase-lacking 'streamer' mutant an instantaneous termination of further cGMP accumulation was observed upon stimulus removal. This suggests that the termination of cGMP accumulation is due to inactivation of guanylate cyclase instead of a steady state of cGMP synthesis and degradation. Further accumulation of cGMP was approx. 75% reduced upon dilution of a cell suspension after stimulation with both agonists. Stimulation by 300 nM folic acid or by 30 nM N10-methylfolic acid (a more potent agonist) yielded identical results. However, upon addition of deaminofolic acid the accumulation of cGMP continued normally if the cells had been stimulated with N10-methylfolic acid, but only slightly in the case of a folic acid stimulus. The effect of stimulus duration on desensitization was monitored; it was observed that 50% desensitization was induced by stimulation for 1 s, while 4 s was sufficient for maximal desensitization. Short stimuli were observed to elicit high levels of desensitization without much excitation of guanylate cyclase. A desensitization-like process was observed at the level of the folate-binding chemotactic receptors as well. Relationships between the cGMP response data and folic acid receptor kinetics are discussed.
鸟苷酸环化酶对细胞外刺激添加的反应已有充分记载。在此,我们首次报告鸟苷酸环化酶对刺激去除的反应。采用了三种方法来迅速终止叶酸刺激。(1)添加高活性叶酸脱氨酶制剂,或(2)将受刺激的细胞悬液稀释12倍,或(3)添加过量浓度的叶酸非激动剂衍生物,即2-脱氨叶酸,它从细胞表面受体上赶走叶酸激动剂。添加脱氨酶后,cGMP的积累立即终止,但直到刺激后10 - 12秒才观察到合成的cGMP降解。同样,在缺乏cGMP磷酸二酯酶的“拖尾”突变体中,刺激去除后也观察到cGMP进一步积累的立即终止。这表明cGMP积累的终止是由于鸟苷酸环化酶的失活,而不是cGMP合成与降解的稳态。刺激后用两种激动剂刺激细胞悬液稀释后,cGMP的进一步积累大约减少了75%。用300 nM叶酸或30 nM N10-甲基叶酸(一种更强效的激动剂)刺激产生了相同的结果。然而,添加脱氨叶酸后,如果细胞用N10-甲基叶酸刺激,cGMP的积累正常继续,但如果是叶酸刺激,则仅略有增加。监测了刺激持续时间对脱敏的影响;观察到刺激1秒诱导50%的脱敏,而4秒足以达到最大脱敏。观察到短时间刺激能引发高水平的脱敏,而鸟苷酸环化酶的激发不多。在叶酸结合趋化受体水平也观察到了类似脱敏的过程。讨论了cGMP反应数据与叶酸受体动力学之间的关系。