Van Haastert P J
J Biol Chem. 1987 Jun 5;262(16):7700-4.
cAMP binds to Dictyostelium discoideum surface receptors and induces a transient activation of adenylatecyclase, which is followed by desensitization. cAMP also induces a loss of detectable surface receptors (down-regulation). Cells were incubated with constant cAMP concentrations, washed free of cAMP, and cAMP binding to surface receptors and cAMP-induced activation of adenylate cyclase were measured. cAMP could induce maximally 65% loss of binding activity and complete desensitization of cAMP-stimulated adenylate cyclase activity. Half-maximal effects for down-regulation were observed at 50 nM cAMP and for desensitization at 5 nM cAMP. Down-regulation was rapid with half-times of 4, 2.5, and 1 min at 0.1, 1, and 10 microM cAMP, respectively. Similar kinetic data have been reported for desensitization (Dinauer, M.C., Steck, T.L., and Devreotes, P.N. (1980) J. Cell Biol. 86, 554-561). Down-regulation and desensitization were not reversible at 0 degrees C. Down-regulation reversed slowly at 20 degrees C with a half-time of about 1 h. Resensitization of adenylate cyclase was biphasic showing half-times of 4 min and about 1 h, respectively; the contribution of the rapidly resensitizing component was diminished when down-regulation of receptors was enhanced. These results suggest that cAMP-induced down-regulation of receptors and desensitization of adenylate cyclase stimulation proceed by at least two steps. One step is rapidly reversible, occurs at low cAMP concentrations, and induces desensitization without down-regulation, while the second step is slowly reversible, requires higher cAMP concentrations, and also induces down-regulation.
环磷酸腺苷(cAMP)与盘基网柄菌表面受体结合,诱导腺苷酸环化酶短暂激活,随后发生脱敏。cAMP还会导致可检测到的表面受体丧失(下调)。将细胞与恒定浓度的cAMP孵育,洗去cAMP,然后测量cAMP与表面受体的结合以及cAMP诱导的腺苷酸环化酶激活。cAMP可最大程度地诱导65%的结合活性丧失,并使cAMP刺激的腺苷酸环化酶活性完全脱敏。下调的半数最大效应在50 nM cAMP时观察到,脱敏的半数最大效应在5 nM cAMP时观察到。下调迅速,在0.1、1和10 μM cAMP时的半衰期分别为4、2.5和1分钟。关于脱敏也报道了类似的动力学数据(迪瑙尔,M.C.,斯特克,T.L.,和德夫罗茨,P.N.(1980年)《细胞生物学杂志》86,554 - 561)。在0℃时,下调和脱敏是不可逆的。在20℃时,下调缓慢逆转,半衰期约为1小时。腺苷酸环化酶的再敏化是双相的,半衰期分别为4分钟和约1小时;当受体下调增强时,快速再敏化成分的贡献会减少。这些结果表明,cAMP诱导的受体下调和腺苷酸环化酶刺激的脱敏至少通过两个步骤进行。一个步骤是快速可逆的,发生在低cAMP浓度下,诱导脱敏而不下调,而第二个步骤是缓慢可逆的,需要更高的cAMP浓度,并且还诱导下调。