Cooper D M, Ahlijanian M K, Perez-Reyes E
Department of Pharmacology, University of Colorado Health Sciences Center, Denver 80262.
J Cell Biochem. 1988 Apr;36(4):417-27. doi: 10.1002/jcb.240360410.
Ca2+, through the mediation of calmodulin, stimulates the activity of brain adenylate cyclase. The growing awareness that fluctuating Ca2+ concentrations play a major role in intracellular signalling prompted the present study, which aimed to investigate the implications for neurotransmitter (receptor) regulation of enzymatic activity of this calmodulin regulation. The role of Ca2+/calmodulin in regulating neurotransmitter-mediated inhibition and stimulation was assessed in a number of rat brain areas. Ca2+/calmodulin stimulated adenylate cyclase activity in EGTA-washed plasma preparations from each region studied--from 1.3-fold (in striatum) to 3.4-fold (in cerebral cortex). The fold-stimulation produced by Ca2+/calmodulin was decreased in the presence of GTP, forskolin, or Mn2+. In EGTA-washed membranes, receptor-mediated inhibition of adenylate cyclase was strictly dependent upon Ca2+/calmodulin stimulation in all regions, except striatum. A requirement for Mg2+ in combination with Ca2+/calmodulin to observe neurotransmitter-mediated inhibition was also observed. In contrast, receptor-mediated stimulation of activity was much greater in the absence of Ca2+/calmodulin. The findings demonstrate that ambient Ca2+ concentrations, in concert with endogenous calmodulin, may play a central role in dictating whether inhibition or stimulation of adenylate cyclase by neurotransmitters may proceed.
钙离子通过钙调蛋白的介导,刺激脑腺苷酸环化酶的活性。人们越来越意识到,细胞内信号传导中钙离子浓度的波动起着主要作用,这促使了本研究的开展,其目的是研究这种钙调蛋白调节的酶活性对神经递质(受体)调节的影响。在多个大鼠脑区评估了钙离子/钙调蛋白在调节神经递质介导的抑制和刺激中的作用。钙离子/钙调蛋白刺激了所研究的每个区域经乙二醇双四乙酸(EGTA)洗涤的血浆制剂中的腺苷酸环化酶活性——从1.3倍(纹状体)到3.4倍(大脑皮层)。在存在鸟苷三磷酸(GTP)、福斯高林或锰离子(Mn2+)的情况下,钙离子/钙调蛋白产生的刺激倍数降低。在经EGTA洗涤的膜中,除纹状体外,所有区域中受体介导的腺苷酸环化酶抑制都严格依赖于钙离子/钙调蛋白刺激。还观察到,需要镁离子(Mg2+)与钙离子/钙调蛋白结合才能观察到神经递质介导的抑制。相比之下,在不存在钙离子/钙调蛋白的情况下,受体介导的活性刺激要大得多。这些发现表明,细胞外钙离子浓度与内源性钙调蛋白协同作用,可能在决定神经递质对腺苷酸环化酶的抑制或刺激是否能够发生方面发挥核心作用。