Grosman N
Department of Pharmacology, University of Copenhagen, Denmark.
Agents Actions. 1992 Jul;36(3-4):192-9.
Investigations of calmodulin involvement in cell responses has been complicated by the lack of selective calmodulin antagonists. A novel inhibitor, CGS 9343B, reportedly without influence on protein kinase C, is used in the present study of mast cell responses. The histamine release induced by antigen and compound 48/80 in the presence of calcium was enhanced by 10-20 microM CGS 9343B and inhibited by higher concentrations. Only inhibitory effects on the response to compound 48/80 in the absence of calcium and to the ionophore A23187 were observed, the latter being inhibited by 20 microM CGS 9343B. The influence on responses to combinations of the phorbol ester TPA and the ionophore A23187 was more complex, giving rise to enhancement at lower and inhibition at higher concentrations of CGS 9343B in a manner which depended on the experimental conditions. Unlike previously used calmodulin antagonists, CGS 9343B is devoid of detergent effects and without serious metabolic interference. The inhibitor seems useful to reveal differences in the mechanisms involved in responses to various histamine liberators. Our results conform with an inhibition of calmodulin by CGS 9343B but are at present inconclusive.
由于缺乏选择性钙调蛋白拮抗剂,对钙调蛋白参与细胞反应的研究变得复杂。一种新型抑制剂CGS 9343B,据报道对蛋白激酶C没有影响,被用于本肥大细胞反应的研究中。在有钙存在的情况下,10 - 20微摩尔的CGS 9343B可增强抗原和化合物48/80诱导的组胺释放,而更高浓度则起抑制作用。仅观察到在无钙情况下对化合物48/80反应以及对离子载体A23187反应的抑制作用,后者可被20微摩尔的CGS 9343B抑制。对佛波酯TPA和离子载体A23187组合反应的影响更为复杂,在较低浓度的CGS 9343B下产生增强作用,在较高浓度下产生抑制作用,其方式取决于实验条件。与先前使用的钙调蛋白拮抗剂不同,CGS 9343B没有去污剂效应且没有严重的代谢干扰。该抑制剂似乎有助于揭示对各种组胺释放剂反应所涉及机制的差异。我们的结果符合CGS 9343B对钙调蛋白的抑制作用,但目前尚无定论。