Harrison J K, Mickevicius C K, Gnegy M E
Department of Pharmacology, University of Michigan Medical School, Ann Arbor 48109-0010.
J Neurochem. 1988 Aug;51(2):345-52. doi: 10.1111/j.1471-4159.1988.tb01045.x.
The concentration requirements of calmodulin in altering basal, GTP-, and dopamine-stimulated adenylate cyclase activities in an EGTA-washed particulate fraction from bovine striatum were examined. In the bovine striatal particulate fraction, calmodulin activated basal adenylate cyclase activity 3.5-fold, with an EC50 of 110 nM. Calmodulin also potentiated the activation of adenylate cyclase by GTP by decreasing the EC50 for GTP from 303 +/- 56 nM to 60 +/- 10 nM. Calmodulin did not alter the maximal response to GTP. The EC50 for calmodulin in potentiating the GTP response was only 11 nM as compared to 110 nM for activation of basal activity. Similarly, calmodulin increased the maximal stimulation of adenylate cyclase by dopamine by 50-60%. The EC50 for calmodulin in eliciting this response was 35 nM. These data demonstrate that calmodulin can both activate basal adenylate cyclase and potentiate adenylate cyclase activities that involve the activating GTP-binding protein, Ns. Mechanisms that involve potentiation of Ns-mediated effects are much more sensitive to calmodulin than is the activation of basal adenylate cyclase activity. Potentiation of GTP-stimulated adenylate cyclase activity by calmodulin was apparent at 3 and 5 mM MgCl2, but not at 1 or 10 mM MgCl2. These data further support a role for calmodulin in hormonal signalling and suggest that calmodulin can regulate cyclic AMP formation by more than one mechanism.
研究了钙调蛋白在改变来自牛纹状体的经乙二醇双(2-氨基乙基醚)四乙酸(EGTA)洗涤的微粒体部分中基础、GTP和多巴胺刺激的腺苷酸环化酶活性时的浓度需求。在牛纹状体微粒体部分中,钙调蛋白使基础腺苷酸环化酶活性激活3.5倍,半数有效浓度(EC50)为110 nM。钙调蛋白还通过将GTP的EC50从303±56 nM降低至60±10 nM来增强GTP对腺苷酸环化酶的激活作用。钙调蛋白未改变对GTP的最大反应。与激活基础活性的110 nM相比,钙调蛋白增强GTP反应的EC50仅为11 nM。同样,钙调蛋白使多巴胺对腺苷酸环化酶的最大刺激增加50 - 60%。引发此反应的钙调蛋白的EC50为35 nM。这些数据表明钙调蛋白既能激活基础腺苷酸环化酶,又能增强涉及激活型GTP结合蛋白Ns的腺苷酸环化酶活性。涉及增强Ns介导作用的机制对钙调蛋白比基础腺苷酸环化酶活性的激活更敏感。在3 mM和5 mM氯化镁(MgCl2)时,钙调蛋白对GTP刺激的腺苷酸环化酶活性的增强作用明显,但在1 mM或10 mM MgCl2时则不明显。这些数据进一步支持了钙调蛋白在激素信号传导中的作用,并表明钙调蛋白可通过多种机制调节环磷酸腺苷(cAMP)的形成。