Chamberlain L H, Roth D, Morgan A, Burgoyne R D
Physiological Laboratory, University of Liverpool, United Kingdom.
J Cell Biol. 1995 Sep;130(5):1063-70. doi: 10.1083/jcb.130.5.1063.
We have used stage-specific assays for MgATP-dependent priming and for Ca(2+)-activated triggering in the absence of free MgATP to examine the effects of alpha-SNAP, 14-3-3 proteins and calmodulin on regulated exocytosis in permeabilized adrenal chromaffin cells. All three proteins lead to a Ca(2+)-dependent increase in catecholamine secretion. Both alpha-SNAP and 14-3-3 proteins stimulated in a priming but not in a triggering assay. In contrast, calmodulin was stimulatory in triggering but not priming. The effects of alpha-SNAP and 14-3-3 proteins were likely to be due to distinct mechanisms of action since they differed in Ca(2+)-dependency, time course and extent of stimulation and their effects were additive. alpha-SNAP and 14-3-3 proteins did not appear to exert their priming action through changes in synthesis of phosphatidylinositol (4,5) bisphosphate. The data show that these three proteins have distinct stage-specific actions on exocytosis and indicate that alpha-SNAP acts in an early MgATP-requiring stage and not in the late Ca(2+)-triggered steps immediately prior to membrane fusion as previously suggested.
我们利用特定阶段的检测方法,分别检测了在无游离MgATP情况下MgATP依赖的引发作用以及Ca(2+)激活的触发作用,以此来研究α-SNAP、14-3-3蛋白和钙调蛋白对通透化肾上腺嗜铬细胞中调节性胞吐作用的影响。这三种蛋白均导致儿茶酚胺分泌呈Ca(2+)依赖性增加。α-SNAP和14-3-3蛋白在引发检测中具有刺激作用,但在触发检测中无此作用。相比之下,钙调蛋白在触发检测中有刺激作用,而在引发检测中无此作用。α-SNAP和14-3-3蛋白的作用可能归因于不同的作用机制,因为它们在Ca(2+)依赖性、时间进程和刺激程度上存在差异,且它们的作用具有加和性。α-SNAP和14-3-3蛋白似乎并非通过改变磷脂酰肌醇(4,5)二磷酸的合成来发挥其引发作用。数据表明,这三种蛋白对胞吐作用具有不同的阶段特异性作用,并表明α-SNAP在早期需要MgATP的阶段发挥作用,而不是如先前推测的那样在紧接膜融合之前的晚期Ca(2+)触发步骤中发挥作用。