Keith C, DiPaola M, Maxfield F R, Shelanski M L
J Cell Biol. 1983 Dec;97(6):1918-24. doi: 10.1083/jcb.97.6.1918.
The microinjection of calcium-saturated calmodulin into living fibroblasts causes the rapid disruption of microtubules and stress fibers in a sharply delimited region concentric with the injection site. This effect is specific to the calcium-bearing form of calmodulin; neither calcium-free calmodulin nor calcium ion at similar levels affects the cytoskeleton. If cells have previously been microinjected with calcium-free calmodulin, elevation of their intracellular calcium levels to 25 mM potentiates the disruption of microtubules throughout the cytoplasm. Approximately 400 mM free calcium is required to cause an equivalent disruption in uninjected cells. The level of calmodulin necessary to disrupt the full complement of cellular microtubules is found to be approximately in 2:1 molar ratio to tubulin dimer. These results indicate that calmodulin can be localized within the cytoplasm in a calcium-dependent manner and that it can act to regulate the calcium lability of microtubules at molar ratios that could be achieved locally within the cell. Our results are consistent with the hypothesis that calmodulin may be controlling microtubule polymerization equilibria in areas of high local concentration such as the mitotic spindle.
将钙饱和的钙调蛋白显微注射到活的成纤维细胞中,会导致在与注射部位同心的一个界限分明的区域内微管和应力纤维迅速破坏。这种效应是钙调蛋白的含钙形式所特有的;无钙的钙调蛋白或类似水平的钙离子均不影响细胞骨架。如果细胞先前已显微注射了无钙的钙调蛋白,将其细胞内钙水平提高到25 mM会增强整个细胞质中微管的破坏。在未注射的细胞中,大约需要400 mM的游离钙才能引起同等程度的破坏。发现破坏细胞微管全部成分所需的钙调蛋白水平与微管蛋白二聚体的摩尔比约为2:1。这些结果表明,钙调蛋白可以以钙依赖的方式定位于细胞质中,并且它可以在细胞内局部可达到的摩尔比下调节微管的钙敏感性。我们的结果与以下假设一致,即钙调蛋白可能在高局部浓度区域(如有丝分裂纺锤体)控制微管聚合平衡。