Thomason D B, Anderson O, Menon V
Department of Physiology and Biophysics, University of Tennessee, Health Science Center, Memphis 38163, USA.
J Appl Physiol (1985). 1996 Oct;81(4):1522-7. doi: 10.1152/jappl.1996.81.4.1522.
Head-down tilt by tail suspension of the rat produces a volume, but not pressure, load on the heart. One response of the heart is cytoskeleton rearrangement, a phenomenon commonly referred to as disruption. In these experiments, we used fractal analysis as a means to measure complexity of the microtubule structures at 8 and 18 h after imposition of head-down tilt. Microtubules in whole tissue cardiac myocytes were stained with fluorescein colchicine and were visualized by confocal microscopy. The fractal dimensions (D) of the structures were calculated by the dilation method, which involves successively dilating the outline perimeter of the microtubule structures and measuring the area enclosed. The head-down tilt resulted in a progressive decrease in D (decreased complexity) when measured at small dilations of the perimeter, but the maximum D (maximum complexity) of the microtubule structures did not change with treatment. Analysis of the fold change in complexity as a function of the dilation indicates an almost twofold decrease in microtubule complexity at small kernel dilations. This decrease in complexity is associated with a more Gaussian distribution of microtubule diameters, indicating a less structured microtubule cytoskeleton. We interpret these data as a microtubule rearrangement, rather than erosion, because total tubulin flourescence was not different between groups. This conclusion is supported by F-actin fluorescence data indicating a dispersed structure without loss of actin.
大鼠尾部悬吊引起的头低位倾斜会给心脏带来容量负荷而非压力负荷。心脏的一种反应是细胞骨架重排,这一现象通常被称为破坏。在这些实验中,我们使用分形分析来测量头低位倾斜8小时和18小时后微管结构的复杂性。全组织心肌细胞中的微管用荧光秋水仙碱染色,并通过共聚焦显微镜观察。结构的分形维数(D)通过扩张法计算,该方法包括依次扩张微管结构的轮廓周长并测量所包围的面积。当头低位倾斜时,在周长的小扩张时测量,D会逐渐降低(复杂性降低),但微管结构的最大D(最大复杂性)不会因处理而改变。将复杂性的倍数变化作为扩张的函数进行分析表明,在小内核扩张时微管复杂性几乎降低了两倍。这种复杂性的降低与微管直径更呈高斯分布有关,表明微管细胞骨架的结构较少。我们将这些数据解释为微管重排而非侵蚀,因为各组之间总微管蛋白荧光没有差异。F-肌动蛋白荧光数据表明结构分散但肌动蛋白没有损失,这支持了这一结论。