Blose S H
Cell Motil. 1981;1(4):417-31. doi: 10.1002/cm.970010403.
I have used fluorescence microscopy and antibodies to 10nm filaments and tubulin labelled with contrasting fluorochromes to compare the distribution of these proteins in endothelial cells during cell division. During interphase the two filament systems have entirely different distributions: The bulk of the 10nm filaments form a ring that surrounds the cell center and nucleus and remains parallel to the substrate, while the microtubules radiate from the cell center to the cell's border. When the mitotic spindle replaces the radial microtubule pattern in mitosis, the spindle poles remain within--and in close proximity to--the ring of 10nm filaments. This was confirmed by electron microscopy which showed the ring and centrioles in the same plane separated by a distance of 300-400 nm.
我使用荧光显微镜以及针对10纳米细丝和用对比荧光染料标记的微管蛋白的抗体,来比较这些蛋白质在细胞分裂期间在内皮细胞中的分布情况。在间期,这两种细丝系统具有完全不同的分布:大部分10纳米细丝形成一个环绕细胞中心和细胞核的环,并与底物保持平行,而微管则从细胞中心向细胞边缘辐射。当有丝分裂纺锤体在有丝分裂中取代放射状微管模式时,纺锤体极仍位于10纳米细丝环内并与之紧密相邻。电子显微镜证实了这一点,其显示环和中心粒在同一平面,相距300 - 400纳米。