Ho C L, Martys J L, Mikhailov A, Gundersen G G, Liem R K
Department of Pathology, Columbia University College of Physicians and Surgeons, New York, New York 10032, USA.
J Cell Sci. 1998 Jul;111 ( Pt 13):1767-78. doi: 10.1242/jcs.111.13.1767.
In order to study the dynamic behavior of intermediate filament networks in living cells, we have prepared constructs fusing green fluorescent protein to intermediate filament proteins. Vimentin fused to green fluorescent protein labeled the endogenous intermediate filament network. We generated stable SW13 and NIH3T3 cell lines that express an enhanced green fluorescent protein fused to the N-terminus of full-length vimentin. We were able to observe the dynamic behavior of the intermediate filament network in these cells for periods as long as 4 hours (images acquired every 2 minutes). In both cell lines, the vimentin network constantly moves in a wavy manner. In the NIH3T3 cells, we observed extension of individual vimentin filaments at the edge of the cell. This movement is dependent on microtubules, since the addition of nocodazole stopped the extension of the intermediate filaments. Injection of anti-IFA causes the redistribution or 'collapse' of intermediate filaments. We injected anti-IFA antibodies into NIH3T3 cells stably expressing green fluorescent protein fused to vimentin and found that individual intermediate filaments move slowly towards the perinuclear area without obvious disassembly. These results demonstrate that individual intermediate filaments are translocated during the collapse, rather than undergoing disassembly-induced redistribution. Injections of tubulin antibodies disrupt the interactions between intermediate filaments and stable microtubules and cause the collapse of the vimentin network showing that these interactions play an important role in keeping the intermediate filament network extended. The nocodazole inhibition of intermediate filament extension and the anti-IFA microinjection experiments are consistent with a model in which intermediate filaments exhibit an extended distribution when tethered to microtubules, but are translocated to the perinuclear area when these connections are severed.
为了研究活细胞中中间丝网络的动态行为,我们制备了将绿色荧光蛋白与中间丝蛋白融合的构建体。与绿色荧光蛋白融合的波形蛋白标记了内源性中间丝网络。我们生成了稳定表达与全长波形蛋白N端融合的增强型绿色荧光蛋白的SW13和NIH3T3细胞系。我们能够在长达4小时的时间内观察这些细胞中中间丝网络的动态行为(每2分钟采集一次图像)。在这两种细胞系中,波形蛋白网络持续以波浪状移动。在NIH3T3细胞中,我们观察到单个波形蛋白丝在细胞边缘延伸。这种移动依赖于微管,因为加入诺考达唑会阻止中间丝的延伸。注射抗中间丝自身抗体导致中间丝重新分布或“塌陷”。我们将抗中间丝自身抗体注射到稳定表达与波形蛋白融合的绿色荧光蛋白的NIH3T3细胞中,发现单个中间丝缓慢移向核周区域,且无明显解聚。这些结果表明,在塌陷过程中单个中间丝发生了移位,而不是经历由解聚引起的重新分布。注射微管蛋白抗体破坏了中间丝与稳定微管之间的相互作用,并导致波形蛋白网络塌陷,表明这些相互作用在维持中间丝网络伸展方面起重要作用。诺考达唑对中间丝延伸的抑制以及抗中间丝自身抗体显微注射实验与一个模型相符,即当中间丝与微管相连时呈现伸展分布,但当这些连接被切断时会移位到核周区域。