Wang E, Cross R K, Choppin P W
J Cell Biol. 1979 Nov;83(2 Pt 1):320-37. doi: 10.1083/jcb.83.2.320.
Previous studies (Holmes, K.V., and P.W. Choppin. J. Exp. Med. 124:501-520; J. Cell Biol. 39:526-543) showed that infection of baby hamster kidney (BHK21-F) cells with the parainfluenza virus SV5 causes extensive cell fusion, that nuclei migrate in the syncytial cytoplasm and align in tightly-packed rows, and that microtubules are involved in nuclear movement and alignment. The role of microtubules, 10-nm filaments, and actin-containing microfilaments in this process has been investigated by immunofluorescence microscopy using specific antisera, time-lapse cinematography, and electron microscopy. During cell fusion, micro tubules and 10-nm filaments from many cells form large bundles which are localized between rows of nuclei. No organized bundles of actin fibers were detected in these areas, although actin fibers were observed in regions away from the aligned nuclei. Although colchicine disrupts microtubules and inhibits nuclear movement, cytochalasin B (CB; 20-50 microgram/ml) does not inhibit cell fusion or nuclear movement. However, CB alters the shape of the syncytium, resulting in long filamentous processes extending from a central region. When these processes from neighboring cells make contact, fusion occurs, and nuclei migrate through the channels which are formed. Electron and immunofluorescence microscopy reveal bundles of microtubules and 10-nm filaments in parallel arrays within these processes, but no bundles of microfilaments were detected. The effect of CB on the structural integrity of microfilaments at this high concentration (20 microgram/ml) was demonstrated by the disappearance of filaments interacting with heavy meromyosin. Cycloheximide (20 microgram/ml) inhibits protein synthesis but does not affect cell fusion, the formation of microtubules and 10-nm filament bundles, or nuclear migration and alignment; thus, continued protein synthesis is not required. The association of microtubules and 10-nm filaments with nuclear migration and alignment suggests that microtubules and 10-nm filaments are two components in a system which serves both cytoskeletal and force-generating functions in intracellular movement and position of nuclei.
先前的研究(霍姆斯,K.V.,以及P.W. 乔平。《实验医学杂志》124:501 - 520;《细胞生物学杂志》39:526 - 543)表明,用副流感病毒SV5感染幼仓鼠肾(BHK21 - F)细胞会导致广泛的细胞融合,细胞核在多核体细胞质中迁移并排列成紧密堆积的行,并且微管参与细胞核的移动和排列。在此过程中,微管、10纳米细丝和含肌动蛋白的微丝的作用已通过使用特异性抗血清的免疫荧光显微镜检查、延时电影摄影术和电子显微镜进行了研究。在细胞融合过程中,来自许多细胞的微管和10纳米细丝形成大的束,这些束位于细胞核行之间。在这些区域未检测到有组织的肌动蛋白纤维束,尽管在远离排列好的细胞核的区域观察到了肌动蛋白纤维。虽然秋水仙碱会破坏微管并抑制细胞核移动,但细胞松弛素B(CB;20 - 50微克/毫升)并不抑制细胞融合或细胞核移动。然而,CB会改变多核体的形状,导致从中心区域延伸出长丝状突起。当相邻细胞的这些突起接触时,就会发生融合,细胞核通过形成的通道迁移。电子显微镜和免疫荧光显微镜显示,在这些突起内,微管和10纳米细丝束呈平行排列,但未检测到微丝束。在这种高浓度(20微克/毫升)下,CB对微丝结构完整性的影响通过与重酶解肌球蛋白相互作用的细丝消失得以证明。放线菌酮(20微克/毫升)抑制蛋白质合成,但不影响细胞融合、微管和10纳米细丝束的形成,或细胞核的迁移和排列;因此,不需要持续的蛋白质合成。微管和10纳米细丝与细胞核迁移和排列的关联表明,微管和10纳米细丝是一个系统中的两个组成部分,该系统在细胞核的细胞内移动和定位中兼具细胞骨架和产生力的功能。