Hayden J H, Allen R D, Goldman R D
Cell Motil. 1983;3(1):1-19. doi: 10.1002/cm.970030102.
We report the first direct demonstration that the cytoplasmic transport of organelles and vesicles (collectively called particles) takes place along microtubules. Living keratocytes from the corneal stroma of the frog, Rana pipiens were observed with Allen video-enhanced contrast, differential interference contrast (AVEC-DIC) microscopy [Allen et al, 1981]. In sufficiently thin regions of these cells a network of linear elements was visible. When particles were observed in motion, they always moved along these linear elements. The linear elements remained intact and in focus on the microscope when lysed in a cell lysis solution that stabilized microtubules. Preparations were then fixed in formaldehyde, washed with phosphate-buffered saline (PBS), incubated with rabbit antitubulin, washed with PBS, stained with rhodamine-conjugated goat antirabbit, and washed with PBS. The extracted cells continued to remain in place and in focus on the microscope throughout these procedures. The same cells were then observed using epifluorescence optics and a silicon-intensified target (SIT) video camera. A network of fluorescent linear elements was seen to correspond in number, form, and position to the linear elements seen in the live AVEC-DIC image. Taken together, the AVEC-DIC and fluorescence microscopy observations prove that the linear elements along which particles move are microtubules (MTLEs). The observed particle speeds, pause times, and distances moved varied widely, even for the same particle on the same microtubule. Particles were also observed to switch from one microtubule to another as they were transported. The polarity of the microtubules did not seem to affect the particle direction, since particles were observed to move in both directions on the same MTLE. When not in motion these particles behaved as if anchored to the microtubules since they showed negligible Brownian motion. Finally, it was observed that an elongate particle could move onto two intersecting linear elements such that it was deformed into an inverted "Y" shape. This indicates that there may be more than a single site of attachment between the force generator and the particle.
我们首次直接证明了细胞器和囊泡(统称为颗粒)的细胞质运输是沿着微管进行的。使用艾伦视频增强对比度、微分干涉对比度(AVEC-DIC)显微镜[艾伦等人,1981年]观察了来自牛蛙角膜基质的活角膜细胞。在这些细胞足够薄的区域中,可以看到一个线性元件网络。当观察到颗粒运动时,它们总是沿着这些线性元件移动。当在稳定微管的细胞裂解液中裂解时,线性元件在显微镜下保持完整并聚焦。然后将制剂用甲醛固定,用磷酸盐缓冲盐水(PBS)洗涤,用兔抗微管蛋白孵育,用PBS洗涤,用罗丹明偶联的山羊抗兔染色,并用PBS洗涤。在整个这些过程中,提取的细胞继续保持在原位并在显微镜下聚焦。然后使用落射荧光光学器件和硅增强靶(SIT)摄像机观察相同的细胞。可以看到一个荧光线性元件网络在数量、形态和位置上与在实时AVEC-DIC图像中看到的线性元件相对应。综合起来,AVEC-DIC和荧光显微镜观察证明颗粒沿着其移动的线性元件是微管(MTLEs)。即使对于同一微管上的同一颗粒,观察到的颗粒速度、暂停时间和移动距离也有很大差异。还观察到颗粒在运输过程中从一根微管切换到另一根微管。微管的极性似乎不影响颗粒方向,因为在同一MTLE上观察到颗粒向两个方向移动。当不运动时,这些颗粒表现得好像锚定在微管上,因为它们显示出可忽略不计的布朗运动。最后,观察到一个细长颗粒可以移动到两个相交的线性元件上,使其变形为倒“Y”形。这表明力发生器和颗粒之间可能存在不止一个附着位点。