Chang S, Svitkina T M, Borisy G G, Popov S V
Department of Physiology and Biophysics M/C 901, University of Illinois at Chicago, 835 South Wolcott Avenue, Chicago, Illinois 60612, USA.
Nat Cell Biol. 1999 Nov;1(7):399-403. doi: 10.1038/15629.
Assembly of microtubules is fundamental to neuronal morphogenesis. Microtubules typically form crosslinked bundles in nerve processes, precluding resolution of single microtubules at the light microscopic level. Therefore, previous studies of microtubule transport in neurites have had to rely on indirect approaches. Here we show that individual microtubules can be visualized directly in the axonal shafts of Xenopus embryo neurons by using digital fluorescence microscopy. We find that, although the array of axonal microtubules is dynamic, microtubules are stationary relative to the substrate. These results argue against a model in which newly synthesized tubulin is transported down the axon in the form of microtubules.
微管组装对于神经元形态发生至关重要。微管通常在神经突起中形成交联束,这使得在光学显微镜水平上无法分辨单个微管。因此,先前对神经突中微管运输的研究不得不依赖间接方法。在这里,我们表明通过使用数字荧光显微镜可以直接在非洲爪蟾胚胎神经元的轴突中观察到单个微管。我们发现,尽管轴突微管阵列是动态的,但微管相对于底物是静止的。这些结果与一种模型相悖,该模型认为新合成的微管蛋白以微管的形式沿轴突运输。