Uchida Atsuko, Monsma Paula C, Fenn J Daniel, Brown Anthony
Department of Neuroscience, The Ohio State University, Columbus, OH, USA.
Methods Cell Biol. 2016;131:21-90. doi: 10.1016/bs.mcb.2015.07.001. Epub 2015 Sep 2.
Neurofilaments, which are the intermediate filaments of nerve cells, are space-filling cytoskeletal polymers that contribute to the growth of axonal caliber. In addition to their structural role, neurofilaments are cargos of axonal transport that move along microtubule tracks in a rapid, intermittent, and bidirectional manner. Though they measure just 10nm in diameter, which is well below the diffraction limit of optical microscopes, these polymers can reach 100 μm or more in length and are often packed densely, just tens of nanometers apart. These properties of neurofilaments present unique challenges for studies on their movement. In this article, we describe several live-cell fluorescence imaging strategies that we have developed to image neurofilament transport in axons of cultured neurons on short and long timescales. Together, these methods form a powerful set of complementary tools with which to study the axonal transport of these unique intracellular cargos.
神经丝是神经细胞的中间丝,是填充空间的细胞骨架聚合物,有助于轴突管径的生长。除了其结构作用外,神经丝还是轴突运输的货物,以快速、间歇和双向的方式沿着微管轨道移动。尽管它们的直径仅为10纳米,远低于光学显微镜的衍射极限,但这些聚合物的长度可达100微米或更长,并且通常密集排列,彼此之间仅相隔几十纳米。神经丝的这些特性为研究其运动带来了独特的挑战。在本文中,我们描述了几种活细胞荧光成像策略,这些策略是我们为在短期和长期时间尺度上对培养神经元轴突中的神经丝运输进行成像而开发的。这些方法共同构成了一套强大的互补工具,可用于研究这些独特的细胞内货物的轴突运输。