Brown A, Slaughter T, Black M M
Department of Anatomy and Cell Biology, Temple University School of Medicine, Philadelphia, Pennsylvania 19140.
J Cell Biol. 1992 Nov;119(4):867-82. doi: 10.1083/jcb.119.4.867.
We have investigated the sites of microtubule (MT) assembly in neurons during axon growth by taking advantage of the relationship between the proportion of tyrosinated alpha-tubulin (tyr-tubulin) in MTs and their age. Specifically, young (newly assembled) MTs contain more tyr-tubulin than older (more long-lived) MTs. To quantify the relative proportion of tyr-tubulin in MTs, cultured rat sympathetic neurons were permeabilized under conditions that stabilize existing MTs and remove unassembled tubulin. The MTs were then double-stained with antibodies to tyr-tubulin (as a measure of the amount of tyr-tubulin in MTs) and to beta-tubulin (as a measure of total MT mass), using immunofluorescence procedures. Cells were imaged with a cooled charge-coupled device camera and the relative proportion of tyr-tubulin in the MTs was quantified by computing the ratio of the tyr-tubulin fluorescence to the beta-tubulin fluorescence using a novel application of digital image processing and analysis techniques. The amount of tyr-tubulin in the MTs was highest in the cell body and at the growth cone; peak ratios in these two regions were approximately 10-fold higher than for the axon shaft. Moving out from the cell body into the axon, the tyr-tubulin content declined over an average distance of 40 microns to reach a constant low value within the axon shaft and then rose again more distally, over an average distance of 110 microns, to reach a peak at the growth cone (average axon length = 358 microns). These observations indicate that newly assembled MTs are concentrated in the proximal and distal regions of growing axons and therefore that the cell body and growth cone are the most active sites of MT assembly dynamics in neurons that are actively extending axons.
我们利用微管(MT)中酪氨酸化α-微管蛋白(tyr-微管蛋白)的比例与其年龄之间的关系,研究了轴突生长过程中神经元内微管组装的位点。具体而言,年轻的(新组装的)微管比年长的(寿命更长的)微管含有更多的tyr-微管蛋白。为了量化微管中tyr-微管蛋白的相对比例,在稳定现有微管并去除未组装微管蛋白的条件下,使培养的大鼠交感神经元通透化。然后,使用免疫荧光程序,用抗tyr-微管蛋白的抗体(作为微管中tyr-微管蛋白量的指标)和抗β-微管蛋白的抗体(作为总微管质量的指标)对微管进行双重染色。用冷却的电荷耦合器件相机对细胞成像,并通过使用数字图像处理和分析技术的新应用,计算tyr-微管蛋白荧光与β-微管蛋白荧光的比率,来量化微管中tyr-微管蛋白的相对比例。微管中tyr-微管蛋白的量在细胞体和生长锥中最高;这两个区域的峰值比率比轴突干大约高10倍。从细胞体向轴突移动时,tyr-微管蛋白含量在平均40微米的距离内下降,在轴突干内达到恒定的低值,然后在更远端又上升,平均距离为110微米,在生长锥处达到峰值(平均轴突长度 = 358微米)。这些观察结果表明,新组装的微管集中在生长轴突的近端和远端区域,因此细胞体和生长锥是正在积极延伸轴突的神经元中微管组装动态最活跃的位点。