Perry G W, Burmeister D W, Grafstein B
J Neurochem. 1985 Apr;44(4):1142-51. doi: 10.1111/j.1471-4159.1985.tb08736.x.
After the goldfish optic nerve was crushed, the total amount of protein in the nerve decreased by about 45% within 1 week as the axons degenerated, began to recover between 2 and 5 weeks as axonal regeneration occurred, and had returned to nearly normal by 12 weeks. Corresponding changes in the relative amounts of some individual proteins were investigated by separating the proteins by two-dimensional gel electrophoresis and performing a quantitative analysis of the Coomassie Brilliant Blue staining patterns of the gels. In addition, labelling patterns showing incorporation of [3H]proline into individual proteins were examined to differentiate between locally synthesized proteins (presumably produced mainly by the glial cells) and axonal proteins carried by fast or slow axonal transport. Some prominent nerve proteins, ON1 and ON2 (50-55 kD, pI approximately 6), decreased to almost undetectable levels and then reappeared with a time course corresponding to the changes in total protein content of the nerve. Similar changes were seen in a protein we have designated NF (approximately 130 kD, pI approximately 5.2). These three proteins, which were labelled in association with slow axonal transport, may be neurofilament constituents. Large decreases following optic nerve crush were also seen in the relative amounts of alpha- and beta-tubulin, which suggests that they are localized mainly in the optic axons rather than the glial cells. Another group of proteins, W2, W3, and W4 (35-45 kD, pI 6.5-7.0), which showed a somewhat slower time course of disappearance and were intensely labelled in the local synthesis pattern, may be associated with myelin. A small number of proteins increased in relative amount following nerve crush. These included some, P1 and P2 (35-40 kD, pIs 6.1-6.2) and NT (approximately 50 kD, pI approximately 5.5), that appeared to be synthesized by the glial cells. Increases were also seen in one axonal protein, B (approximately 45 kD, pI approximately 4.5), that is carried by fast axonal transport, as well as in two axonal proteins, HA1 and HA2 (approximately 60 and 65 kD respectively, pIs 4.5-5.0), that are carried mainly by slow axonal transport. Other proteins, including actin, that showed no net changes in relative amount (but presumably changed in absolute amount in direct proportion to the changes in total protein content of the nerve), are apparently distributed in both the neuronal and nonneuronal compartments of the nerve.
金鱼视神经被挤压后,随着轴突退化,神经中的蛋白质总量在1周内下降了约45%;在2至5周之间,随着轴突再生开始恢复;到12周时已恢复到接近正常水平。通过二维凝胶电泳分离蛋白质并对凝胶的考马斯亮蓝染色模式进行定量分析,研究了一些个别蛋白质相对含量的相应变化。此外,还检查了显示[3H]脯氨酸掺入个别蛋白质的标记模式,以区分局部合成的蛋白质(可能主要由神经胶质细胞产生)和通过快速或慢速轴突运输携带的轴突蛋白质。一些突出的神经蛋白,ON1和ON2(50 - 55kD,pI约为6),下降到几乎检测不到的水平,然后随着与神经总蛋白含量变化相对应的时间进程重新出现。在我们命名为NF(约130kD,pI约为5.2)的一种蛋白质中也观察到了类似的变化。这三种与慢速轴突运输相关标记的蛋白质可能是神经丝成分。视神经挤压后,α-微管蛋白和β-微管蛋白的相对含量也大幅下降,这表明它们主要定位于视神经轴突而非神经胶质细胞中。另一组蛋白质,W2、W3和W4(35 - 45kD,pI 6.5 - 7.0),其消失的时间进程稍慢,并且在局部合成模式中被强烈标记,可能与髓磷脂有关。少数蛋白质在神经挤压后相对含量增加。这些包括一些似乎由神经胶质细胞合成的蛋白质,P1和P2(35 - 40kD,pI 6.1 - 6.2)以及NT(约50kD,pI约为5.5)。在一种通过快速轴突运输携带的轴突蛋白B(约45kD,pI约为4.5)以及两种主要通过慢速轴突运输携带的轴突蛋白HA1和HA2(分别约为60kD和65kD,pI 4.5 - 5.0)中也观察到了增加。其他蛋白质,包括肌动蛋白,其相对含量没有净变化(但绝对量可能与神经总蛋白含量的变化成正比),显然分布在神经的神经元和非神经元部分。