Schlaepfer W W, Micko S
J Cell Biol. 1978 Aug;78(2):369-78. doi: 10.1083/jcb.78.2.369.
The sequence of changes occurring in transected rat sciatic nerve was examined by electron microscopy and by sodium dodecyl sulfate (SDS) polyacrylamide disc gel electrophoresis. Representative segments of transected nerves were processed for ultrastructural examinations between 0 and 34 days after the transection of sciatic nerves immediately below the sacro-sciatic notch. The remainder of the transected nerves and the intact portions of sciatic nerves were desheathed and immediately homogenized in 1 percent SDS containing 8 M urea and 50 mM dithioerythritol. Solubilized proteins were analyzed on 12 percent gels at pH 8.3 in a discontinuous electrophoretic system. Initial changes were limited to the axons of transected nerve fibers and were characterized by the loss of microtubules and neurofilaments and their replacement by an amorphous floccular material. These changes became widespread between 24 and 48 h after transection. The disruption of neurofilaments during this interval occurred in parallel with a selective loss of 69,000, 150,000 and 200,000 mol wt proteins from nerve homogenates, thus corroborating the view that these proteins represent component subunits of mammalian neurofilaments. Furthermore, the selective changes of neurofilament proteins in transected nerves indicate their inherent lability and suggest their susceptibility to calcium-mediated alterations. Electrophoretic profiles of nerve proteins during the 4-34-day interval after nerve transection reflected the breakdown and removal of myelin, the proliferation of Schwann cells and the deposition of endoneurial collagen. A marked increase of intermediate-sized filaments within proliferating Schwann cell processes was not accompanied by the appearance of neurofilamentlike proteins in gels of nerve homogenates.
通过电子显微镜以及十二烷基硫酸钠(SDS)聚丙烯酰胺圆盘凝胶电泳,对切断的大鼠坐骨神经中发生的一系列变化进行了研究。在坐骨神经于骶-坐骨切迹下方立即切断后的0至34天之间,对切断神经的代表性节段进行超微结构检查。将切断神经的其余部分以及坐骨神经的完整部分剥除神经鞘,并立即在含有8M尿素和50mM二硫苏糖醇的1%SDS中匀浆。在不连续电泳系统中,于pH 8.3的12%凝胶上分析溶解的蛋白质。最初的变化仅限于切断神经纤维的轴突,其特征是微管和神经丝的丧失,并被无定形絮状物质所取代。这些变化在切断后24至48小时内变得普遍。在此期间神经丝的破坏与神经匀浆中69,000、150,000和200,000分子量蛋白质的选择性丧失同时发生,从而证实了这些蛋白质代表哺乳动物神经丝组成亚基的观点。此外,切断神经中神经丝蛋白的选择性变化表明其固有的不稳定性,并提示它们易受钙介导的改变影响。神经切断后4至34天期间神经蛋白的电泳图谱反映了髓磷脂的分解和清除、雪旺细胞的增殖以及神经内膜胶原的沉积。增殖的雪旺细胞突起内中等大小细丝的显著增加,并未伴随着神经匀浆凝胶中出现神经丝样蛋白。