Müller H W, Ignatius M J, Hangen D H, Shooter E M
J Cell Biol. 1986 Feb;102(2):393-402. doi: 10.1083/jcb.102.2.393.
Protein synthesis in the nerve sheath of injured as well as intact mature and developing sciatic nerves from rat and rabbit was investigated by incubating segments of nerve with [35S]methionine in vitro. The composition of labeled proteins under the different conditions of nerve growth was analyzed by two-dimensional gel electrophoresis and fluorography. The expression of six secreted proteins in rat sciatic nerve with the apparent molecular weights of 70,000 (70 kD), 54,000 (54 kD), 51,000 (51 kD), 39,000 (39 kD), 37,000 (37 kD), and 30,000 (30 kD) was of particular interest because of the correlation of their synthesis and secretion with aspects of nerve growth and regeneration. The synthesis of the 37-kD protein was significantly stimulated during both sciatic nerve development as well as regeneration but not in the intact mature nerve. The expression of this protein appears to be regulated by signal(s) from the axon but not the target. The 70-kD protein was exclusively synthesized in response to axotomy, thus confining its role to some aspect(s) of nerve repair. In contrast, the 54- and 51-kD proteins were expressed in the intact mature nerve sheath. Their synthesis and release was rapidly inhibited upon axotomy but returned to normal or higher levels towards the end of sciatic nerve regeneration, suggesting a role in the maintenance of the integrity of the mature (nongrowing) rat nerve. The 39- and 30-kD proteins were only transiently synthesized within the first week after axotomy. Two proteins with the apparent molecular masses of 70 and 37 kD were synthesized in denervated rabbit sciatic nerve. The similar molecular weights, net charges, and time-courses of induction suggest a homology between these proteins in rabbit and rat, indicating common molecular responses of peripheral nerve sheath cells to axon injury in both mammalian species.
通过在体外将大鼠和兔的坐骨神经节段与[35S]甲硫氨酸一起孵育,研究了损伤的以及完整的成熟和发育中的大鼠和兔坐骨神经神经鞘中的蛋白质合成。通过二维凝胶电泳和荧光自显影分析了在不同神经生长条件下标记蛋白质的组成。大鼠坐骨神经中六种分泌蛋白的表达尤为令人感兴趣,其表观分子量分别为70,000(70 kD)、54,000(54 kD)、51,000(51 kD)、39,000(39 kD)、37,000(37 kD)和30,000(30 kD),因为它们的合成和分泌与神经生长和再生的各个方面相关。在坐骨神经发育以及再生过程中,37-kD蛋白的合成受到显著刺激,但在完整的成熟神经中则不然。该蛋白的表达似乎受轴突发出的信号调节,而非靶标的信号调节。70-kD蛋白仅在轴突切断后合成,因此其作用局限于神经修复的某些方面。相反,54-kD和51-kD蛋白在完整的成熟神经鞘中表达。轴突切断后,它们的合成和释放迅速受到抑制,但在坐骨神经再生末期恢复到正常或更高水平,这表明它们在维持成熟(非生长)大鼠神经的完整性方面发挥作用。39-kD和30-kD蛋白仅在轴突切断后的第一周内短暂合成。在去神经支配的兔坐骨神经中合成了两种表观分子量分别为70和37 kD的蛋白。相似的分子量、净电荷和诱导时间进程表明这些蛋白在兔和大鼠中具有同源性,这表明两种哺乳动物的外周神经鞘细胞对轴突损伤具有共同的分子反应。