Shyne-Athwal S, Chakraborty G, Gage E, Ingoglia N A
Department of Physiology, UMDNJ-New Jersey Medical School, Newark 07103-2757.
Exp Neurol. 1988 Feb;99(2):281-95. doi: 10.1016/0014-4886(88)90148-3.
Posttranslational protein modifications by the addition of amino acids are reactions which occur in intact sciatic and optic nerves of rats. The nerves differ, however, in that 2 h after crush injury these reactions are activated in sciatic but not in optic nerves. As sciatic nerves will eventually regenerate, whereas optic nerves will not, we have proposed that the activation of these reactions is correlated with the ability of a nerve to regenerate. The current experiments examined the posttranslational addition of amino acids to proteins at times greater than 2 h after nerve crush, during sciatic nerve regeneration and optic nerve degeneration. We also examined the optic nerve for morphologic correlates to changes in protein modification and partially characterized the proteins modified by [3H]Lys in the regenerating sciatic nerve using two-dimensional sodium dodecyl sulfate (SDS)-polyacrylamide gel electrophoresis (PAGE). In a segment of sciatic nerve taken from a region just proximal to the site of crush, protein modification by covalent addition of [3H]Arg, [3H]Lys and [3H]Leu increased during both posttraumatic (2 h postcrush) and regenerative (6 days and 14 days postcrush) stages. Two-dimensional PAGE of [3H]Lys modified sciatic nerve proteins 6 days after crush injury showed labeling of proteins having molecular masses in the 18,000- to 20,000-, 30,000- to 40,000-, and 80,000- to 100,000-Da ranges, with neutral or basic isoelectric points (pI 7.1 to 8.0). In the retinal portion of the crushed optic nerve, incorporation of the same amino acids was unchanged or depressed to 21 days postcrush, except at 6 days postcrush when the incorporation of all three amino acids into proteins was increased threefold. These increases correlated with the appearance of terminal end bulbs in the portion of nerve analyzed. Histological examination of each nerve 2 h postcrush showed marked edema in the optic but not the sciatic nerve, a condition which may be related to the ability of sciatic and inability of optic nerves to activate protein modification reactions.
通过添加氨基酸进行的蛋白质翻译后修饰反应发生在大鼠完整的坐骨神经和视神经中。然而,这两种神经存在差异,在挤压伤后2小时,这些反应在坐骨神经中被激活,而在视神经中未被激活。由于坐骨神经最终会再生,而视神经不会,我们提出这些反应的激活与神经的再生能力相关。当前的实验研究了在神经挤压后超过2小时、坐骨神经再生和视神经退变期间蛋白质翻译后添加氨基酸的情况。我们还检查了视神经中与蛋白质修饰变化相关的形态学特征,并使用二维十二烷基硫酸钠(SDS)-聚丙烯酰胺凝胶电泳(PAGE)部分鉴定了再生坐骨神经中被[3H]赖氨酸修饰的蛋白质。在取自挤压部位近端区域的一段坐骨神经中,在创伤后(挤压后2小时)和再生阶段(挤压后6天和14天),通过共价添加[3H]精氨酸、[3H]赖氨酸和[3H]亮氨酸进行的蛋白质修饰均增加。挤压伤后6天,对[3H]赖氨酸修饰的坐骨神经蛋白质进行二维PAGE分析,结果显示分子量在18,000至20,000、三万至四万和八万至十万道尔顿范围内的蛋白质被标记,其等电点为中性或碱性(pI 7.1至8.0)。在挤压视神经的视网膜部分,相同氨基酸的掺入在挤压后21天之前保持不变或降低,不过在挤压后6天时,所有三种氨基酸掺入蛋白质的量增加了两倍。这些增加与所分析神经部分中终末球的出现相关。挤压伤后2小时对每条神经进行组织学检查发现,视神经中有明显水肿,而坐骨神经中没有,这种情况可能与坐骨神经激活蛋白质修饰反应的能力以及视神经无法激活该反应的能力有关。