Glass J D, Schryer B L, Griffin J W
Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21287-6965.
J Neurochem. 1994 Jun;62(6):2472-5. doi: 10.1046/j.1471-4159.1994.62062472.x.
The C57BL/Ola (Ola) mouse is a mutant substrain in which transected axons undergo very slow Wallerian degeneration. Because axonal degradation during Wallerian degeneration is calcium dependent, we tested whether Ola axons are susceptible to calcium-mediated axonal degeneration by comparing neurofilament degradation between Ola and C57BL/6 mice in sciatic nerve explants. Using immunoblot analysis of neurofilament degradation and electron microscopy we found that as in normal axons, axonal degeneration in the Ola is calcium dependent. However, when compared with normal animals, higher levels of calcium were required for complete degradation of neurofilaments in Ola nerve, suggesting a relative insensitivity to calcium-mediated degeneration in the Ola. We conclude that calcium-activated proteases are present and active in Ola axons but that higher levels of calcium are required to accomplish complete axonal degradation. These results suggest a possible mechanism for prolonged survival of transected Ola axons and provide potential insight into the pathophysiology of axonal degeneration in injury and disease.
C57BL/Ola(Ola)小鼠是一种突变亚系,其中横断的轴突会经历非常缓慢的华勒氏变性。由于华勒氏变性过程中的轴突降解是钙依赖性的,我们通过比较坐骨神经外植体中Ola小鼠和C57BL/6小鼠的神经丝降解情况,来测试Ola轴突是否易受钙介导的轴突变性影响。通过对神经丝降解的免疫印迹分析和电子显微镜观察,我们发现,与正常轴突一样,Ola小鼠的轴突变性也是钙依赖性的。然而,与正常动物相比,Ola神经中神经丝完全降解需要更高水平的钙,这表明Ola小鼠对钙介导的变性相对不敏感。我们得出结论,钙激活蛋白酶在Ola轴突中存在且有活性,但需要更高水平的钙才能完成轴突的完全降解。这些结果提示了横断的Ola轴突延长存活的一种可能机制,并为损伤和疾病中轴突变性的病理生理学提供了潜在的见解。