King C E, Canty A J, Vickers J C
Neurodegeneration Research Laboratory, Discipline of Pathology, Faculty of Health Sciences, University of Tasmania, 43 Collins Street, Hobart, Tasmania 7000, Australia.
Neuropathol Appl Neurobiol. 2001 Apr;27(2):115-26. doi: 10.1046/j.1365-2990.2001.00317.x.
In order to study the changes in axons related to acute localized physical trauma, a 25 gauge needle was inserted into the somatosensory cortex of anaesthetized adult rats. Animals were examined over 11 time points, from 30 min to 14 days postinjury. Initially, the central needle tract was surrounded by 'reactive' abnormal axons characterized by their bulb- or ring-like immunoreactivity for neurofila ments. Quantification demonstrated that these structures reached a peak density at 24 h postinjury, followed by a gradual decrease over 2 weeks. By 5 days postinjury, long axons showing high levels of neurofilament labelling were localized to the lesion area, either aligned parallel to the tract edges or extending into the bridge of tissue forming between the tract edges. Double-labelling demonstrated a close association between sprouting axons and ferritin-labelled microglia. Immunolabelling for GAP43 also demonstrated the presence of sprouting axons within this tissue bridge. Ultrastuctural examination showed that sprouting axons contained a high density of neurofilaments, with a leading edge lacking these filaments. Injury to the adult neocortex is associated with reactive and sprouting changes within axons, coordinated with the proliferation of microglia and wound healing. These data also support a role for neurofilaments in axonal sprouting following brain injury.
为了研究与急性局部物理创伤相关的轴突变化,将一根25号针插入麻醉成年大鼠的体感皮层。在损伤后30分钟至14天的11个时间点对动物进行检查。最初,中央针道被“反应性”异常轴突包围,这些轴突对神经丝具有球状或环状免疫反应性。定量分析表明,这些结构在损伤后24小时达到峰值密度,随后在2周内逐渐下降。损伤后5天,显示高水平神经丝标记的长轴突定位于病变区域,要么与针道边缘平行排列,要么延伸到针道边缘之间形成的组织桥中。双重标记显示出芽轴突与铁蛋白标记的小胶质细胞之间密切相关。对GAP43的免疫标记也证明了该组织桥内存在出芽轴突。超微结构检查显示,出芽轴突含有高密度的神经丝,其前缘缺乏这些细丝。成年新皮层损伤与轴突内的反应性和出芽变化相关,与小胶质细胞的增殖和伤口愈合相协调。这些数据也支持神经丝在脑损伤后轴突出芽中的作用。