Schiffer Davide, Fiano Valentina
Department of Neuroscience, University of Turin, Via Cherasco 15, 10126 Turin, Italy.
Amyotroph Lateral Scler Other Motor Neuron Disord. 2004 Mar;5(1):22-5. doi: 10.1080/14660820310016822.
Literature findings on astrogliosis of the spinal cord and of the cortex of sporadic (SALS) and familial (FALS) cases of amyotrophic lateral sclerosis (ALS) and of SOD1 transgenic mice are analysed and compared with those of 50 autopsied personal cases of ALS. In the spinal cord, astrogliosis is definitely evident in the anterior horns and much less in anterior and lateral funiculi and dorsal horns. In the cortex reactive astrocytes show a distribution similar to that of ageing brains and in ischaemia and cannot be directly put in relation with neuronal loss. In the spinal cord of transgenic mice the evidence suggests a primary astrocytic response. The findings in human ALS, especially those of the cortex, are consistent with this hypothesis.
对散发性(SALS)和家族性(FALS)肌萎缩侧索硬化症(ALS)病例以及超氧化物歧化酶1(SOD1)转基因小鼠的脊髓和皮质星形胶质细胞增生的文献研究结果进行了分析,并与50例ALS尸检病例的结果进行了比较。在脊髓中,前角的星形胶质细胞增生明显,而在前索、外侧索和后角则较少。在皮质中,反应性星形胶质细胞的分布与衰老大脑和缺血时相似,与神经元丢失无直接关联。在转基因小鼠的脊髓中,证据表明存在原发性星形胶质细胞反应。人类ALS的研究结果,尤其是皮质的研究结果,与这一假设相符。