Department of Neurology, The Second Hospital of Hebei Medical University, Hebei 050000, China.
Brain Res. 2012 Jun 15;1460:88-95. doi: 10.1016/j.brainres.2012.04.003. Epub 2012 Apr 12.
TAR DNA-binding protein 43 (TDP-43) has been found to be related to the pathogenesis of amyotrophic lateral sclerosis (ALS). TDP-43 A315T transgenic mice develop degeneration of specific motor neurons, and accumulation of ubiquitinated proteins has been observed in the pyramidal cells of motor cortex of these mice. In this study, we found stress-responsive HO-1 induction and no autophagic alteration in motor cortex of TDP-43 A315T transgenic mice. Glial activation, especially astrocytic proliferation, occurred in cortical layer 5 and sub-meningeal region. Interestingly, we noticed that progressively thinned colon, swollen small intestine and reduced food intake, rather than severe muscle weakness, contributed to the death of TDP-43 A315T transgenic mice. Increased TDP-43 accumulation in the myenteric nerve plexus and increased thickness of muscular layer of colon were related to the intestinal dysfunction.
TAR DNA 结合蛋白 43(TDP-43)与肌萎缩性侧索硬化症(ALS)的发病机制有关。TDP-43 A315T 转基因小鼠出现特定运动神经元的退化,并且在这些小鼠的运动皮层的锥体神经元中观察到泛素化蛋白的积累。在这项研究中,我们发现 TDP-43 A315T 转基因小鼠的运动皮层中应激反应性 HO-1 诱导和自噬改变。胶质细胞激活,特别是星形胶质细胞增殖,发生在皮质 5 层和脑膜下区域。有趣的是,我们注意到逐渐变薄的结肠、肿胀的小肠和减少的食物摄入,而不是严重的肌肉无力,导致 TDP-43 A315T 转基因小鼠的死亡。在肌间神经丛中 TDP-43 的积累增加和结肠肌肉层厚度的增加与肠道功能障碍有关。