Division of Neurobiology and Anatomy, Graduate School of Medical and Dental Sciences, Niigata University, Niigata 951-8510, Japan; Department of Biochemistry and Molecular Biology, Jahangirnagar University, Savar, Dhaka 1342, Bangladesh.
Division of Neurobiology and Anatomy, Graduate School of Medical and Dental Sciences, Niigata University, Niigata 951-8510, Japan.
Neurochem Int. 2018 Oct;119:159-170. doi: 10.1016/j.neuint.2017.10.009. Epub 2017 Oct 21.
Dystonia musculorum (dt) mice, which have a mutation in the Dystonin (Dst) gene, are used as animal models to investigate the human disease known as hereditary sensory and autonomic neuropathy type VI. Massive neuronal cell death is observed, mainly in the peripheral nervous system (PNS) of dt mice. We and others have recently reported a histopathological feature of these mice that neurofilament (NF) accumulates in various areas of the central nervous system (CNS), including motor pathways. Although dt mice show motor disorder and growth retardation, the causes for these are still unknown. Here we performed histopathological analyses on motor units of the trigeminal motor nucleus (Mo5 nucleus), because they are a good system to understand neuronal responses in the mutant CNS, and abnormalities in this system may lead to problems in mastication, with subsequent growth retardation. We report that motoneurons with NF accumulation in the Mo5 nuclei of Dst homozygous mice express the stress-induced genes CHOP, ATF3, and lipocalin 2 (Lcn2). We also show a reduced number of Mo5 motoneurons and a reduced size of Mo5 nuclei in Dst homozygous mice, possibly due to apoptosis, given the presence of cleaved caspase 3-positive Mo5 motoneurons. In the mandibular (V3) branches of the trigeminal nerve, which contains axons of Mo5 motoneurons and trigeminal sensory neurons, there was infiltration of Iba1-positive macrophages. Finally, we report atrophy of the masseter muscles in Dst homozygous mice, which showed abnormal nuclear localization of myofibrils and increased expression of atrogin-1 mRNA, a muscle atrophy-related gene and weaker masseter muscle strength with uncontrolled muscle activity by electromyography (EMG). Taken together, our findings strongly suggest that mastication in dt mice is affected due to abnormalities of Mo5 motoneurons and masseter muscles, leading to growth retardation at the post-weaning stages.
肌肉型张力障碍(dt)小鼠的 Dystonin(Dst)基因突变,被用作研究人类遗传性感觉自主神经病 VI 型疾病的动物模型。大量神经元细胞死亡,主要发生在 dt 小鼠的外周神经系统(PNS)。我们和其他人最近报道了这些小鼠的一种组织病理学特征,即神经丝(NF)在中枢神经系统(CNS)的各个区域积聚,包括运动通路。尽管 dt 小鼠表现出运动障碍和生长迟缓,但这些原因仍不清楚。在这里,我们对三叉神经运动核(Mo5 核)的运动单位进行了组织病理学分析,因为它们是了解突变 CNS 中神经元反应的良好系统,并且该系统的异常可能导致咀嚼问题,随后导致生长迟缓。我们报告说,在 Dst 纯合子小鼠的 Mo5 核中积聚 NF 的运动神经元表达应激诱导基因 CHOP、ATF3 和脂联素 2(Lcn2)。我们还显示 Dst 纯合子小鼠的 Mo5 运动神经元数量减少,Mo5 核体积减小,可能是由于存在 cleaved caspase 3 阳性的 Mo5 运动神经元而导致凋亡。在三叉神经的下颌(V3)分支中,含有 Mo5 运动神经元和三叉神经感觉神经元的轴突,有 Iba1 阳性巨噬细胞浸润。最后,我们报告说 Dst 纯合子小鼠的咬肌萎缩,其肌纤维核定位异常,肌肉萎缩相关基因atrogin-1 mRNA 表达增加,并且肌电图(EMG)显示肌肉活动不受控制时咬肌力量减弱。综上所述,我们的研究结果强烈表明,由于 Mo5 运动神经元和咬肌异常,dt 小鼠的咀嚼功能受到影响,导致断奶后阶段生长迟缓。