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尼曼-匹克病C型小鼠模型中的脑干神经病理学

Brainstem neuropathology in a mouse model of Niemann-Pick disease type C.

作者信息

Luan Zhuo, Saito Yoshiaki, Miyata Hajime, Ohama Eisaku, Ninomiya Haruaki, Ohno Kousaku

机构信息

Division of Child Neurology, Institute of Neurological Sciences, Faculty of Medicine, Tottori University, Japan.

出版信息

J Neurol Sci. 2008 May 15;268(1-2):108-16. doi: 10.1016/j.jns.2007.11.018. Epub 2008 Jan 10.

Abstract

Niemann-Pick disease type C (NPC) is a neurovisceral lipid storage disorder characterized by progressive and widespread neurodegeneration. Although some characteristic symptoms of NPC result from brainstem dysfunction, little information is available about which brainstem structures are affected. In this study, the brainstems of mutant BALB/c NPC1-/- mice with a retroposon insertion in the NPC1 gene were examined for neuropathological changes. In the midbrain, the integrated optic density (IOD) and cell count density of tyrosine-hydroxylase (TH) immunostained neurons were decreased in the substantia nigra. In the pons, TH immunoreactivity in the locus ceruleus (LC) neurons was decreased, while the IOD and the neuronal density of choline acetyltransferase (ChAT)-immunostained neurons in the pedunculopontine tegmental nucleus were preserved. The ChAT immunoreactivity of the hypoglossal nucleus (12N) neurons was not decreased, but Klüver-Barrera staining showed that neuronal density in the nucleus of the solitary tract (NTS) was decreased. Klüver-Barrera and neuronal nuclei (NeuN) staining showed a decrease in neuronal density in the ventral cochlear nucleus, but not in the dorsal cochlear nucleus. Gliosis was widely identified by GFAP staining in various brainstem structures, including the superior and inferior colliculi, the rostral interstitial nucleus of the medial longitudinal fasciculus, the oculomotor complex, the medial geniculate nucleus, the nucleus ambiguus, and the 12N. However, GFAP expression was not augmented in the LC, the cochlear nucleus, or the NTS. These neuropathological findings suggest a basis for the neurological syndromes observed in NPC, such as rigidity, oculomotor symptoms, cataplexy and sleep disturbance, dysphagia, and perceptive deafness.

摘要

尼曼-匹克病C型(NPC)是一种神经内脏脂质贮积病,其特征为进行性和广泛性神经退行性变。尽管NPC的一些特征性症状源于脑干功能障碍,但关于哪些脑干结构受到影响的信息却很少。在本研究中,对NPC1基因中存在逆转座子插入的突变BALB/c NPC1-/-小鼠的脑干进行了神经病理学变化检查。在中脑,黑质中酪氨酸羟化酶(TH)免疫染色神经元的积分光密度(IOD)和细胞计数密度降低。在脑桥,蓝斑(LC)神经元中的TH免疫反应性降低,而脚桥被盖核中胆碱乙酰转移酶(ChAT)免疫染色神经元的IOD和神经元密度保持不变。舌下神经核(12N)神经元的ChAT免疫反应性未降低,但克吕弗-巴雷拉染色显示孤束核(NTS)中的神经元密度降低。克吕弗-巴雷拉染色和神经元细胞核(NeuN)染色显示腹侧耳蜗核中的神经元密度降低,但背侧耳蜗核中未降低。通过胶质纤维酸性蛋白(GFAP)染色在包括上丘和下丘、内侧纵束的嘴侧间质核、动眼神经复合体、内侧膝状体核、疑核和12N在内的各种脑干结构中广泛发现了胶质增生。然而,LC、耳蜗核或NTS中的GFAP表达没有增加。这些神经病理学发现为NPC中观察到的神经综合征,如僵硬、动眼神经症状、猝倒和睡眠障碍、吞咽困难以及感音神经性耳聋,提供了一个基础。

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