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一种新型的动力蛋白重链突变 Loa 表型:树突形态改变、细胞器密度降低以及三叉运动神经元数量减少。

A novel phenotype for the dynein heavy chain mutation Loa: altered dendritic morphology, organelle density, and reduced numbers of trigeminal motoneurons.

机构信息

Department of Physiology & Cell Biology, University of Nevada School of Medicine, Reno, Nevada 89557, USA.

出版信息

J Comp Neurol. 2012 Aug 15;520(12):2757-73. doi: 10.1002/cne.23085.

Abstract

Dynein, the retrograde motor protein, is essential for the transport of cargo along axons and proximal dendrites in neurons. The dynein heavy chain mutation Loa has been reported to cause degeneration of spinal motor neurons, as well as defects of spinal sensory proprioceptive neurons, but cranial nerve nuclei have received little attention. Here, we examined the number and morphology of neurons in cranial nerve nuclei of young, adult, and aged heterozygous Loa mice, with a focus on the trigeminal, facial, and trochlear motor nuclei, as well as the proprioceptive mesencephalic trigeminal nucleus. By using stereological counting techniques, we report a slowly progressive and significant reduction, to 75% of wild-type controls, in the number of large trigeminal motoneurons, whereas normal numbers were found for sensory mesencephalic trigeminal, facial, and trochlear motoneurons. The morphology of many surviving large trigeminal motoneurons was substantially altered, in particular the size and length of perpendicularly extending primary dendrites, but not those of facial or trochlear motoneurons. At the ultrastructural level, proximal dendrites of large trigeminal motoneurons, but not other neurons, were significantly depleted in organelle content such as polyribosomes and showed abnormal (vesiculated) mitochondria. These data indicate primary defects in trigeminal α-motoneurons more than γ-motoneurons. Our findings expand the Loa heterozygote phenotype in two important ways: we reveal dendritic in addition to axonal defects or abnormalities, and we identify the Loa mutation as a mouse model for mixed motor-sensory loss when the entire neuraxis is considered, rather than a model primarily for sensory loss.

摘要

动力蛋白是一种逆行运动蛋白,对于货物在神经元轴突和近端树突中的运输至关重要。已经报道过动力蛋白重链突变 Loa 可导致脊髓运动神经元变性,以及脊髓感觉本体感觉神经元缺陷,但颅神经核受到的关注较少。在这里,我们检查了年轻、成年和老年杂合子 Loa 小鼠颅神经核中神经元的数量和形态,重点是三叉神经、面神经和滑车神经运动核,以及本体感觉中脑三叉神经核。通过使用立体学计数技术,我们报告了大型三叉神经运动神经元数量的缓慢进行性和显著减少,降至野生型对照的 75%,而感觉中脑三叉神经、面神经和滑车神经运动神经元的数量正常。许多存活的大型三叉神经运动神经元的形态发生了很大的改变,特别是垂直延伸的初级树突的大小和长度,但面神经或滑车神经运动神经元的形态没有改变。在超微结构水平上,大型三叉神经运动神经元的近端树突,而不是其他神经元,细胞器含量(如多核糖体)明显减少,并显示出异常的(囊泡化)线粒体。这些数据表明,三叉神经α-运动神经元存在原发性缺陷,而不是 γ-运动神经元。我们的发现以两种重要方式扩展了 Loa 杂合子表型:我们揭示了除轴突缺陷或异常之外的树突缺陷,并且我们将 Loa 突变鉴定为一种混合运动感觉缺失的小鼠模型,当考虑整个轴突时,而不是主要用于感觉缺失的模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c118/3707314/271b010c71a3/nihms485616f1.jpg

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