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散发性运动神经元病中脊髓腹角神经元群体的广泛缺失。一项形态计量学研究。

Widespread loss of neuronal populations in the spinal ventral horn in sporadic motor neuron disease. A morphometric study.

作者信息

Stephens Benjamin, Guiloff Roberto J, Navarrete Roberto, Newman Piers, Nikhar Nirjal, Lewis Paul

机构信息

Neuromuscular Unit, West London Neurosciences Centre, Imperial College London, UK.

出版信息

J Neurol Sci. 2006 May 15;244(1-2):41-58. doi: 10.1016/j.jns.2005.12.003. Epub 2006 Feb 17.

DOI:10.1016/j.jns.2005.12.003
PMID:16487542
Abstract

The cytopathology and loss of neurons was studied in 7670 neurons from the ventral horn of the third lumbar segment of the spinal cord of six sporadic motor neuron disease (MND) patients compared with 7568 neurons in seven age matched control subjects. A modified Tomlinson et al. [Tomlinson BE, Irving D, Rebeiz JJ. Total numbers of limb motor neurones in the human lumbosacral cord and an analysis of the accuracy of various sampling procedures. J Neurol Sci 1973;20:313-27] sampling procedure was used for neuronal counts. The ventral horn was divided in quadrants. Neuronal populations were also classified by the maximum cell diameter through the nucleolus. There was widespread loss of neurons in all quadrants of the ventral horn in MND. Size distribution histograms showed similar neuron loss across all populations of neurons. The dorsomedial quadrant contains almost exclusively interneurons and the ventrolateral quadrant mostly motor neurons. The cytopathology of neurons in the dorsomedial quadrant and of large motorneurons in the ventrolateral quadrant MND was similar. In the dorsomedial quadrant, neuron loss (56.7%) was similar to the loss of large motor neurons in the ventrolateral quadrant (64.4%). The loss of presumed motor neurons and interneurons increased with increased disease duration. There was no evidence that loss of presumed interneurons occurred prior, or subsequent, to loss of motor neurons. We conclude that, in sporadic MND, all neuronal populations in the ventral horn are affected and that interneurons are involved to a similar extent and in parallel with motor neurons, as reported in the G86R transgenic mouse model of familial MND. The increasing evidence of loss of neurons other than motor neurons in MND suggests the need for revising the concept of selective motor neuron vulnerability.

摘要

对6例散发性运动神经元病(MND)患者第三腰椎节段脊髓腹角的7670个神经元进行了细胞病理学和神经元丢失情况研究,并与7例年龄匹配的对照受试者的7568个神经元进行对比。采用改良的汤姆林森等人[汤姆林森BE、欧文D、雷贝兹JJ。人类腰骶部脊髓肢体运动神经元总数及各种采样程序准确性分析。《神经科学杂志》1973年;20:313 - 27]的采样程序进行神经元计数。腹角被划分为象限。神经元群体也根据穿过核仁的最大细胞直径进行分类。MND患者腹角所有象限均存在广泛的神经元丢失。大小分布直方图显示所有神经元群体的神经元丢失情况相似。背内侧象限几乎只包含中间神经元,腹外侧象限大多是运动神经元。MND患者背内侧象限神经元和腹外侧象限大型运动神经元的细胞病理学相似。在背内侧象限,神经元丢失率(56.7%)与腹外侧象限大型运动神经元的丢失率(64.4%)相似。推测的运动神经元和中间神经元的丢失随疾病持续时间增加而增多。没有证据表明推测的中间神经元的丢失先于或后于运动神经元的丢失。我们得出结论,在散发性MND中,腹角的所有神经元群体均受影响,并且中间神经元与运动神经元受到相似程度的累及且是并行的,这与家族性MND的G86R转基因小鼠模型中的报道一致。MND中运动神经元以外的神经元丢失的证据不断增加,提示需要修订选择性运动神经元易损性的概念。

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