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首页> 外文期刊>Brain pathology >Synaptic pathology in the cerebellar dentate nucleus in chronic multiple sclerosis
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Synaptic pathology in the cerebellar dentate nucleus in chronic multiple sclerosis

机译:慢性多发性硬化症中小脑牙齿细胞核中的突触病理

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摘要

Abstract In multiple sclerosis, cerebellar symptoms are associated with clinical impairment and an increased likelihood of progressive course. Cortical atrophy and synaptic dysfunction play a prominent role in cerebellar pathology and although the dentate nucleus is a predilection site for lesion development, structural synaptic changes in this region remain largely unexplored. Moreover, the mechanisms leading to synaptic dysfunction have not yet been investigated at an ultrastructural level in multiple sclerosis. Here, we report on synaptic changes of dentate nuclei in post‐mortem cerebella of 16 multiple sclerosis patients and eight controls at the histological level as well as an electron microscopy evaluation of afferent synapses of the cerebellar dentate and pontine nuclei of one multiple sclerosis patient and one control. We found a significant reduction of afferent dentate synapses in multiple sclerosis, irrespective of the presence of demyelination, and a close relationship between glial processes and dentate synapses. Ultrastructurally, we show autophagosomes containing degradation products of synaptic vesicles within dendrites, residual bodies within intact‐appearing axons and free postsynaptic densities opposed to astrocytic appendages. Our study demonstrates loss of dentate afferent synapses and provides, for the first time, ultrastructural evidence pointing towards neuron‐autonomous and neuroglia‐mediated mechanisms of synaptic degradation in chronic multiple sclerosis.
机译:摘要在多发性硬化症中,小脑症状与临床损害有关,增加了进步课程的可能性。皮质萎缩和突触功能障碍在小脑病理学中发挥着突出的作用,尽管牙齿核是病变发展的偏好现场,但该地区的结构突触变化仍然很大程度上是未开发的。此外,尚未在多发性硬化的超微结构水平下研究导致突触功能障碍的机制。在这里,我们报告了16例多发性硬化症患者的验尸小核诱导核的突触变化和组织学水平的八种对照,以及一种多发性硬化患者的小脑齿状牙齿和猪核的传入突触的电子显微镜评价一个控制。我们发现多发性硬化症中传入牙齿突触的显着减少,无论脱髓鞘的存在,以及胶质过程与牙齿突触之间的密切关系。超微结构,我们显示含有树突内突触囊泡的突触囊泡的降解产物的自噬体,完整出现的轴突内的残余体和与星形胶质细胞阑尾的自由突触密度。我们的研究表明,牙齿传入突触的丧失,并在首次提供了超微结构证据,指向神经元 - 自主和神经胶质细胞介导的突触患者中慢性多发性硬化症中的突触降解机制。

著录项

  • 来源
    《Brain pathology 》 |2017年第6期| 共11页
  • 作者单位

    Department of Neuropathology University Medical Center Robert‐Koch‐Stra?e 40G?ttingen D‐37075;

    Department of Neuropathology University Medical Center Robert‐Koch‐Stra?e 40G?ttingen D‐37075;

    Department of Anatomy University Medical Center Kreuzbergring 36G?ttingen D‐37075 Germany;

    Neuroimmunology unit 3801 University StreetMontreal Canada;

    Department of Neurology Sydney Medical SchoolUniversity of SydneySydney NSW 2006 Australia;

    Department of Anatomy and Human Brain Tissue Bank Tüzoltó utca 58Budapest Hungary;

    Department of Anatomy University Medical Center Kreuzbergring 36G?ttingen D‐37075 Germany;

    Department of Neuropathology University Medical Center Robert‐Koch‐Stra?e 40G?ttingen D‐37075;

    Department of Neuropathology University Medical Center Robert‐Koch‐Stra?e 40G?ttingen D‐37075;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 病理学 ;
  • 关键词

    autophagy; cerebellum; dentate nucleus; multiple sclerosis; synapses;

    机译:自噬;小脑;牙齿细胞核;多发性硬化;突触;

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