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多发性硬化症小脑的浦肯野细胞病理学与损失

Purkinje Cell Pathology and Loss in Multiple Sclerosis Cerebellum.

作者信息

Redondo Juliana, Kemp Kevin, Hares Kelly, Rice Claire, Scolding Neil, Wilkins Alastair

机构信息

Multiple Sclerosis and Stem Cell Group, School of Clinical Sciences, University of Bristol, Bristol, UK.

出版信息

Brain Pathol. 2015 Nov;25(6):692-700. doi: 10.1111/bpa.12230. Epub 2014 Dec 31.

Abstract

Cerebellar ataxia commonly occurs in multiple sclerosis, particularly in chronic progressive disease. Previous reports have highlighted both white matter and grey matter pathological changes within the cerebellum; and demyelination and inflammatory cell infiltrates appear commonly. As Purkinje cell axons are the sole output of the cerebellar cortex, understanding pathologic processes within these cells is crucial to develop strategies to prevent their loss and thus reduce ataxia. We studied pathologic changes occurring within Purkinje cells of the cerebellum. Using immunohistochemic techniques, we found changes in neurofilament phosphorylation states within Purkinje cells, including loss of dephosphorylated neurofilament and increased phosphorylated and hyperphosphorylated neurofilament. We also found Purkinje axonal spheroids and Purkinje cell loss, both of which occurred predominantly within areas of leucocortical demyelination within the cerebellar cortex. These changes have important implications for the study of cerebellar involvement in multiple sclerosis and may help design therapies to reduce the burden of ataxia in the condition.

摘要

小脑共济失调常见于多发性硬化症,尤其是在慢性进行性疾病中。先前的报告强调了小脑内白质和灰质的病理变化;脱髓鞘和炎性细胞浸润也很常见。由于浦肯野细胞轴突是小脑皮质的唯一输出,了解这些细胞内的病理过程对于制定预防其丢失从而减少共济失调的策略至关重要。我们研究了小脑浦肯野细胞内发生的病理变化。使用免疫组化技术,我们发现浦肯野细胞内神经丝磷酸化状态发生了变化,包括去磷酸化神经丝的丢失以及磷酸化和过度磷酸化神经丝的增加。我们还发现了浦肯野轴突球和浦肯野细胞丢失,这两者主要发生在小脑皮质白质脱髓鞘区域。这些变化对研究小脑在多发性硬化症中的受累情况具有重要意义,并可能有助于设计疗法以减轻该病中共济失调的负担。

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