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Detection of hyperphosphorylated tau protein and alpha-synuclein in spinal cord of patients with Alzheimer's disease

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机构: [1]Department of Neurology, Beijing Friendship Hospital, Capital Medical University [2]Department of Geriatric Neurology, PLA General Hospital [3]Institute of Geriatrics, Chinese PLA General Hospital & Chinese PLA Medical Academy [4]Department of Neurology, Xuanwu Hospital, Capital Medical University, Beijing, People’s Republic of China
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关键词: Alzheimer's disease alpha-synuclein tau protein neurofibrillary tangles histopathology

摘要:
The aim of this study was to investigate the neuropathological features of the spinal cord in patients suffering with Alzheimer's disease (AD). Spinal cord tissue collected from three AD patients and eight controls was selected for the study. Data were collected at T2, T8, T10, L4, and S2 spinal levels. The sections were subjected to hematoxylin and eosin and Gallyas-Braak staining methods and then were immunostained with antibodies such as phosphorylated tau protein (AT8), alpha-synuclein, A beta, amyloid precursor protein, ubiquitin, and TDP-43. Pathological changes exhibited by the biomarkers were detected by microscopy. Neurofibrillary tangles (NFTs) were detectable in spinal anterior horn motor neurons in two of the three AD patients. AT8-positive axons or axon-like structures and AT8 expression in glial cells were detected in all three AD cases. Hyperphosphorylation of tau protein was detected in spinal anterior horn cells, glial cells, and axons, and its severity was associated with NFTs in the brain tissue. alpha-Synuclein-positive Lewy bodies and scattered Lewy-like neuritis were detected in the medial horn of the thoracic spinal cord and ventral sacral gray matter, respectively, in one patient who had AD with Lewy bodies. Neither amyloid deposition nor amyloid precursor protein and TDP-43 expression was detected in the spinal cord of AD patients. Spinal cord of AD patients was observed to contain phosphorylated tau protein and alpha-synuclein immunoreactive structures, which may play a role in dyskinesia and autonomic dysfunction in advanced AD.

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出版当年[2015]版:
大类 | 4 区 医学
小类 | 4 区 临床神经病学 4 区 精神病学
最新[2023]版:
大类 | 3 区 医学
小类 | 4 区 临床神经病学 4 区 精神病学
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出版当年[2014]版:
Q3 CLINICAL NEUROLOGY Q3 PSYCHIATRY
最新[2023]版:
Q2 CLINICAL NEUROLOGY Q2 PSYCHIATRY

影响因子: 最新[2023版] 最新五年平均 出版当年[2014版] 出版当年五年平均 出版前一年[2013版] 出版后一年[2015版]

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第一作者机构: [1]Department of Neurology, Beijing Friendship Hospital, Capital Medical University [2]Department of Geriatric Neurology, PLA General Hospital
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通讯机构: [2]Department of Geriatric Neurology, PLA General Hospital [*1]Department of Geriatric Neurology, PLA General Hospital, 28 Fuxing Road, Haidian District, Beijing 100853, People’s Republic of China
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