Primary Age-Related Tauopathy in Human Subcortical Nuclei
The present study aimed to determine the spatial distribution patterns of hyperphosphorylated tau-immunoreactive cells in subcortical nuclei of post-mortem human brain with primary age-related tauopathy (PART). Subcortical tauopathy has important pathological and clinical implications. Expression of...
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Frontiers Media S.A.
2019-05-01
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Series: | Frontiers in Neuroscience |
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Online Access: | https://www.frontiersin.org/article/10.3389/fnins.2019.00529/full |
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Article |
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DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Keqing Zhu Keqing Zhu Xin Wang Xin Wang Bing Sun Juanli Wu Hui Lu Xiaoling Zhang Huazheng Liang Huazheng Liang Dandan Zhang Chong Liu Chong Liu |
spellingShingle |
Keqing Zhu Keqing Zhu Xin Wang Xin Wang Bing Sun Juanli Wu Hui Lu Xiaoling Zhang Huazheng Liang Huazheng Liang Dandan Zhang Chong Liu Chong Liu Primary Age-Related Tauopathy in Human Subcortical Nuclei Frontiers in Neuroscience primary age-related tauopathy subcortical nuclei Alzheimer’s disease neurofibrillary tangle brainstem brain bank |
author_facet |
Keqing Zhu Keqing Zhu Xin Wang Xin Wang Bing Sun Juanli Wu Hui Lu Xiaoling Zhang Huazheng Liang Huazheng Liang Dandan Zhang Chong Liu Chong Liu |
author_sort |
Keqing Zhu |
title |
Primary Age-Related Tauopathy in Human Subcortical Nuclei |
title_short |
Primary Age-Related Tauopathy in Human Subcortical Nuclei |
title_full |
Primary Age-Related Tauopathy in Human Subcortical Nuclei |
title_fullStr |
Primary Age-Related Tauopathy in Human Subcortical Nuclei |
title_full_unstemmed |
Primary Age-Related Tauopathy in Human Subcortical Nuclei |
title_sort |
primary age-related tauopathy in human subcortical nuclei |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Neuroscience |
issn |
1662-453X |
publishDate |
2019-05-01 |
description |
The present study aimed to determine the spatial distribution patterns of hyperphosphorylated tau-immunoreactive cells in subcortical nuclei of post-mortem human brain with primary age-related tauopathy (PART). Subcortical tauopathy has important pathological and clinical implications. Expression of tau was examined in different subcortical regions of definite PART cases with a Braak neurofibrillary tangle stage >0 and ≤IV, and with a Thal phase 0 (no beta-amyloid present). Post-mortem brain tissue of PART was studied using immunohistochemistry and subsequent semi-quantitative assessment with Braak NFT stage -matched pre-Alzheimer’s disease (AD) and AD cases as a control. Expression of tau was frequently found in subcortical nuclei including the substantia nigra, inferior colliculus, locus coeruleus, medulla oblongata in the brainstem, the caudate, putamen, nucleus globus pallidus in the striatum, the hypothalamus, thalamus, subthalamus in the diencephalon, and the cervical spinal cord in both PART and AD, but not in the dentate nucleus of the cerebellum. A positive correlation was found between the Braak NFT stage and the tau distribution (qualitative)/tau density (quantitative) in PART and AD. Brainstem nuclei were commonly involved in early PART with NFT Braak stage I/II, there was no preference among the substantia nigra, inferior colliculus, locus caeruleus and medulla oblongata. The prevalence and severity of tau pathology in subcortical nuclei of PART and AD were positively correlated with NFT Braak stage, suggesting that these nuclei were increasingly involved as PART and AD progressed. Subcortical nuclei were likely the sites initially affected by aging associated tau pathology, especially the brainstem nuclei including the substantia nigra, inferior colliculus, locus caeruleus and medulla oblongata. |
topic |
primary age-related tauopathy subcortical nuclei Alzheimer’s disease neurofibrillary tangle brainstem brain bank |
url |
https://www.frontiersin.org/article/10.3389/fnins.2019.00529/full |
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doaj-3d47f35c31454ca691174be095b4a23e2020-11-25T00:22:24ZengFrontiers Media S.A.Frontiers in Neuroscience1662-453X2019-05-011310.3389/fnins.2019.00529425965Primary Age-Related Tauopathy in Human Subcortical NucleiKeqing Zhu0Keqing Zhu1Xin Wang2Xin Wang3Bing Sun4Juanli Wu5Hui Lu6Xiaoling Zhang7Huazheng Liang8Huazheng Liang9Dandan Zhang10Chong Liu11Chong Liu12China Brain Bank and Department of Neurology in Second Affiliated Hospital, Key Laboratory of Medical Neurobiology of Zhejiang Province, and Department of Neurobiology, Zhejiang University School of Medicine, Hangzhou, ChinaDepartment of Pathology, Zhejiang University School of Medicine, Hangzhou, ChinaChina Brain Bank and Department of Neurology in Second Affiliated Hospital, Key Laboratory of Medical Neurobiology of Zhejiang Province, and Department of Neurobiology, Zhejiang University School of Medicine, Hangzhou, ChinaDepartment of Pathology, Zhejiang University School of Medicine, Hangzhou, ChinaChina Brain Bank and Department of Neurology in Second Affiliated Hospital, Key Laboratory of Medical Neurobiology of Zhejiang Province, and Department of Neurobiology, Zhejiang University School of Medicine, Hangzhou, ChinaChina Brain Bank and Department of Neurology in Second Affiliated Hospital, Key Laboratory of Medical Neurobiology of Zhejiang Province, and Department of Neurobiology, Zhejiang University School of Medicine, Hangzhou, ChinaChina Brain Bank and Department of Neurology in Second Affiliated Hospital, Key Laboratory of Medical Neurobiology of Zhejiang Province, and Department of Neurobiology, Zhejiang University School of Medicine, Hangzhou, ChinaChina Brain Bank and Department of Neurology in Second Affiliated Hospital, Key Laboratory of Medical Neurobiology of Zhejiang Province, and Department of Neurobiology, Zhejiang University School of Medicine, Hangzhou, ChinaBrain Structure and Function, Neuroscience Research Australia, Randwick, NSW, AustraliaDepartment of Neurology, Shanghai Fourth People’s Hospital, Tongji University, Shanghai, ChinaDepartment of Pathology, Zhejiang University School of Medicine, Hangzhou, ChinaChina Brain Bank and Department of Neurology in Second Affiliated Hospital, Key Laboratory of Medical Neurobiology of Zhejiang Province, and Department of Neurobiology, Zhejiang University School of Medicine, Hangzhou, ChinaDepartment of Pathology, Zhejiang University School of Medicine, Hangzhou, ChinaThe present study aimed to determine the spatial distribution patterns of hyperphosphorylated tau-immunoreactive cells in subcortical nuclei of post-mortem human brain with primary age-related tauopathy (PART). Subcortical tauopathy has important pathological and clinical implications. Expression of tau was examined in different subcortical regions of definite PART cases with a Braak neurofibrillary tangle stage >0 and ≤IV, and with a Thal phase 0 (no beta-amyloid present). Post-mortem brain tissue of PART was studied using immunohistochemistry and subsequent semi-quantitative assessment with Braak NFT stage -matched pre-Alzheimer’s disease (AD) and AD cases as a control. Expression of tau was frequently found in subcortical nuclei including the substantia nigra, inferior colliculus, locus coeruleus, medulla oblongata in the brainstem, the caudate, putamen, nucleus globus pallidus in the striatum, the hypothalamus, thalamus, subthalamus in the diencephalon, and the cervical spinal cord in both PART and AD, but not in the dentate nucleus of the cerebellum. A positive correlation was found between the Braak NFT stage and the tau distribution (qualitative)/tau density (quantitative) in PART and AD. Brainstem nuclei were commonly involved in early PART with NFT Braak stage I/II, there was no preference among the substantia nigra, inferior colliculus, locus caeruleus and medulla oblongata. The prevalence and severity of tau pathology in subcortical nuclei of PART and AD were positively correlated with NFT Braak stage, suggesting that these nuclei were increasingly involved as PART and AD progressed. Subcortical nuclei were likely the sites initially affected by aging associated tau pathology, especially the brainstem nuclei including the substantia nigra, inferior colliculus, locus caeruleus and medulla oblongata.https://www.frontiersin.org/article/10.3389/fnins.2019.00529/fullprimary age-related tauopathysubcortical nucleiAlzheimer’s diseaseneurofibrillary tanglebrainstembrain bank |