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...

Full description

Bibliographic Details
Main Authors: Keqing Zhu, Xin Wang, Bing Sun, Juanli Wu, Hui Lu, Xiaoling Zhang, Huazheng Liang, Dandan Zhang, Chong Liu
Format: Article
Language:English
Published: Frontiers Media S.A. 2019-05-01
Series:Frontiers in Neuroscience
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fnins.2019.00529/full
id doaj-3d47f35c31454ca691174be095b4a23e
record_format Article
collection 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
work_keys_str_mv AT keqingzhu primaryagerelatedtauopathyinhumansubcorticalnuclei
AT keqingzhu primaryagerelatedtauopathyinhumansubcorticalnuclei
AT xinwang primaryagerelatedtauopathyinhumansubcorticalnuclei
AT xinwang primaryagerelatedtauopathyinhumansubcorticalnuclei
AT bingsun primaryagerelatedtauopathyinhumansubcorticalnuclei
AT juanliwu primaryagerelatedtauopathyinhumansubcorticalnuclei
AT huilu primaryagerelatedtauopathyinhumansubcorticalnuclei
AT xiaolingzhang primaryagerelatedtauopathyinhumansubcorticalnuclei
AT huazhengliang primaryagerelatedtauopathyinhumansubcorticalnuclei
AT huazhengliang primaryagerelatedtauopathyinhumansubcorticalnuclei
AT dandanzhang primaryagerelatedtauopathyinhumansubcorticalnuclei
AT chongliu primaryagerelatedtauopathyinhumansubcorticalnuclei
AT chongliu primaryagerelatedtauopathyinhumansubcorticalnuclei
_version_ 1725359996242231296
spelling 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