Phosphorylated TDP-43 Staging of Primary Age-Related Tauopathy

被引:0
作者
Xiaoling Zhang [1 ]
Bing Sun [1 ]
Xing Wang [2 ]
Hui Lu [1 ]
Fangjie Shao [2 ]
Annemieke JMRozemuller [3 ]
Huazheng Liang [4 ]
Chong Liu [1 ,2 ]
Jiadong Chen [1 ]
Manli Huang [5 ]
Keqing Zhu [1 ,2 ]
机构
[1] China Brain Bank and Department of Neurology in Second Affiliated Hospital, Key Laboratory of Medical Neurobiology of Zhejiang Province, Department of Neurobiology, Zhejiang University School of Medicine
[2] Department of Pathology, Zhejiang University School of Medicine
[3] Department of Pathology, Amsterdam Neuroscience, VU University Medical Center
[4] Brain Structure and Function Group, Neuroscience Research Australia
[5] Department of Psychiatry, First Affiliated Hospital, Zhejiang University School of Medicine
关键词
TDP-43; Primary age-related tauopathy; Alzheimer’s disease; Neuro?brillary tangle; Hippocampus;
D O I
暂无
中图分类号
R742 [脑部疾病];
学科分类号
1002 ;
摘要
Primary age-related tauopathy(PART) is characterized by tau neurofibrillary tangles(NFTs) in the absence of amyloid plaque pathology. In the present study,we analyzed the distribution patterns of phosphorylated43-kDa TAR DNA-binding protein(pTDP-43) in the brains of patients with PART. Immunohistochemistry and immunofluorescence double-labeling in multiple brain regions was performed on brain tissues from PART,Alzheimer's disease(AD), and aging control cases. We examined the regional distribution patterns of pTDP-43 intraneuronal inclusions in PART with Braak NFT stages[ 0 and B IV, and a Thal phase of 0(no beta-amyloid present). We found four stages which indicated potentially sequential dissemination of pTDP-43 in PART. Stage I was characterized by the presence of pTDP-43 lesions in the amygdala, stage II by such lesions in the hippocampus,stage III by spread of pTDP-43 to the neocortex, and stage IV by pTDP-43 lesions in the putamen, pallidum, and insular cortex. In general, the distribution pattern of pTDP-43 pathology in PART cases was similar to the early TDP-43 stages reported in AD, but tended to be more restricted to the limbic system. However, there were some differences in the distribution patterns of pTDP-43 between PART and AD, especially in the dentate gyrus of the hippocampus. Positive correlations were found in PART between the Braak NFT stage and the pTDP-43 stage and density.
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页码:183 / 192
页数:10
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