1.Phosphorylated TDP-43 Staging of Primary Age-Related Tauopathy.
Xiaoling ZHANG ; Bing SUN ; Xing WANG ; Hui LU ; Fangjie SHAO ; Annemieke J M ROZEMULLER ; Huazheng LIANG ; Chong LIU ; Jiadong CHEN ; Manli HUANG ; Keqing ZHU
Neuroscience Bulletin 2019;35(2):183-192
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 phosphorylated 43-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 ≤ 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.
Aged
;
Aged, 80 and over
;
Aging
;
metabolism
;
pathology
;
Brain
;
metabolism
;
pathology
;
DNA-Binding Proteins
;
metabolism
;
Disease Progression
;
Female
;
Humans
;
Immunohistochemistry
;
Inclusion Bodies
;
pathology
;
Male
;
Middle Aged
;
Neurofibrillary Tangles
;
metabolism
;
pathology
;
Neurons
;
metabolism
;
pathology
;
Severity of Illness Index
;
Tauopathies
;
metabolism
;
pathology