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Morphological characterisation of glial and neuronal tau pathology in globular glial tauopathy (Types II and III)

Authors :
H. Otsu
Shinobu Kawakatsu
Kazuhiro Sanpei
Yasuko Toyoshima
Akiyoshi Kakita
Seishi Terada
Osamu Onodera
Hoyu Takahashi
Koichi Otani
Takeshi Ikeuchi
Hirosato Tanaka
Osamu Yokota
Ryota Kobayashi
Yo Higuchi
Miura Takeshi
Shigetoshi Kuroda
Source :
Neuropathology and Applied Neurobiology. 46:344-358
Publication Year :
2019
Publisher :
Wiley, 2019.

Abstract

Aims Globular glial tauopathy (GGT) is a new category within the 4-repeat tauopathies that is characterised neuropathologically by tau-positive globular glial inclusions (GGIs), namely, globular oligodendrocytic and astrocytic inclusions (GOIs and GAIs). Occurrence of tau-positive neuronal cytoplasmic inclusions (NCIs) is also a feature. GGT is classified into three pathological subtypes (Types I, II and III). We studied the tau pathology in 6 cases of GGT (Type II, n = 3; Type III, n = 3), with special reference to GAIs and NCIs. Methods Neuropathological examinations were conducted, along with immunohistochemistry, morphometry and three-dimensional imaging, and biochemical and genetic analysis of tau. Results The cortical GAIs in Type II and those in Type III were distinguishable from each other. In the motor cortex, GAIs were much more numerous in Type III than in Type II. Prominent occurrence of perikaryal globular structures was a feature of GAIs in Type III. By contrast, prominent occurrence of radiating process-like structures was a feature of GAIs in Type II. Overall, the GAIs were significantly smaller in Type III than in Type II. NCIs were divisible into three subgroups in terms of shape: diffuse granular, thick cord-like, and round/horseshoe-shaped structures. In all cases, NCIs were a feature of the upper and lower motor neurons. Interestingly, the round/horseshoe-shaped NCIs were observed only in Type III cases. Conclusions These findings, which characterised GAIs and NCIs, indicated that Type II and Type III constitute two distinct pathological subtypes, and also further strengthen the concept of GGT as a distinct entity.

Details

ISSN :
13652990 and 03051846
Volume :
46
Database :
OpenAIRE
Journal :
Neuropathology and Applied Neurobiology
Accession number :
edsair.doi.dedup.....d1c69563cb9dceb7ee3c07aba4b3dc20
Full Text :
https://doi.org/10.1111/nan.12581