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論文
タイトル
タイトル(英)
Factors associated with development and distribution of granular/fuzzy astrocytes in neurodegenerative diseases
参照URL
https://researchmap.jp/masatohasegawa/published_papers/34661910
著者
著者(英)
Tomoko Miki,Osamu Yokota,Takashi Haraguchi,Hideki Ishizu,Masato Hasegawa,Takeshi Ishihara,Shu-ichi Ueno,Shintaro Takenoshita,Seishi Terada,Norihito Yamada
担当区分
概要
概要(英)
Granular/fuzzy astrocytes (GFAs), a subtype of "aging-related tau astrogliopathy," are noted in cases bearing various neurodegenerative diseases. However, the pathogenic significance of GFAs remains unclear. We immunohistochemically examined the frontal cortex, caudate nucleus, putamen and amygdala in 105 cases composed of argyrophilic grain disease cases (AGD, N = 26), and progressive supranuclear palsy (PSP, N = 10), Alzheimer's disease (AD, N = 20) and primary age-related tauopathy cases (PART, N = 18) lacking AGD, as well as 31 cases bearing other various neurodegenerative diseases to clarify (i) the distribution patterns of GFAs in AGD, and PSP, AD and PART lacking AGD, (ii) the impacts of major pathological factors and age on GFA formation and (iii) immunohistochemical features useful to understand the formation process of GFAs. In AGD cases, GFAs consistently occurred in the amygdala (100%), followed by the putamen (69.2%) and caudate nucleus and frontal cortex (57.7%, respectively). In PSP cases without AGD, GFAs were almost consistently noted in all regions examined (90-100%). In AD cases without AGD, GFAs were less frequent, developing preferably in the putamen (35.0%) and caudate nucleus (30.0%). PART cases without AGD had GFAs most frequently in the amygdala (35.3%), being more similar to AGD than to AD cases. Ordered logistic regression analyses using all cases demonstrated that the strongest independent factor of GFA formation in the frontal cortex and striatum was the diagnosis of PSP, while that in the amygdala was AGD. The age was not significantly associated with GFA formation in any region. In GFAs in AGD cases, phosphorylation and conformational change of tau, Gallyas-positive glial threads indistinguishable from those in tufted astrocytes, and the activation of autophagy occurred sequentially. Given these findings, AGD, PSP, AD and PART cases may show distinct distributions of GFAs, which may provide clues to predict the underlying processes of primary tauopathies.
出版者・発行元
出版者・発行元(英)
WILEY
誌名
誌名(英)
BRAIN PATHOLOGY
30
4
開始ページ
811
終了ページ
830
出版年月
2020年7月
査読の有無
招待の有無
掲載種別
研究論文(学術雑誌)
ISSN
1015-6305
DOI URL
https://doi.org/10.1111/bpa.12843
共同研究・競争的資金等の研究課題
研究者