Project/Area Number |
26430052
|
Research Category |
Grant-in-Aid for Scientific Research (C)
|
Allocation Type | Multi-year Fund |
Section | 一般 |
Research Field |
Nerve anatomy/Neuropathology
|
Research Institution | Niigata University |
Principal Investigator |
|
Co-Investigator(Kenkyū-buntansha) |
池内 健 新潟大学, 脳研究所, 教授 (20372469)
他田 真理 新潟大学, 脳研究所, 助教 (30646394)
高橋 均 新潟大学, 脳研究所, 教授 (90206839)
|
Project Period (FY) |
2014-04-01 – 2017-03-31
|
Project Status |
Completed (Fiscal Year 2016)
|
Budget Amount *help |
¥5,070,000 (Direct Cost: ¥3,900,000、Indirect Cost: ¥1,170,000)
Fiscal Year 2016: ¥1,170,000 (Direct Cost: ¥900,000、Indirect Cost: ¥270,000)
Fiscal Year 2015: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Fiscal Year 2014: ¥2,210,000 (Direct Cost: ¥1,700,000、Indirect Cost: ¥510,000)
|
Keywords | タウオパチー / アストロサイト / globular glial tauopathy / オリゴマー / 神経変性疾患 / ピック病 / タウオリゴマー / 進行性核上性麻痺 |
Outline of Final Research Achievements |
We examined the brains of GGT-type III, using an anti-tau oligomer-specific polyclonal antibody, T22 and anti-phosphorylated tau antibody, AT8. Predominant occurrence of GAIs was also confirmed with AT8 and T22. We consider that GGT are different from other 4R tauopathies not only in their pathological picture but also in their constituent tau species. It is tempting to speculate that GAIs represent a distinct, 4R tau-oligomer astrocytopathy that characterizes GGT. We also performed a pathological and clinical investigation in 40 consecutive autopsied patients with pathological diagnoses of PSP-related disease. Unequivocal TAs were present in 22 cases, all of which were confirmed to be PSP. Such TAs were hardly observed in the other 18 cases. Cluster analysis of the distribution pattern of tau-related pathology for these 18 cases identified two subgroups, pallido-nigro-luysian atrophy (PNLA) Type 1 (n = 9) and Type 2 (n = 9).
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