| Project/Area Number |
15H04270
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| Research Category |
Grant-in-Aid for Scientific Research (B)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Nerve anatomy/Neuropathology
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| Research Institution | Wakayama Medical University |
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Principal Investigator |
Ito Hidefumi 和歌山県立医科大学, 医学部, 教授 (20250061)
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| Co-Investigator(Kenkyū-buntansha) |
紀平 為子 関西医療大学, 保健医療学部, 教授 (30225015)
中山 宜昭 和歌山県立医科大学, 医学部, その他 (50590436)
綾木 孝 京都大学, 医学研究科, 特定病院助教 (60749555)
廣西 昌也 和歌山県立医科大学, 医学部, 講師 (80316116)
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| Co-Investigator(Renkei-kenkyūsha) |
ISHIGUCHI Hiroshi 和歌山県立医科大学, 医学部, 博士研究員 (70389443)
KAWAKAMI Hideshi 広島大学, 原爆放射線医科学研究所, 教授 (70253060)
TAKAHASHI Ryosuke 京都大学, 医学部, 教授 (90216771)
INOUE Haruhisa 京都大学, 医学部, 教授 (70332327)
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| Project Period (FY) |
2015-04-01 – 2018-03-31
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| Project Status |
Completed (Fiscal Year 2017)
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| Budget Amount *help |
¥17,810,000 (Direct Cost: ¥13,700,000、Indirect Cost: ¥4,110,000)
Fiscal Year 2017: ¥5,200,000 (Direct Cost: ¥4,000,000、Indirect Cost: ¥1,200,000)
Fiscal Year 2016: ¥5,980,000 (Direct Cost: ¥4,600,000、Indirect Cost: ¥1,380,000)
Fiscal Year 2015: ¥6,630,000 (Direct Cost: ¥5,100,000、Indirect Cost: ¥1,530,000)
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| Keywords | 筋萎縮性側索硬化症 / パーキンソン認知症複合 / 紀伊半島 / タウタンパク / TDP-43 / ポリユビキチン / 神経科学 / ポリユビキチン鎖 / タンパク分解系 / 神経炎症 / 神経病理 / 遺伝子解析 |
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| Outline of Final Research Achievements |
We compared pathological features of Kii ALS among past cases and present cases. For tau pathology analysis, we examined distribution of NFT and glial cytoplasmic inclusions. In both the past and the present cases, NFT were found in motor cortex, frontal and temporal lobes, hippocampus, amygdala, and furthermore brainstem. NFT were found predominantly in superficial layer of cerebral cortex. In addition, we detected granular hazy inclusions and granular or fuzzy tau immunoreactivity in processes of astrocytes as glial cytoplasmic inclusions in both cases. In TDP-43 pathology analysis, unlike with conventional ALS, neurocytoplasmic inclusions were detected more abundant in hippocampus than basal ganglia in both cases.
These features of tau pathology and TDP-43 pathology were consistent in both past and present cases. Consequently, it is supposed that the basic pathological features of Kii ALS did not change through the change of living environment.
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