A novel immune regulation mechanism by Ca-independent PLA2 and its contribution to neurodegenerative diseases
Project/Area Number |
20390117
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Research Category |
Grant-in-Aid for Scientific Research (B)
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Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
Experimental pathology
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Research Institution | St.Marianna University School of Medicine |
Principal Investigator |
SEINO Ken-Ichiro St.Marianna University School of Medicine, 遺伝子病制御研究所, 教授 (20312845)
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Research Collaborator |
WADA Haruka 北海道大学, 遺伝子病制御研究所, 助教 (70392181)
KOJO Satoshi 北海道大学, 遺伝子病制御研究所, 助教 (70360542)
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Project Period (FY) |
2008 – 2010
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Project Status |
Completed (Fiscal Year 2010)
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Budget Amount *help |
¥19,630,000 (Direct Cost: ¥15,100,000、Indirect Cost: ¥4,530,000)
Fiscal Year 2010: ¥5,720,000 (Direct Cost: ¥4,400,000、Indirect Cost: ¥1,320,000)
Fiscal Year 2009: ¥6,630,000 (Direct Cost: ¥5,100,000、Indirect Cost: ¥1,530,000)
Fiscal Year 2008: ¥7,280,000 (Direct Cost: ¥5,600,000、Indirect Cost: ¥1,680,000)
|
Keywords | 疾患モデル動物 / NKT細胞 / INAD |
Research Abstract |
We have investigated the mutant mice bearing a point mutation in Ca-independent PLA2 (iPLA2・、Pla2g6) . They showed a progressive paralysis in their lower limbs since several weeks after the birth. The mutant mice were realized as model mice of human infantile neuroaxonal dystrophy. The mice also showed some immune abnormality such as increase of NKT cell population. We can use the mutant mice for further investigating the disease mechanism and developing new therapeutic strategies.
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Report
(4 results)
Research Products
(9 results)
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[Journal Article] Establishment of an improved mouse model for infantile neuroaxonal dystrophy bearing a point mutation in Pla2g6 which shows early disease onset.2009
Author(s)
Wada H, Yasuda T, Miura I, Watabe K, Sawa C, Kamijuku H, Kojo S, Taniguchi M, Nishino I, Wakana S, Yoshida H, Seino K.
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Journal Title
Am J Pathol 175
Pages: 2257-63
Related Report
Peer Reviewed
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