Functional analysis of ER stress sensor OASIS on the neuronal protection from the toxicity of kainic acid.
Project/Area Number |
21700410
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Research Category |
Grant-in-Aid for Young Scientists (B)
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Allocation Type | Single-year Grants |
Research Field |
Neurochemistry/Neuropharmacology
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Research Institution | University of Fukui |
Principal Investigator |
CHIHARA Kazuyasu University of Fukui, 医学部, 講師 (00314948)
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Project Period (FY) |
2009 – 2010
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Project Status |
Completed (Fiscal Year 2010)
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Budget Amount *help |
¥4,420,000 (Direct Cost: ¥3,400,000、Indirect Cost: ¥1,020,000)
Fiscal Year 2010: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Fiscal Year 2009: ¥2,730,000 (Direct Cost: ¥2,100,000、Indirect Cost: ¥630,000)
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Keywords | グリア細胞 / 小胞体ストレス応答 / 小胞体ストレス / 神経細胞死 / カイニン酸 |
Research Abstract |
Accumulated evidence clearly indicates that ER stress is involved in the development of neurodegenerative disorders including Alzheimer's disease. We have investigated the functions of ER stress sensor OASIS, which is specifically expressed in astrocyte. Recently, we established OASIS-/- mouse which shows the increased vulnerability of hippocampal pyramidal neurons to the toxicity of kainic acid. In this study, we found that OASIS expressed in astrocyte plays important roles on the expression and secretion of brain-derived neurotrophic factor (BDNF) to protect the neurons from the toxicity of kainic acid.
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Report
(3 results)
Research Products
(22 results)
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[Journal Article] Regulation of ER molecular chaperone prevents bone loss in a murine model for osteoporosis.2010
Author(s)
Hino, S.Kondo, S.Yoshinaga, K.Saito, A.Murakami, T.Kanemoto, S.Sekiya, H.Chihara, K.Aikawa, Y.Hara, H.Kudo, T.Sekimoto, T.Funamoto, T.Chosa, E.Imaizumi, K.
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Journal Title
J.Bone Miner.Metab. 28(2)
Pages: 131-138
NAID
Related Report
Peer Reviewed
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[Journal Article] Regulation of ER molecular chaperone prevents bone loss in a murinemodel for osteoporosis.2010
Author(s)
Hino S-I, Kondo S, Yoshinaga K, Saito A, Murakami T, Kanemoto S, Sekiya H, Chihara K, Aikawa Y, Hara H, Kudo T, Sekimoto T, Funamoto T, Chosa E, Imaizumi K
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Journal Title
Journal of Bone and Mineral Metabolism 28(2)
Pages: 131-138
Related Report
Peer Reviewed
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[Journal Article] Signalling mediated by the endoplasmic reticulum stress transducer OASIS is involved in bone formation.2009
Author(s)
Murakami, T.Saito, A.Hino, S.Kondo,S.Kanemoto, S.Chihara, K.Sekiya, H.Tsumagari, K.Ochiai, K.Yoshinaga, K.Saitoh, M.Nishimura, R.Yoneda, T.Kou, I.Furuichi, T.Ikegawa, S.Ikawa, M.Okabe, M.Wanaka, A., Imaizumi, K.
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Journal Title
Nat.Cell Biol. 11(10)
Pages: 1205-1211
Related Report
Peer Reviewed
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[Journal Article] Increased vulnerability of hippocampal pyramidal neurons to the toxicity of kainicacid in OASIS-deficient mice.2009
Author(s)
Chihara, K.Saito, A.Murakami, T.Hino, S.Aoki, Y.Sekiya, H.Aikawa, Y.Wanaka, A., Imaizumi, K.
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Journal Title
J.Neurochem 110(3)
Pages: 956-965
Related Report
Peer Reviewed
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[Journal Article] Signalling mediated by the endoplasmic reticulum stress transducer OASIS is involved in bone formation.2009
Author(s)
Murakami T, Saito A, Hino S-I, Kondo S, Kanemoto S, Chihara K, Sekiya H, Tsumagari K, Ochiai K, Yoshinaga K, Saitoh M, Nishimura R, Yoneda T, Kou I, Furuichi T, Ikegawa S, Ikawa M, Okabe M, Wanaka A, Imaizumi K.
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Journal Title
Nature Cell Biology 11(10)
Pages: 1205-1211
Related Report
Peer Reviewed
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