Determination of the receptor type protein tyrosine phosphatase of to the oligodendrocyte differentiation
Project/Area Number |
26830050
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Research Category |
Grant-in-Aid for Young Scientists (B)
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Allocation Type | Multi-year Fund |
Research Field |
Neurochemistry/Neuropharmacology
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Research Institution | National Institute for Basic Biology |
Principal Investigator |
KUBOYAMA Kazuya 基礎生物学研究所, 統合神経生物学研究部門, 特別協力研究員 (20619671)
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Project Period (FY) |
2014-04-01 – 2016-03-31
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Project Status |
Completed (Fiscal Year 2015)
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Budget Amount *help |
¥3,900,000 (Direct Cost: ¥3,000,000、Indirect Cost: ¥900,000)
Fiscal Year 2015: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
Fiscal Year 2014: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
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Keywords | 神経科学 / タンパク質チロシンリン酸化シグナル / チロシンホスファターゼ / オリゴデンドロサイト / 脱髄疾患 / グリア細胞 / 脳・神経 / プロテインチロシンホスファターゼ / チロシンリン酸化 |
Outline of Final Research Achievements |
The purpose of this study was to determine the regulatory mechanism of protein tyrosine phosphatase receptor type Z (PTPRZ), which inhibits oligodendrocyte differentiation and myelination/remyelination. Here we revealed that the expression of pleiotrophin is transiently upregulated in damaged neurons after demyelination. Pleiotrophin may be released from demyelinated axons and bind to PTPRZ at the cell surface of oligodendrocyte precursor cells, thereby releases the block of differentiation into oligodendrocyte, so the remyelination of neighboring axon is initiated.
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Report
(3 results)
Research Products
(12 results)
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[Journal Article] Small-molecule inhibition of PTPRZ reduces tumor growth in a rat model of glioblastoma.2016
Author(s)
Fujikawa A, Nagahira A, Sugawara H, Ishii K, Imajo S, Matsumoto M, Kuboyama K, Suzuki R, Tanga N, Noda M, Uchiyama S, Tomoo T, Ogata A, Masumura M, Noda M.
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Journal Title
Sci Rep.
Volume: 6
Issue: 1
Pages: 20473-20473
DOI
Related Report
Peer Reviewed / Open Access
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[Journal Article] Loss of Function Mutation in APC2 Causes Sotos Syndrome Features.2015
Author(s)
Almuriekhi, M., Shintani, T., Fahiminiya, S., Fujikawa, A., Kuboyama, K., Takeuchi, Y., Nawaz, Z., Nadaf, J., Kamel, H., Kitam, A.K., Samiha, Z., Mahmoud, L., Ben-Omran, T., Majewski, J. & Noda, M.
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Journal Title
Cell Reports
Volume: 10
Issue: 9
Pages: 1585-1598
DOI
Related Report
Peer Reviewed / Open Access / Acknowledgement Compliant
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[Presentation] Loss-of-Function Mutation in APC2 Causes Sotos Syndrome Features.2015
Author(s)
新谷隆史, Fahiminiya S, Almuriekhi M, 藤川顕寛, 久保山和哉, 竹内靖, Nawaz Z, Nadaf J, Kamel H, Kitam KA, Samiha Z, Mahmoud L, Ben-Omran T, Majewski J, 野田昌晴
Organizer
第38回 日本神経科学大会
Place of Presentation
神戸国際会議場(兵庫県神戸市)
Year and Date
2015-07-28
Related Report
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