Mechanism of aggregation-independent neurotoxicity induced by tau
Project/Area Number |
24700368
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Research Category |
Grant-in-Aid for Young Scientists (B)
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Allocation Type | Multi-year Fund |
Research Field |
Nerve anatomy/Neuropathology
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Research Institution | Doshisha University |
Principal Investigator |
XIE Ce 同志社大学, 生命医科学部, 特別研究員 (10598981)
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Project Period (FY) |
2012 – 2013
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Project Status |
Completed (Fiscal Year 2013)
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Budget Amount *help |
¥4,550,000 (Direct Cost: ¥3,500,000、Indirect Cost: ¥1,050,000)
Fiscal Year 2013: ¥2,340,000 (Direct Cost: ¥1,800,000、Indirect Cost: ¥540,000)
Fiscal Year 2012: ¥2,210,000 (Direct Cost: ¥1,700,000、Indirect Cost: ¥510,000)
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Keywords | タウ / タウオパチー / 認知症 / 線虫 / アクチン |
Research Abstract |
Microtubule-associated protein tau aggregates and deposits in the degenerated neurons of many dementia developed with aging. These diseases are called tauopathies, which mechanism is still unclear. The proteins that associated with the abnormal tau are considered to be deeply related to the neurotoxic mechanism. In this study, we identified the proteins that may be involved in the toxic mechanism of tau, using a C. elegans model, in which abnormal tau was expressed without aggregation formation.
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Report
(3 results)
Research Products
(7 results)
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[Journal Article] The homologous carboxyl-terminal domains of microtubule-associated protein 2 and TAU induce neuronal dysfunction and have differential fates in the evolution of neurofibrillary tangles.2014
Author(s)
Xie, C., T. Miyasaka, S. Yoshimura, H. Hatsuta, S. Yoshina, E. Kage-Nakadai, S. Mitani, Murayama, S., Y. Ihara
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Journal Title
PLoS One
Volume: 9
Issue: 2
Pages: e89796-e89796
DOI
Related Report
Peer Reviewed
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