Molecular basis for stress vulnerability of hippocampal newborn neurons derived from GFAP-expressing stem cells
| Project/Area Number |
22500313
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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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 | Fukushima Medical University (2011-2013)
Kyoto Prefectural University of Medicine (2010) |
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Principal Investigator |
IMURA Tetsuya 福島県立医科大学, 医学部, 准教授 (00405276)
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| Project Period (FY) |
2010-04-01 – 2013-03-31
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| Project Status |
Completed (Fiscal Year 2013)
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| Budget Amount *help |
¥4,420,000 (Direct Cost: ¥3,400,000、Indirect Cost: ¥1,020,000)
Fiscal Year 2012: ¥910,000 (Direct Cost: ¥700,000、Indirect Cost: ¥210,000)
Fiscal Year 2011: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Fiscal Year 2010: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
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| Keywords | 神経幹細胞 / 神経新生 / 老化 / ストレス / 再生医学 / 脳・神経 / 神経科学 |
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| Research Abstract |
New neurons in the adult brain are originated from GFAP-expressing neural stem cells (GFAP+NSCs). In the present study, we analyzed the dynamic properties of GFAP+NSC-derived new granule cells (GCs) in the hippocampal dentate gyrus with reference to aging and stress vulnerability.
The contribution of GFAP+NSC-derived GCs to the whole GC layer in mice sharply increased during the juvenile period followed by a subtle addition by old age, which was variable depending on spatial positioning and sex. The survival of newborn neurons was deteriorated by the chronic environmental stress , but there was a critical period of vulnerability for the stress during their differentiation. We also performed a comprehensive analysis of the gene expression profiles in the GC layer and found several candidate molecules implicated in the regulation of adult-born GCs.
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Report
(4 results)
Research Products
(3 results)
