| Project/Area Number |
16590184
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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 |
Environmental physiology (including Physical medicine and Nutritional physiology)
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| Research Institution | Kinki University |
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Principal Investigator |
HAYASAKA Naoto Kinki University, School of Medicine, Assistant Professor, 医学部, 助手 (80368290)
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| Co-Investigator(Kenkyū-buntansha) |
SHIGEYOSHI Yasufumi Kinki University, School of Medicine, Professor, 医学部, 教授 (20275192)
NAGANO Mamoru Kinki University, School of Medicine, Lecturer, 医学部, 講師 (80155960)
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| Project Period (FY) |
2004 – 2005
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| Project Status |
Completed (Fiscal Year 2005)
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| Budget Amount *help |
¥3,100,000 (Direct Cost: ¥3,100,000)
Fiscal Year 2005: ¥1,200,000 (Direct Cost: ¥1,200,000)
Fiscal Year 2004: ¥1,900,000 (Direct Cost: ¥1,900,000)
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| Keywords | Neuroscience / Brain, Neuron / Circadian clock / Gene function / ウイルス / 視交叉上核 / 概日リズム / Rgs16 / レンチウイルス / Hmg4 / RNAi / スライスカルチャー / 肝臓 |
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| Research Abstract |
We have previously identified circadianly regulated genes in the suprachiasmatic nucleus (SCN) and liver by Gene Chip analyses. To elucidate their functions in efficient and multidimensional ways, we have established methods using a lentiviral vector system to analyze gene functions both in vivo and in vitro. First, we constructed lentiviral vectors for overexpression or knockdown (siRNA) of candidate genes. Then we developed a technique to inject lentivirus into the mouse SCN using a stereotaxic instrument with a syringe pump. The method enabled us to analyze circadian phenotype (e.g., locomotor activity) in vivo right after injection of the virus in the SCN and made it possible to analyze functions of several candidate genes in a short term. Next, we further applied the virus infection to brain slices. We established a method to efficiently introduce a transgene into the SCN, which had been quite difficult like in other tissues. Using this new method, we studied roles of the candidate genes in circadian system by measuring different circadian outputs. By making SCN slices from transgenic rats/mice carrying Per2::luciferase, which demonstrate circadian rhythmicity of luciferase activity, we examine an effect of the candidate gene expression on the circadian rhythms of the Per2::luc. We also analyzed circadian activity of the SCN neurons in the same slices by electrophysiology. Lastly, we could also study roles of the candidate genes using dissociated neurons/glias infected with the lentivirus. Using these methods mentioned above, so far we have analyzed two candidate genes, Rgs16 and Hmg4 and are preparing to publish papers
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