| Project/Area Number |
18K10130
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Multi-year Fund |
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| Section | 一般 |
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| Review Section |
Basic Section 58040:Forensics medicine-related
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| Research Institution | Kumamoto University |
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Principal Investigator |
Nishitani Yoko 熊本大学, 大学院生命科学研究部(医), 教授 (30359997)
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| Project Period (FY) |
2018-04-01 – 2022-03-31
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| Project Status |
Completed (Fiscal Year 2021)
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| Budget Amount *help |
¥3,900,000 (Direct Cost: ¥3,000,000、Indirect Cost: ¥900,000)
Fiscal Year 2020: ¥1,170,000 (Direct Cost: ¥900,000、Indirect Cost: ¥270,000)
Fiscal Year 2019: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2018: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
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| Keywords | アルコール / 初代培養肝細胞 / 細胞同調 / 概日リズム / 日内変動 / コラーゲン培地 / コラーゲンゲル培地 / アセチル化制御 / 脂質代謝 / 肝障害 |
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| Outline of Final Research Achievements |
Ethanol affects the various intracellular signaling. Since ethanol metabolism via ADH (alcohol dehydrogenases) decreases NAD in hepatocyte, depletion of NAD may lead to insufficence of sirtuins that work as NAD-related deacetylation. We tried to establish the collagen-sandwich methods of primary rat hepatocyte culture, that is expected reflected more biological condition. However, collagen-sandwich methods was not suitable to treat the short-time changing. We decided to try the synchronization of cultured heptocyte via normal rat heptocyte culture. The synchronization was performed using 50% serum exposure, or high-dose insulin or dexametazone exposure and the samples were collect. We continue to analyze the mRNA expression.
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| Academic Significance and Societal Importance of the Research Achievements |
本研究ではコラーゲンサンドイッチ法による初代培養肝細胞の可能性を提示した。しかしながら、実際にmRNAを抽出したりタンパク質を抽出しての短期での変化を検討するには困難な手法であると判断した。培養細胞の概日リズム同期については検討中であるが、末梢臓器でしかも細胞単位での概日リズムは生体内では重要であるが注目はされずらく、今後検討を重ねる。
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