2017 Fiscal Year Final Research Report
Aquaporins involved with diabetes insipidus and the investigation of natural compounds controling the function of aquaporns
Project/Area Number |
26460223
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Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Multi-year Fund |
Section | 一般 |
Research Field |
Medical pharmacy
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Research Institution | Gifu Pharmaceutical University |
Principal Investigator |
|
Co-Investigator(Kenkyū-buntansha) |
大山 雅義 岐阜薬科大学, 薬学部, 教授 (30381718)
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Project Period (FY) |
2014-04-01 – 2018-03-31
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Keywords | アクアポリン / 細胞膜移行 / 細胞質移行 / プロテインキナーゼC / アクチン / 微小管 / Akt |
Outline of Final Research Achievements |
Aquaporins which are intrinsic membrane proteins functioning as a water channel permeable to water and glycerol. All aquaporin molecules expressing in cells do not always exist in a cell membrane, but the trafficking of aquaporins in a cell are controlled to move between the cell membrane and inside the cell as necessary. We found that the movement of aquaporin 3 from inside to membrane was regulated by protein kinase C and that from membrane to inside was done by protein kinase B (Akt). Phosphorylation of Thr237 and Ser275 in aquaporin 3 was confirmed to be necessary to move from inside the cell to cell membrane. We investigated natural compounds which triggered the trafficking of aquaporins. Eugenol which is a component of magnolia flower derived from Magnolia salicifolia was found to promote the trafficking of aquaporin 3 from inside to membrane accompanying the phosphorylation of protein kinase C.
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Free Research Field |
薬学 細胞生物学
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