2005 Fiscal Year Final Research Report Summary
Regulation mechanisms of aquaporin in the brain and its functions in the brain edema
| Project/Area Number |
15591652
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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 |
Anesthesiology/Resuscitation studies
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| Research Institution | Nagoya City University |
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Principal Investigator |
KATSUYA Hirotada Nagoya City University, Graduate School of Medical Sciences, Professor, 大学院医学研究科, 教授 (20040561)
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| Co-Investigator(Kenkyū-buntansha) |
SOBUE Kazuya Nagoya City University, Graduate School of Medical Sciences, Assistant Professor, 大学院医学研究科, 講師 (90264738)
ASAI Kiyofumi Nagoya City University, Graduate School of Medical Sciences, Professor, 大学院医学研究科, 教授 (70212462)
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| Project Period (FY) |
2003 – 2005
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| Keywords | Brain edema / Aquaporin / Central nervous system / Astrocytes |
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| Research Abstract |
Aquaporins (AQPs) are water channel proteins, which increase water permeability via the plasma membrane and thus provide a route for rapid fluid movement. In the brain, AQP4 is abundantly expressed, and is highly concentrated in astrocyte membranes that are in direct contact with capillaries and pia. AQP4 is considered a major pathway for massive water shift across the plasma membrane under various conditions and is involved in brain edema formation. However, little is known concerning the mechanisms by which AQP4 expression is regulated in the brain. We investigated molecules, which interact with AQP4 and discovered RIL as a binding protein. Actually, it is confirmed that RIL directly interacted with AQP4 by in vitro binding assay, pull down assay, co-immunoprecipitation, and immunohistochemical staining. We are preparing a vector for a RIL null mouse, which reveals the regulation mechanisms of AQP4 by RIL. It is possible that RIL is a target molecule for a new therapeutic method of brain edema.
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