Project/Area Number |
09102008
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Research Category |
Grant-in-Aid for Specially Promoted Research
|
Allocation Type | Single-year Grants |
Review Section |
Biological Sciences
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Research Institution | Tokyo Institute of Technology |
Principal Investigator |
HIROSE Shigehisa Tokyo Institute of Technology, Graduate School of Bioscience and Biotechnology, Professor, 大学院・生命理工学研究科, 教授 (10134199)
|
Co-Investigator(Kenkyū-buntansha) |
HAGIWARA Hiromi Tokyo Institute of Technology, Graduate School of Bioscience and Biotechnology, Assistant Professor, 大学院・生命理工学研究科, 助教授 (90189465)
TAKEI Yoshio University of Tokyo, Ocean Research Institute, Professor, 海洋研究所, 教授 (10129249)
|
Project Period (FY) |
1997 – 2001
|
Project Status |
Completed (Fiscal Year 2001)
|
Budget Amount *help |
¥157,600,000 (Direct Cost: ¥151,000,000、Indirect Cost: ¥6,600,000)
Fiscal Year 2001: ¥28,600,000 (Direct Cost: ¥22,000,000、Indirect Cost: ¥6,600,000)
Fiscal Year 2000: ¥21,000,000 (Direct Cost: ¥21,000,000)
Fiscal Year 1999: ¥21,000,000 (Direct Cost: ¥21,000,000)
Fiscal Year 1998: ¥30,000,000 (Direct Cost: ¥30,000,000)
Fiscal Year 1997: ¥57,000,000 (Direct Cost: ¥57,000,000)
|
Keywords | Osmoregulation / Natriuretic peptide / Chloride cell / Eel / Dace / Acid adaptation / K channel / ウグイ / クローディン / 内向き整流性Kチャネル / 恐山 / ANP受容体 / 海水適応 |
Research Abstract |
We used the comparative approach to gain insights into the complex regulatory system of the body fluid homeostasis by using animals with morphological and functional specializations such as the eel that can survive both in freshwater and seawater and the Osorezan dace that can live and grow in a pH 3.5 lake. (1) Through the analyses of both ligands and the corresponding receptors, we showed that the natriuretic peptide (NP) system is a key endocrine system that governs the euryhalinity of eel. NP is not only involved in quick regulation of various pre-existing transporters upon transfer to different salinities, but also stimulates secretion of cortisol and growth hormone, thereby being involved in long-term adaptation. We also identified NPs from diverse vertebrate species that perform unique osmoregulation such as sharks and hagfish to assess molecular evolution of the NP family. (2) Molecular mechanism of acid adaptation of the Osorezan dace was clarified by identifying ion transporters, channel, and their related molecules that become highly induced when dace are transferred from neutral to acidic water. Furthermore, the molecules responsible for the acid tolerance were mainly expressed in chloride cells. (3) Osmoregulation in teleost fish is achieved largely through active salt transport by specialized cells known as chloride cells. Reflecting their extraordinary power of ion transport, chloride cells are rich in Na, K-ATPase. Exploiting this unique property of the chloride cell, we succeeded in identifying a K channel likely to be functionally coupled with Na, K-ATPase ; identification of such a K channel has been a long-standing goal in animal physiology. (4) Autoradiographic localization of eel NP receptor revealed an unexpectedly dense localization in the gill chondrocytes, suggesting tight relationship between the NP system and bone metabolism, which then open a new avenue in the field of bone research.
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