2015 Fiscal Year Final Research Report
Challenge for diabetes therapy based on understanding of stress signals in pancreatic islet niche
Project/Area Number |
25860759
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Research Category |
Grant-in-Aid for Young Scientists (B)
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Allocation Type | Multi-year Fund |
Research Field |
Metabolomics
|
Research Institution | Sasaki Foundation |
Principal Investigator |
Okita Naoyuki 公益財団法人佐々木研究所, 附属佐々木研究所, 研究員 (60453841)
|
Project Period (FY) |
2013-04-01 – 2016-03-31
|
Keywords | 膵島 / ストレス応答 |
Outline of Final Research Achievements |
Decline of pancreatic islet homeosotatsis by nutrient stress is involved in the pathogenesis of type2 diabetes mellitus. In the present study, I established the research basis for understanding the signal network of pancreatic islet failure focused on cell-cell interaction. I obtained the results as shown below: difference among chronic nutrient stresses in beta cell line: optimization of pseudoislet formation: construction of plasmid vectors that possess tetracylin-dependent gene regulatory system with cell marking system by fluorescence proteins: improved method of western blotting for Insulin and the other diabetes-associated peptide hormones.
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Free Research Field |
分子代謝制御学
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