| Project/Area Number |
15590941
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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 |
Metabolomics
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| Research Institution | YAMAGUCHI UNIVERSITY |
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Principal Investigator |
MATSUBARA Atsushi Yamaguchi University, University Hospital, Assistant Professor, 医学部附属病院, 講師 (40311815)
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| Co-Investigator(Kenkyū-buntansha) |
TANIZAWA Yukio Yamaguchi University, Graduate School of Medicine, Professor, 医学部附属病院, 教授 (00217142)
UEDA Kohei Yamaguchi University, Health Service Center, Research Associate, 保健管理センター, 助手 (50325221)
TANABE Katsuya Yamaguchi University, University Hospital, Clinical Resident, 医学部附属病院, 医院(臨床)
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| Project Period (FY) |
2003 – 2004
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| Project Status |
Completed (Fiscal Year 2004)
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| Budget Amount *help |
¥3,500,000 (Direct Cost: ¥3,500,000)
Fiscal Year 2004: ¥1,600,000 (Direct Cost: ¥1,600,000)
Fiscal Year 2003: ¥1,900,000 (Direct Cost: ¥1,900,000)
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| Keywords | diabetes mellitus / islet beta cell / constitutive secretion / C-peptide / insulin / ELISA / 人工レポーター分子 / 膵β細胞 / インスリンプロモーター / モデルマウス |
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| Research Abstract |
To quantify the islet beta cell mass, we tried to develop the noninvasive and easily measurable system. We designed a beta cell model, which constitutively secrete an artificial reporter molecule, reflecting the beta cell mass, to be measured with conventional methods. First of all, we have constructed three types of artificial fusion proteins. One has the human albumin signal sequence with the human C-peptide (Alb-hc), another two types of constructs both have the mice IgK signal sequence fused with human C-peptide cDNA (hCPR tandem) while the one has also YFP cDNA (hCPR/YFP). We have determined those proteins expression and secretion outside of cultured cell lines (Cos7, HEK293), meaning these signal peptides play the role as the secreting signal in vivo. Besides we could detect and measure those fusion proteins with the human C-peptide ELISA kit, these reporter molecules are apparently easy to be measured.
As the further investigation, we will import those reporters into MIN6 cells, mouse beta cell line, and prove those expression in it and secretion. It is important to confirm whether those reporters secretion is constitutive or not. We have to determine the alteration of those reporters secretion independent of several conditions (glucose stimulation etc.) so that we will be able to use these reporters to calculate beta cell mass.
After establishing transgenic mice imported those fusion genes, we are making hybrid mice between these mice and other diabetic mice. These hybrid mice will demonstrate the alteration of beta cell mass till the onset of diabetes mellitus. Along with the elucidation of the mechanism of the diabetes onset or progression, this noninvasive beta cell mass quantifying system will contribute to developing the new drugs to inhibit beta cell mass reduction or to the advancing of beta cell regenerative therapy.
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