| Project/Area Number |
15K19902
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| Research Category |
Grant-in-Aid for Young Scientists (B)
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| Allocation Type | Multi-year Fund |
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| Research Field |
Digestive surgery
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| Research Institution | Fukushima Medical University |
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Principal Investigator |
SATO Naoya 福島県立医科大学, 医学部, 助教 (90622332)
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| Project Period (FY) |
2015-04-01 – 2017-03-31
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| Project Status |
Completed (Fiscal Year 2016)
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| Budget Amount *help |
¥3,900,000 (Direct Cost: ¥3,000,000、Indirect Cost: ¥900,000)
Fiscal Year 2016: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
Fiscal Year 2015: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
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| Keywords | 膵島移植 / Mitomycin-C / 生着延長 / 免疫抑制 / マイクロアレイ / サイトカイン / 免疫原性低下 / Mitomyciｎ-C |
|---|
| Outline of Final Research Achievements |
The purpose of this study to investigate a mechanism of islet graft engraftment by ex vivo mitomycin C (MMC) pretreatment, using comprehensive gene expression analysis of MMC-treated islets. The gene expression analysis identified significant downregulation of multiple genes encoding proinflammatory mediators with chemotactic activity, including multiple chemokines and peptidases. The result was validated by quantification of their proteins in islets culture supernatants. Moreover, we showed suppression of leukocyte-chemotactic activity of MMC-treated islets in vitro.
The ex vivo pretreatment of islets with MMC can reduce the immunogenic potential and prolong the survival of islet grafts by inducing the suppression of multiple leukocyte chemotactic factors.
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