| Project/Area Number |
26670241
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| Research Category |
Grant-in-Aid for Challenging Exploratory Research
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| Allocation Type | Multi-year Fund |
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| Research Field |
Immunology
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| Research Institution | National Institutes of Biomedical Innovation, Health and Nutrition |
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Principal Investigator |
KUNISAWA Jun 国立研究開発法人医薬基盤・健康・栄養研究所, 医薬基盤研究所 ワクチンマテリアルプロジェクト, プロジェクトリーダー (80376615)
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| Project Period (FY) |
2014-04-01 – 2016-03-31
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| Project Status |
Completed (Fiscal Year 2015)
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| Budget Amount *help |
¥3,770,000 (Direct Cost: ¥2,900,000、Indirect Cost: ¥870,000)
Fiscal Year 2015: ¥2,210,000 (Direct Cost: ¥1,700,000、Indirect Cost: ¥510,000)
Fiscal Year 2014: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
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| Keywords | 免疫学 / 発生・分化 / メタボリズム / ビタミン |
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| Outline of Final Research Achievements |
It was demonstrated that in the intestinal IgA exhibits memory responses, but underlying mechanisms remain unclear. In this study, we performed metabolic analysis for energy metabolism that seems to be involved in the induction and maintenance of intestinal IgA responses. Naive B cells from the Peyer’s patches predominantly use TCA cycle, whereas IgA producing cells in the intestinal lamina propria shift their energy metabolism to glycolysis-initiated one. In agreement with these metabolic changes, naive B cells were dramatically reduced in mice lacking vitamin B1, an essential co-factor for the TCA cycle and intestinal IgA responses against oral vaccine were consequently impaired. These findings suggest that energy metabolism during B cell differentiation for intestinal IgA responses was changed, which is possibly associated with the induction and maintenance of intestinal IgA memory responses.
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