Understanding for the induction mechanisms of intestinal IL22-producing cells
Project/Area Number |
26893326
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Research Category |
Grant-in-Aid for Research Activity Start-up
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Allocation Type | Single-year Grants |
Research Field |
Immunology
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Research Institution | Institute of Physical and Chemical Research |
Principal Investigator |
Tanoue Takeshi 国立研究開発法人理化学研究所, 統合生命医科学研究センター, 基礎科学特別研究員 (60732972)
|
Project Period (FY) |
2014-08-29 – 2016-03-31
|
Project Status |
Completed (Fiscal Year 2015)
|
Budget Amount *help |
¥2,730,000 (Direct Cost: ¥2,100,000、Indirect Cost: ¥630,000)
Fiscal Year 2015: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2014: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
|
Keywords | IL22 / 腸内細菌 / 腸内常在菌 / IL-22 |
Outline of Final Research Achievements |
In this study, I focused on interleukin (IL)22-producing cells, which are considered to be a key player in protection against gastrointestinal infection. First, I’ve analyzed the numbers of IL22-prodcing cells in various tissues of healthy mice. As a result, IL22-producing cells were abundant in gut, especially in the small intestine. In contrast to microbiota-harboring SPF (specific pathogen free) mice, germ-free mice showed substantially lower numbers of the cells, suggesting gut microbiota induce the accumulation of IL22-producing cells. Furthermore, I found that type3 innate lymphoid cells are main cellular source of IL22 and gram-positive ingenious members induce the IL22+ ILC3.
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Report
(3 results)
Research Products
(2 results)
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[Journal Article] Th17 Cell induction by adhesion of microbes to intestinal epithelial cells2015
Author(s)
Atarashi, K., Tanoue, T., Ando. M., Kamada, N., Nagano, Y., Narushima, S., Suda, W., Imaoka, A., Setoyama, H., Nagamori, T., Ishikawa, E., Shima, T., Hara, T., Kado, S., Jinnohara, T., Ohno, H., Kondo, T. et al.
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Journal Title
Cell
Volume: 163
Issue: 2
Pages: 367-380
DOI
Related Report
Peer Reviewed / Open Access / Int'l Joint Research
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