Visualization and molecular analysis of antigen-uptake and -delivery at M cell.
Project/Area Number |
21790487
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Research Category |
Grant-in-Aid for Young Scientists (B)
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Allocation Type | Single-year Grants |
Research Field |
Immunology
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Research Institution | The Institute of Physical and Chemical Research |
Principal Investigator |
KIMURA Shunsuke The Institute of Physical and Chemical Research, 大学院・医学研究科, 助教 (40444525)
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Project Period (FY) |
2009 – 2010
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Project Status |
Completed (Fiscal Year 2010)
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Budget Amount *help |
¥4,290,000 (Direct Cost: ¥3,300,000、Indirect Cost: ¥990,000)
Fiscal Year 2010: ¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
Fiscal Year 2009: ¥2,210,000 (Direct Cost: ¥1,700,000、Indirect Cost: ¥510,000)
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Keywords | パイエル板 / M細胞 / CCR1 / CCL9 / 形質細胞 / pDC |
Research Abstract |
Peyer's patch (PP) in the small intestine is a primary site for the intestinal immune system. The luminal side of PPs is covered by the follicle-associated epithelium (FAE), which contains M cells. M-cells uptake antigens or macromolecules and deliver them to dendritic cells inhabiting subepithelial dome region under FAE. We found high expression level of a chemokine gene, Ccl9, in the M cells by using the mouse chemokine array and in situ hybridization analysis. The cells expressing CCR1 protein, a receptor of CCL9, were found underneath M cells and close contact with. Moreover, M cells expressed a gene of M-Sec which product is a key molecule of the formation of membrane nanotubes, a new structure for cell-cell communication. Taken together, our data suggest that M cells interact and communicate with immune cells by two ways, CCL9-CCR1 and membrane nanotubes.
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Report
(3 results)
Research Products
(14 results)
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[Journal Article] The epithelia-specific membrane trafficking factor AP-1B secures gut immune homeostasis in mice.2011
Author(s)
Takahashi D, Hase K, Kimura S, Nakatsu F, Ohmae M, Mandai Y, Sato T, Date Y, Ebisawa M, Kato T, Obata Y, Fukuda S, Kawamura Y, Dohi D, Katsuno T, Yokosuka O, Waguri S, Ohno H
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Journal Title
Related Report
Peer Reviewed
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[Journal Article] M-Sec promotes membrane nanotube formation by interacting with Ral and the exocyst complex.2009
Author(s)
Hase K, Kimura S, Takatsu H, Ohmae M, Kawano S, Kitamura H, Ito M, Watarai H, Hazelett CC, Yeaman C, Ohno H.
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Journal Title
Nat Cell Biol 11(12)
Pages: 1427-1432
Related Report
Peer Reviewed
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[Journal Article] Uptake through glycoprotein 2 of FimH(+) bacteria by M cells initiates mucosal immune response.2009
Author(s)
Hase K, Kawano K, Nochi T, Pontes GS, Fukuda S, Ebisawa M, Kadokura K, Tobe T, Fujimura Y, Kawano S, Yabashi A, Waguri S, Nakato G, Kimura S, Murakami T, Iimura M, Hamura K, Fukuoka S, Lowe AW, Itoh K, Kiyono H, Ohno H.
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Journal Title
Nature 462(7270)
Pages: 226-230
Related Report
Peer Reviewed
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[Journal Article] M-Sec promotes membrane nanotube formation by interacting with Ral and the exocyst complex2009
Author(s)
Hase K, Kimura S, Takatsu H, Ohmae M, Kawano S, Kitamura H, Ito M, Watarai H, Hazelett CC, Yeaman C, Ohno H
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Journal Title
Nat Cell Biol 11
Pages: 1427-32
Related Report
Peer Reviewed
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[Journal Article] Uptake through glycoprotein 2 of FimH(+)bacteria by M cells initiates mucosal immune response2009
Author(s)
Hase K, Kawano K, Nochi T, Pontes GS, Fukuda S, Ebisawa M, Kadokura K, Tobe T, Fujimura Y, Kawano S, Yabashi A, Waguri S, Nakato G, Kimura S, Murakami T, Iimura M, Hamura K, Fukuoka S, Lowe AW, Itoh K, Kiyono H, Ohno H.
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Journal Title
Related Report
Peer Reviewed
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[Presentation]2009
Author(s)
Shunsuke Kimura, Ayako Sakamoto, Ryo Yamazaki, Kazuya Kawano, Koji Hase, Hiroshi Ohno
Organizer
日本細胞生物学会
Place of Presentation
愛知県名古屋市
Year and Date
2009-06-02
Related Report
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