2010 Fiscal Year Final Research Report
Studying mechanisms controlling responsiveness of Toll-like Receptors
Project/Area Number |
20390140
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Research Category |
Grant-in-Aid for Scientific Research (B)
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Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
Immunology
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Research Institution | The University of Tokyo |
Principal Investigator |
MIYAKE Kensuke The University of Tokyo, 医科学研究所, 教授 (60229812)
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Project Period (FY) |
2008 – 2010
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Keywords | 自然免疫 |
Research Abstract |
In the present study, we analyzed mechanisms regulating responsiveness of the Toll family of receptors. A variety of molecules are required for regulating TLR function. PRAT4A, e.g., is required for trafficking of cell surface TLRs from the ER to the cell surface. Unc93B1 is required for the trafficking of nucleic acid-sensing TLRs from the ER to the endolysosomes. Unc93B1 also has a role in balancing RNA-sensing TLR7 and DNA-sensing TLR9.
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Research Products
(13 results)
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[Journal Article] Unc93B1 restricts systemic lethal inflammation by orchestrating TLR7- and TLR9-trafficking.2011
Author(s)
Fukui R, Saitoh S-I, Kanno A, Onji M, Shibata T, Ito A, Onji M, Matsumoto M, Akira S, Yoshida N, Miyake K.
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Journal Title
Peer Reviewed
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[Journal Article] Tonic B cell activation by Radioprotective105/MD-1 promotes disease progression in MRL/lpr mice.2008
Author(s)
Kobayashi, T., K.Takahashi, Y.Nagai, T.Shibata, M.Otani, S.Izui, S.Akira, Y.Gotoh, H.Kiyono, *Miyake K
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Journal Title
Int.Immunol. 20
Pages: 881-891
Peer Reviewed
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