2012 Fiscal Year Final Research Report
Elucidating the physiological meaning of a novel TLR regulatory molecule
Project/Area Number |
23790526
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Research Category |
Grant-in-Aid for Young Scientists (B)
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Allocation Type | Multi-year Fund |
Research Field |
Immunology
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Research Institution | The University of Tokyo |
Principal Investigator |
SHIBATA Takuma 東京大学, 医科学研究所, 特任助教 (30554505)
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Project Period (FY) |
2011 – 2012
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Keywords | 自然免疫 / TLR |
Research Abstract |
We identified a novel TLR associating molecule, Epithelial membrane protein (Emp3), and found that knock-down of Emp3 in RAW macrophage cell line resulted in upregulation of multiple TLR response. However, bone marrow derived macrophages from Emp3 KO and Emp3 Tg mice did not show clear differences in various types of TLR response. On the other hand, Emp3 Tg mice died within 6 months and most of them showed Dilated Cardiomyopathy (DCM) like heart symptoms. In addition, some Emp3 Tg mice showed enteritis. It still remained to be determined whether thesephenotypes are associated with unknown TLR function regulated by Emp3 or not.
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[Journal Article] PRAT4A-dependent expression of cell surface TLR5 on neutrophils, classical monocytes and dendritic cells.2012
Author(s)
Shibata T, Takemura N, Motoi Y, Goto Y,Karuppuchamy T, Izawa K, Li X,Akashi-Takamura S, Tanimura N, Kunisawa J,Kiyono H, Akira S, Kitamura T, Kitaura J, Uematsu S, Miyake K.
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Journal Title
International Immunology
Volume: 24巻,10号
Pages: 613-23
DOI
Peer Reviewed
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