The immunological analysis of MARCH I regulating IgE production
Project/Area Number |
24590466
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Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Multi-year Fund |
Section | 一般 |
Research Field |
Experimental pathology
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Research Institution | Gihu University of Medical Science (2013-2015) The Institute of Physical and Chemical Research (2012) |
Principal Investigator |
HOSHINO Mari 岐阜医療科学大学, 保健科学部, 教授 (10313511)
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Research Collaborator |
HOSHINO Katsuaki 香川大学, 医学部, 教授 (50324843)
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Project Period (FY) |
2012-04-01 – 2016-03-31
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Project Status |
Completed (Fiscal Year 2015)
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Budget Amount *help |
¥5,330,000 (Direct Cost: ¥4,100,000、Indirect Cost: ¥1,230,000)
Fiscal Year 2014: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2013: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2012: ¥2,210,000 (Direct Cost: ¥1,700,000、Indirect Cost: ¥510,000)
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Keywords | E3ユビキチンリガーゼ / IgE / ユビキチンリガーゼ / MHCクラスII |
Outline of Final Research Achievements |
Membrane-associated RING-CH I (MARCH-I) has been suggested as a E3 ubiquitin ligase for the regulation of immune system. In this study we observed lower antigen(Ag)-specific antibody responses, especially and drastically lower Ag-specific IgE responses and lower Ag-specific T cell responses when MARCH I deficient mice were systemically immunized, compared with control mice. Next, we showed that MARCH I deficiency in dendritic cells was important for the decrease of immune responses such as low IgE production. This study revealed that MARCH I might be responsible for susceptibility to infection.
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Report
(5 results)
Research Products
(6 results)
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[Journal Article] HSP90α deficiency does not affect Ig gene hypermutation and class switch but causes enhanced MHC class II antigen presentation2012
Author(s)
Li, Y., Li, S., Hoshino, M., Ishikawa, R., Kajiwara, C., Gao, X., Zhao, Y., Ishido, S., Udono, H., Wang, J. -Y.
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Journal Title
Int. Immunol.
Volume: 24
Issue: 12
Pages: 751-758
DOI
Related Report
Peer Reviewed
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